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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">abcic</journal-id>
      <journal-title-group>
        <journal-title>ABC Imagem Cardiovascular</journal-title>
        <abbrev-journal-title abbrev-type="publisher">ABC Imagem Cardiovasc.</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2675-312X</issn>
      <issn pub-type="ppub">2318-8219</issn>
      <publisher>
        <publisher-name>Departamento de Imagem Cardiovascular da Sociedade Brasileira de Cardiolodia (DIC/SBC)</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id specific-use="scielo-v3" pub-id-type="publisher-id">76YYGgFRyqPShtkmnXvH3xB</article-id>
      <article-id specific-use="scielo-v2" pub-id-type="publisher-id">S2675-312X2026000101407</article-id>
      <article-id pub-id-type="other">01407</article-id>
      <article-id pub-id-type="doi">10.36660/abcimg.20260016i</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Review Article</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>The Use of Artificial Intelligence in the Diagnosis of Cardiac Amyloidosis: Integrative Review</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-2331-6871</contrib-id>
          <name>
            <surname>Lemos</surname>
            <given-names>Nilson Batista</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
          <xref ref-type="corresp" rid="c1"/>
          <role>Conception and design of the research</role>
          <role>analysis and interpretation of the data</role>
          <role>writing of the manuscript and critical revision of the manuscript for intellectual content</role>
          <role>obtaining financing</role>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0009-0006-1640-0975</contrib-id>
          <name>
            <surname>Ara&#250;jo</surname>
            <given-names>Gabriela Aparecida Moreira</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
          <role>Conception and design of the research</role>
          <role>analysis and interpretation of the data</role>
          <role>writing of the manuscript and critical revision of the manuscript for intellectual content</role>
          <role>obtaining financing</role>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0001-8809-8783</contrib-id>
          <name>
            <surname>Melo</surname>
            <given-names>Marcelo Dantas Tavares de</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
          <role>Conception and design of the research</role>
          <role>analysis and interpretation of the data</role>
          <role>writing of the manuscript and critical revision of the manuscript for intellectual content</role>
        </contrib>
        <aff id="aff1">
          <label>1</label>
          <institution content-type="orgname">Universidade Federal da Para&#237;ba</institution>
          <addr-line>
            <named-content content-type="city">Jo&#227;o Pessoa</named-content>
            <named-content content-type="state">PB</named-content>
          </addr-line>
          <country country="BR">Brazil</country>
          <institution content-type="original">Universidade Federal da Para&#237;ba, Jo&#227;o Pessoa, PB &#8211; Brazil</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c1"><label>Correspond&#234;ncia:</label><bold>Nilson Batista Lemos</bold> &#8226; Universidade Federal da Para&#237;ba. Campus I Lot., Cidade Universitaria. CEP: <postal-code>58051-900</postal-code>. Jo&#227;o Pessoa, PB &#8211; Brasil E-mail: <email>nilsonlemos18@gmail.com</email> </corresp>
        <fn fn-type="coi-statement">
          <label>Potential Conflict of Interest</label>
          <p>No potential conflict of interest relevant to this article was reported.</p>
        </fn>
        <fn fn-type="edited-by">
          <label>Editor respons&#225;vel pela revis&#227;o:</label>
          <p>Marcelo Tavares</p>
        </fn>
      </author-notes>
      <pub-date date-type="pub" publication-format="electronic">
        <day>25</day>
        <month>05</month>
        <year>2026</year>
      </pub-date>
      <pub-date date-type="collection" publication-format="electronic">
        <year>2026</year>
      </pub-date>
      <volume>39</volume>
      <issue>1</issue>
      <elocation-id>e20260016</elocation-id>
      <history>
        <date date-type="received">
          <day>08</day>
          <month>02</month>
          <year>2026</year>
        </date>
        <date date-type="rev-recd">
          <day>09</day>
          <month>02</month>
          <year>2026</year>
        </date>
        <date date-type="accepted">
          <day>09</day>
          <month>02</month>
          <year>2026</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/" xml:lang="en">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License</license-p>
        </license>
      </permissions>
      <abstract>
        <title>Abstract</title>
        <sec>
          <title>Fundamento:</title>
          <p>Cardiac amyloidosis is a rare form of infiltrative cardiomyopathy characterized by the deposition of proteins in the myocardium, resulting in increased wall thickness, impaired ventricular function, and possible progression to heart failure. Diagnosis is challenging due to the low prevalence of the disease and the nonspecific nature of its clinical manifestations. The application of artificial intelligence (AI) to the analysis of medical tests emerges as a promising strategy for early detection, more accurate diagnosis, and timely initiation of treatment.</p>
        </sec>
        <sec>
          <title>Methods:</title>
          <p>An integrative literature review was conducted on the use of AI in the diagnosis of cardiac amyloidosis. Articles published between 2019 and 2024 were searched in the PubMed, Scopus, Web of Science, Embase, and Cochrane Library databases.</p>
        </sec>
        <sec>
          <title>Results:</title>
          <p>Of the 420 articles initially identified, 21 met the eligibility criteria and were included in the final analysis. A predominance of retrospective observational studies applying machine learning models was observed. Among the diagnostic modalities evaluated in association with AI, electrocardiography and echocardiography were the most frequently studied tests.</p>
        </sec>
        <sec>
          <title>Conclusion:</title>
          <p>AI demonstrates high potential to improve the screening and diagnosis of cardiac amyloidosis when applied to the analysis of clinical and imaging tests. The findings of this review indicate that AI may accelerate the diagnostic process, reduce the need for invasive procedures, and optimize the use of health care resources. However, to expand its integration into clinical practice and enhance its generalizability, further model refinement and validation in more diverse populations are required.</p>
        </sec>
      </abstract>
      <kwd-group xml:lang="en">
        <title>Keywords:</title>
        <kwd>Amyloidosis</kwd>
        <kwd>Artificial Intelligence</kwd>
        <kwd>Diagnosis</kwd>
      </kwd-group>
      <funding-group>
        <funding-statement><bold>Sources of Funding</bold>: There were no external funding sources for this study.</funding-statement>
      </funding-group>
      <counts>
        <fig-count count="4"/>
        <table-count count="2"/>
        <equation-count count="0"/>
        <ref-count count="21"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec sec-type="intro">
      <title>Introduction</title>
      <p>Amyloidosis is a generic term used to describe the extracellular deposition of fibrils formed by low-molecular-weight protein subunits derived from different precursor proteins. Amyloid deposits may result in a wide variety of clinical manifestations, which vary according to the type of protein involved, the amount deposited, and the tissue location. In the genesis of these deposits, initially soluble peptides undergo conformational changes, predominantly acquiring an antiparallel beta-pleated sheet structure, which favors their stacking into twisted fibrils.<sup><xref ref-type="bibr" rid="B1">1</xref></sup></p>
      <p>There are dozens of systemic and localized forms of amyloidosis. Among them, four precursor proteins may give rise to both localized and systemic deposits. The main systemic forms are immunoglobulin light-chain (AL) amyloidosis and (ATTR) transthyretin amyloidosis. These forms are named according to the precursor protein of the amyloid deposit (AL or ATTR) and account for approximately 95% of cases of cardiac amyloidosis. The remaining forms correspond to other subtypes of amyloidosis, which are also clinically relevant.<sup><xref ref-type="bibr" rid="B2">2</xref>,<xref ref-type="bibr" rid="B3">3</xref></sup></p>
      <p>ATTR amyloidosis is characterized by the misfolding and subsequent deposition of transthyretin, a protein responsible for the transport of thyroid hormone and vitamin A. It may present in wild-type or hereditary form.<sup><xref ref-type="bibr" rid="B2">2</xref>-<xref ref-type="bibr" rid="B4">4</xref></sup> Similarly, AL amyloidosis results from the accumulation of misfolded immunoglobulin light chains produced by plasma cells associated with dyscrasias.<sup><xref ref-type="bibr" rid="B2">2</xref>,<xref ref-type="bibr" rid="B3">3</xref></sup></p>
      <p>In cardiac amyloidosis, it is a rare form of progressive cardiomyopathy whose population prevalence has not yet been well established.<sup><xref ref-type="bibr" rid="B5">5</xref></sup> The disease is caused by myocardial deposition of misfolded amyloid proteins, resulting in restrictive cardiomyopathy, with possible progression to heart failure, conduction system disorders, and cardiac death.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B6">6</xref></sup> It may present with cardiovascular signs and symptoms or be diagnosed during the investigation of extracardiac manifestations of the disease.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B6">6</xref>,<xref ref-type="bibr" rid="B7">7</xref></sup> Due to its heterogeneous clinical phenotype and frequently nonspecific manifestations, diagnosis and management tend to occur late.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B6">6</xref></sup></p>
      <fig id="f1">
        <graphic xlink:href="2675-312X-abcic-39-01-e20260016-0016i-gf01.tif"/></fig>
      <p>With regard to the diagnostic approach to cardiac amyloidosis, it is essential to recognize clinical scenarios and abnormalities in complementary tests that indicate the need for investigation. However, diagnosis is challenging, especially because it is often an indolent disease whose symptoms may overlap with those of more prevalent heart diseases.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B5">5</xref></sup> Depending on the clinical context and resource availability, various tools may be employed, including electrocardiography (ECG), echocardiography, cardiac magnetic resonance (CMR), bone-seeking tracers scintigraphy, monoclonal protein screening by immunofixation, and biopsy of the affected tissue. Each method has its own characteristics and different levels of diagnostic accuracy (Central Illustration).</p>
      <p>Some findings may increase clinical suspicion of cardiac amyloidosis, such as discordance between increased left ventricular (LV) wall thickness and low QRS voltage, unexplained LV hypertrophy, low-flow, low-gradient aortic stenosis, relative apical sparing of longitudinal strain, a diffuse circumferential subendocardial late gadolinium enhancement pattern of the LV on CMR, and myocardial uptake of bone tracers on bone-seeking tracers scintigraphy.</p>
      <p>Despite the diversity of available diagnostic methods, cardiac amyloidosis remains underdiagnosed,<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B5">5</xref>-<xref ref-type="bibr" rid="B7">7</xref></sup> which has important repercussions for patients&#8217; quality of life. At the same time, the development of therapies capable of improving clinical outcomes has driven the search for strategies to increase diagnostic rates. These interventions may reduce or stabilize protein deposition, with a consequent reduction in the relative risk of hospitalizations, morbidity, and mortality associated with the disease.</p>
      <p>Because of the need for early detection of cardiac amyloidosis, the development of mechanisms that optimize screening and diagnosis with lower costs and risks is essential.<sup><xref ref-type="bibr" rid="B3">3</xref></sup> This review aims to present the main advances in disease detection, with emphasis on promising technological tools in diagnostic medicine, especially artificial intelligence (AI).</p>
      <p>AI is a branch of computer science dedicated to the development of systems capable of performing tasks that simulate human cognitive functions, such as decision-making and complex reasoning. In the field of medical diagnosis, these systems are trained using machine learning techniques, in which large volumes of data, often images, are used for pattern recognition. Among the most commonly employed approaches are convolutional neural networks (CNNs), which consist of multiple layers that extract progressively more complex features from the analyzed data, enabling automated identification of patterns in images and other types of information. In general, the larger and more representative the dataset used for training, the greater the model's accuracy tends to be.</p>
      <p>Incorporating AI into medical practice enables the more effective screening of rare diseases and improves diagnostic accuracy. AI appears particularly promising for rare diseases that are often underrecognized in clinical practice. Automated systems can integrate multiple signs, symptoms, and complementary findings, helping to guide clinical reasoning. Thus, core skills in medicine, such as pattern recognition, are increasingly being incorporated into computational models with the aim of enhancing diagnostic reliability and supporting decision-making in everyday medical practice.</p>
      <p>Several studies have investigated the applicability of AI in the early diagnosis of cardiac amyloidosis. Among the most recent approaches are the integration of AI with imaging methods, such as positron emission tomography (PET-CT), bone-seeking tracers scintigraphy, and CMR as well as its application to the automated analysis of ECGs, genetic data, and phenotypic profiles of cardiac abnormalities. These aspects will be discussed throughout this review.</p>
    </sec>
    <sec sec-type="methods">
      <title>Methods</title>
      <p>The present study is characterized as an integrative literature review aimed at critically analyzing the use of AI in the diagnosis of cardiac amyloidosis. The review was conducted following six methodological steps: i) definition of the research question; ii) establishment of inclusion criteria and sample selection; iii) identification of preselected and selected studies; iv) organization and representation of the included studies; v) critical analysis of the data; and vi) synthesis of the available knowledge.</p>
      <p>Searches were conducted in the PubMed, Scopus, Web of Science, Embase, and Cochrane Library databases. The search strategy was developed using the descriptors "artificial intelligence," "amyloidosis," and "diagnosis," included in the Medical Subject Headings and Embase Subject Headings, combined using the Boolean operator AND.</p>
      <p>Original studies and meta-analyses published between 2019 and 2024 that evaluated the application of AI in the diagnosis of cardiac amyloidosis were included. Articles that did not meet the inclusion criteria were excluded, as well as narrative reviews, case reports, editorials, and studies with methodology considered inadequate.</p>
      <p>After article selection, methodological quality was assessed to ensure greater rigor in the interpretation of findings and robustness of the conclusions. For this step, the JBI critical appraisal tool was used, which includes specific criteria according to study design, covering aspects related to the sample, methodology, data analysis, bias control, and ethical considerations. Quality classification is based on the proportion of affirmative responses to the evaluated criteria, allowing comparison across studies and critical analysis of their results.</p>
    </sec>
    <sec sec-type="results">
      <title>Results</title>
      <p>The search strategy yielded 420 articles, distributed as follows: 124 identified in PubMed, 61 in Web of Science, 84 in Scopus, 147 in Embase, and 4 in the Cochrane Library. After removal of 192 duplicate studies, 228 articles remained for screening.</p>
      <p>Title and abstract screening resulted in the selection of 43 studies for full-text evaluation. After application of the eligibility criteria, 21 articles were included in the final analysis (<xref ref-type="fig" rid="f2">Figure 1</xref>).</p>
      <fig id="f2">
        <label>Figure 1</label>
        <caption>
          <title>Flowchart of the study selection process for the studies included in the integrative review.</title>
        </caption>
        <graphic xlink:href="2675-312X-abcic-39-01-e20260016-0016i-gf02.tif"/></fig>
      <p>Regarding methodological assessment according to the JBI criteria, most studies were classified as having good to excellent methodological quality, with scores ranging from 6 to 8 points. The main factors contributing to this classification included the use of robust statistical metrics and the application of cross-validation in the developed AI models.</p>
      <p>As limitations, the absence of gold-standard diagnostic confirmation of cardiac amyloidosis in part of the studies was observed, as well as the lack of external validation of the proposed models, which limits the generalizability of the findings. The detailed results of the methodological assessment are presented in <xref ref-type="table" rid="t1">Table 1</xref>.</p>
      <table-wrap id="t1">
        <label>Table 1</label>
        <caption>
          <title>Methodological characteristics and quality assessment of the included studies</title>
        </caption>
        <table frame="hsides" rules="groups">
          <colgroup width="20%">
            <col/>
            <col/>
            <col/>
            <col/>
            <col/>
          </colgroup>
          <thead style="border-top: thin solid; border-bottom: thin solid; border-color: #000000">
            <tr style="background-color:#C58874">
              <th align="left" valign="middle">No.</th>
              <th align="center" valign="middle">Study (author/year)</th>
              <th align="center" valign="middle">Design</th>
              <th align="center" valign="middle">Score (JBI/8)</th>
              <th align="center" valign="middle">Methodological assessment</th>
            </tr>
          </thead>
          <tbody style="border-bottom: thin solid; border-color: #000000">
            <tr>
              <td align="left" valign="middle">1</td>
              <td align="center" valign="middle">Agibetov et al. (2021)</td>
              <td align="center" valign="middle">Retrospective observational study with cardiac magnetic resonance and application of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">2</td>
              <td align="center" valign="middle">Barbieri et al. (2024)</td>
              <td align="center" valign="middle">Study with automated three-dimensional transthoracic echocardiography associated with machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr>
              <td align="left" valign="middle">3</td>
              <td align="center" valign="middle">Casta&#241;o et al. (2024)</td>
              <td align="center" valign="middle">Retrospective case-control observational study with application of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">4</td>
              <td align="center" valign="middle">Cotella et al. (2023)</td>
              <td align="center" valign="middle">Retrospective observational study with echocardiography and application of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr>
              <td align="left" valign="middle">5</td>
              <td align="center" valign="middle">Delbarre et al. (2023)</td>
              <td align="center" valign="middle">Multicenter retrospective observational study with bone-seeking tracers scintigraphy analyzed by machine learning</td>
              <td align="center" valign="middle">8</td>
              <td align="center" valign="middle">Excellent</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">6</td>
              <td align="center" valign="middle">Eckstein et al. (2022)</td>
              <td align="center" valign="middle">Observational cohort study with echocardiography and use of machine learning</td>
              <td align="center" valign="middle">6</td>
              <td align="center" valign="middle">Good quality</td>
            </tr>
            <tr>
              <td align="left" valign="middle">7</td>
              <td align="center" valign="middle">Garofalo et al. (2021)</td>
              <td align="center" valign="middle">Predictive computational study with experimental validation focused on genetic assessment using machine learning</td>
              <td align="center" valign="middle">6</td>
              <td align="center" valign="middle">Good quality</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">8</td>
              <td align="center" valign="middle">Goto et al. (2021)</td>
              <td align="center" valign="middle">Multicenter observational study using electrocardiography and echocardiography</td>
              <td align="center" valign="middle">8</td>
              <td align="center" valign="middle">Excellent</td>
            </tr>
            <tr>
              <td align="left" valign="middle">9</td>
              <td align="center" valign="middle">Harmon et al. (2023)</td>
              <td align="center" valign="middle">Retrospective observational study with electrocardiography and application of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">10</td>
              <td align="center" valign="middle">Huda et al. (2021)</td>
              <td align="center" valign="middle">Retrospective observational study with application of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr>
              <td align="left" valign="middle">11</td>
              <td align="center" valign="middle">Ma et al. (2024)</td>
              <td align="center" valign="middle">Retrospective observational study with non-contrast cardiac magnetic resonance and use of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">12</td>
              <td align="center" valign="middle">Martini et al. (2020)</td>
              <td align="center" valign="middle">Prospective observational study with cardiac magnetic resonance and application of machine learning</td>
              <td align="center" valign="middle">8</td>
              <td align="center" valign="middle">Excellent</td>
            </tr>
            <tr>
              <td align="left" valign="middle">13</td>
              <td align="center" valign="middle">Miller et al. (2024)</td>
              <td align="center" valign="middle">Retrospective observational study with positron emission tomography and automated segmentation</td>
              <td align="center" valign="middle">8</td>
              <td align="center" valign="middle">Excellent</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">14</td>
              <td align="center" valign="middle">Nowak et al. (2024)</td>
              <td align="center" valign="middle">Retrospective observational study with cardiac magnetic resonance, T1 mapping, and use of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr>
              <td align="left" valign="middle">15</td>
              <td align="center" valign="middle">Santarelli et al. (2020)</td>
              <td align="center" valign="middle">Prospective observational study with positron emission tomography and application of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">16</td>
              <td align="center" valign="middle">Schrutka et al. (2021)</td>
              <td align="center" valign="middle">Prospective case-control observational study with application of machine learning</td>
              <td align="center" valign="middle">6</td>
              <td align="center" valign="middle">Good quality</td>
            </tr>
            <tr>
              <td align="left" valign="middle">17</td>
              <td align="center" valign="middle">Shiri et al. (2024)</td>
              <td align="center" valign="middle">Prospective single-cohort observational study with application of machine learning</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">18</td>
              <td align="center" valign="middle">Spielvogel et al. (2024)</td>
              <td align="center" valign="middle">Multicenter retrospective observational study with bone-seeking tracers scintigraphy and use of machine learning</td>
              <td align="center" valign="middle">8</td>
              <td align="center" valign="middle">Excellent</td>
            </tr>
            <tr>
              <td align="left" valign="middle">19</td>
              <td align="center" valign="middle">Vrudhula et al. (2024)</td>
              <td align="center" valign="middle">Retrospective observational study with application of machine learning</td>
              <td align="center" valign="middle">6</td>
              <td align="center" valign="middle">Good quality</td>
            </tr>
            <tr style="background-color:#E8CCBF">
              <td align="left" valign="middle">20</td>
              <td align="center" valign="middle">Yang et al. (2024)</td>
              <td align="center" valign="middle">Observational study with digital histopathological analysis using a neural network and autofluorescence</td>
              <td align="center" valign="middle">7</td>
              <td align="center" valign="middle">High quality</td>
            </tr>
            <tr>
              <td align="left" valign="middle">21</td>
              <td align="center" valign="middle">Zhang et al. (2023)</td>
              <td align="center" valign="middle">Retrospective observational study with echocardiography and application of machine learning</td>
              <td align="center" valign="middle">6</td>
              <td align="center" valign="middle">Good quality</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
    </sec>
    <sec sec-type="discussion">
      <title>Discussion</title>
      <p>The use of AI as a supportive tool in the diagnosis of rare diseases, such as cardiac amyloidosis, has been considered promising, especially in the context of conditions with high clinical heterogeneity and that are frequently underrecognized by general practitioners. Early identification of the disease may modify its natural history and improve prognosis. This review sought to emphasize the potential of already established diagnostic tools for the evaluation of cardiac amyloidosis when combined with machine learning-based systems, an approach addressed in all included studies.</p>
      <p>To organize the analysis of the findings, AI performance will be discussed according to the different diagnostic modalities used in the screening and evaluation of cardiac amyloidosis.</p>
      <sec>
        <title>Performance of artificial intelligence in the evaluation of medical record data and laboratory tests</title>
        <p>Among the screening strategies for amyloid cardiomyopathy, the use of data extracted from electronic health records of patients with heart failure (HF) with preserved ejection fraction (HFpEF) stands out. To differentiate amyloid etiology, especially wild-type ATTR amyloidosis (ATTRwt), from non-amyloid etiology, Huda et al.<sup><xref ref-type="bibr" rid="B8">8</xref></sup> collected electronic health record data and developed an AI model capable of screening and identifying patients with ATTRwt amyloidosis. The system achieved an area under the receiver operating characteristic curve (AUC) of 0.80. Performance was supported by the identification of comorbidities more prevalent in the amyloid etiology group, such as atrial fibrillation and chronic kidney disease, and in the non-amyloid group, such as hypertension, diabetes mellitus, obesity, and coronary artery disease, which were used as predictive variables.</p>
        <p>Subsequently, Casta&#241;o et al.<sup><xref ref-type="bibr" rid="B9">9</xref></sup> refined the model by focusing the analysis on 11 main phenotypes associated with cardiac amyloidosis, including carpal tunnel syndrome and arrhythmias. The model demonstrated accuracy (74%), sensitivity (77%), and specificity (72%), with an AUC of 0.82. Although there was a slight reduction in some performance parameters, the model was simplified in terms of programming, facilitating its implementation in hospital settings and expanding its potential for population screening.</p>
        <p>The studies by Huda et al.<sup><xref ref-type="bibr" rid="B8">8</xref></sup> and Casta&#241;o et al.<sup><xref ref-type="bibr" rid="B9">9</xref></sup> demonstrate the feasibility of automated screening through systematic extraction of clinical data, a process that would be costly and operationally complex if performed manually. Although such models are limited by the quality of records coded according to the International Classification of Diseases and by the documented phenotypes, without direct integration of laboratory or imaging tests for definitive typing, they represent relevant tools for large-scale screening, directing patients with higher probability toward further investigation.</p>
        <p>Additionally, phenotypes recognized by the model, such as carpal tunnel syndrome, may precede the development of HF, which suggests a potential application of AI in preclinical stages, with implications for early identification of ATTR amyloidosis.</p>
      </sec>
      <sec>
        <title>Performance of artificial intelligence in electrocardiographic evaluation</title>
        <p>The application of AI in ECG analysis has emerged as a screening strategy, considering that ECG is a widely available, low-cost, noninvasive test.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B5">5</xref></sup> Model validation represents a fundamental step in the development of these tools, as it involves testing multiple variables across different populations.<sup><xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B6">6</xref></sup></p>
        <p>Harmon et al.<sup><xref ref-type="bibr" rid="B10">10</xref></sup> developed an algorithm applicable to diverse populations, including different races and sexes. The model achieved an AUC of 0.84 (95% CI: 0.82-0.86), maintaining consistent performance across subgroups, except in the Hispanic population, possibly underrepresented in the sample. The algorithm performed better in ECGs with low voltage and patterns compatible with prior infarction, and showed lower performance in left bundle branch block and LV hypertrophy. These findings suggest the need for greater sample diversity, without invalidating the use of the tool as a screening method.</p>
        <p>Vrudhula et al.<sup><xref ref-type="bibr" rid="B5">5</xref></sup> evaluated approximately 1.3 million ECGs from 341,989 patients. The different tested models showed AUC values ranging from 0.660 (95% CI: 0.642-0.736) to 0.898 (95% CI: 0.868-0.924), demonstrating relevant potential for screening and referral for further investigation. However, because of the rarity and underdiagnosis of cardiac amyloidosis, models are often trained with a limited number of confirmed cases.</p>
        <p>Similarly, Goto et al.<sup><xref ref-type="bibr" rid="B3">3</xref></sup> reported strong performance, with a C-statistic of 0.91 (95% CI: 0.90-0.93) in the Brigham and Women's Hospital test set, 0.85 (0.82-0.87) at Massachusetts General Hospital, and 0.86 (0.83-0.88) at the University of California, San Francisco. However, the authors emphasize that isolated ECG features do not provide sufficient sensitivity or specificity to be used as independent heuristics, and their integration with other clinical and diagnostic variables is recommended to optimize model performance.</p>
        <p>Schrutka et al.<sup><xref ref-type="bibr" rid="B6">6</xref></sup> also reinforce that the proposed model may assist in raising suspicion of cardiac amyloidosis even in the absence of advanced imaging methods. In that study, 20 patients with transthyretin cardiac amyloidosis, 11 with HFpEF, 30 with cardiac amyloidosis, and 50 with other HF etiologies were evaluated. The presence of a low-voltage ECG pattern associated with increased LV wall thickness was highly suggestive of cardiac amyloidosis, allowing differentiation from hypertensive or hypertrophic cardiomyopathy. In the analysis of ECG patterns, pattern 1 was present in 78% of patients with AL amyloidosis and in 58% of those with ATTR amyloidosis (p = 0.009), whereas pattern 2 was identified in 7% of AL amyloidosis cases and in 23% of ATTR amyloidosis cases (p = 0.006). The absence of a specific pattern was observed in 16% of patients with AL amyloidosis and in 18% of patients with ATTR amyloidosis (p = 0.620).</p>
      </sec>
      <sec>
        <title>Performance of artificial intelligence in echocardiographic evaluation</title>
        <p>Considering the versatility of echocardiography and its central role in the diagnostic investigation of cardiac amyloidosis, the development of AI models capable of reducing operational variability and improving diagnostic accuracy is highly relevant.</p>
        <p>Xiaofeng Zhang et al.<sup><xref ref-type="bibr" rid="B1">1</xref></sup> observed that there are still few studies on echocardiography-based myocardial texture analysis and that human visual assessment has limitations in characterizing these alterations. Based on transthoracic echocardiograms, the authors developed four machine learning algorithms to differentiate cardiac amyloidosis from other cardiomyopathies: random forest (RF), support vector machine (SVM), logistic regression (LR), and gradient boosting decision trees (GBDT).</p>
        <p>In the analyzed population, all models were able to effectively distinguish cases of cardiac amyloidosis from non-amyloid diseases. The LR model demonstrated the best diagnostic performance, outperforming the traditional ultrasonographic method (AUC: RF 0.77; SVM 0.81; LR 0.81; GBDT 0.71). The authors therefore proposed the application of this tool as a noninvasive diagnostic method for myocardial amyloidosis. However, the relatively small number of cardiac amyloidosis cases may have limited the model's sensitivity for discrimination between groups.</p>
        <p>Cotella et al.<sup><xref ref-type="bibr" rid="B2">2</xref></sup> developed an AI model focused on the automated assessment of LV ejection fraction (LVEF) and global longitudinal strain (GLS), central parameters in the diagnosis of cardiac amyloidosis. The authors justified the incorporation of AI based on the fact that manual measurements are time-consuming and show significant inter- and intraobserver variability, which may compromise diagnostic accuracy and influence therapeutic decisions. The study demonstrated that automated and quantitative measurements of LVEF and GLS showed high accuracy and enabled sensitive and specific detection of abnormalities when compared with conventional manual analysis, both in examinations performed before the diagnosis of cardiac amyloidosis and at the time of diagnosis. No statistically significant differences were observed between values obtained by the two methods in the prediagnostic period (LVEF: p = 0.791; GLS: p = 0.105) or at the time of diagnosis (LVEF: p = 0.463; GLS: p = 0.722). In addition, a strong correlation was observed between automated and manual measurements in echocardiograms performed before diagnosis (r = 0.78 for LVEF; r = 0.83 for GLS) and at established diagnosis (r = 0.74 for LVEF; r = 0.80 for GLS).</p>
        <p>Goto et al.,<sup><xref ref-type="bibr" rid="B3">3</xref></sup> although acknowledging that ECG-based models show encouraging results, emphasize that their performance may not be sufficient for diagnosing low-prevalence diseases. The echocardiographic model developed by the authors demonstrated greater predictive accuracy compared with the ECG-based model. C-statistics ranged from 0.85-0.91 for ECG and from 0.89-1.00 for echocardiography. Moreover, in subtype analysis, the model showed superior performance in identifying ATTR amyloidosis.</p>
        <p>In a more specific population, Shiri et al.<sup><xref ref-type="bibr" rid="B4">4</xref></sup> evaluated the use of machine learning for detecting ATTR amyloidosis in patients with severe aortic stenosis. Although different diagnostic modalities are useful in the initial assessment of these patients, they are not specific for ATTR amyloidosis. Frequently, definitive diagnosis of ATTR cardiomyopathy depends on histopathological confirmation or identification of a mutation in the <italic>TTR</italic> gene associated with evidence of significant myocardial uptake on bone-seeking tracers scintigraphy. Considering the high cost of genetic testing and bone-seeking tracers scintigraphy, especially in this patient group, the authors developed a noninvasive and potentially cost-effective model based on routine clinical and echocardiographic data. Performance was satisfactory when compared with clinical, laboratory, and interventional imaging variables, with an AUC of 0.79, sensitivity of 0.80, and specificity of 0.78.</p>
        <p>Based on evidence that myocardial deformation analysis provides discriminatory value across multiple cardiac chambers, Eckstein et al.<sup><xref ref-type="bibr" rid="B7">7</xref></sup> developed a supervised model capable of differentiating cardiac amyloidosis from hypertrophic cardiomyopathy and from healthy individuals. The system showed excellent performance (AUC = 0.996; accuracy = 94%; sensitivity = 100%; F1-score = 97%), indicating that automated analysis of multichamber cardiac deformation and function may serve as a clinical decision support tool, even without the need for contrast administration.</p>
        <p>With the technological advancement of cardiovascular imaging methods, new approaches have been proposed for screening infiltrative cardiomyopathies. Barbieri et al.<sup><xref ref-type="bibr" rid="B11">11</xref></sup> developed a model based on three-dimensional transthoracic echocardiography (3D-TTE) combined with AI, aiming to differentiate various phenotypes of cardiac hypertrophy, including cardiac amyloidosis. The method proposes a reformulation of ejection fraction analysis, traditionally based on CMR, through the use of 3D-TTE integrated with an AI system. Three-dimensional acquisition allowed a more detailed and accurate analysis of LV volume, enabling a more precise calculation of ejection fraction, defined as the ratio between stroke volume and end-diastolic volume, reflecting myocardial contractile capacity. This approach provides more accurate information regarding myocardial shortening and wall thickness, key aspects in recognizing infiltrative cardiomyopathies. In conventional two-dimensional echocardiography, increased wall thickness may mask reduced myocardial shortening, resulting in an apparently preserved ejection fraction. In the context of etiological investigation of HFpEF, the model proved promising, showing higher ejection fraction in patients with hypertrophic cardiomyopathy and cardiac amyloidosis, with the latter exhibiting proportionally even higher values. Diagnostic performance was consistent, with sensitivity of 87%, specificity of 100%, and AUC of 0.959, reinforcing the potential of integrating 3D-TTE and AI in the phenotypic differentiation of myocardial hypertrophy.</p>
      </sec>
      <sec>
        <title>Artificial intelligence in positron emission tomography evaluation</title>
        <p>Similarly to other imaging modalities, PET-CT has been refined with the aim of making the diagnostic process of cardiac amyloidosis less invasive and more accurate. Deep learning-based models focused on the automated recognition of imaging patterns related to amyloid deposition stand out.</p>
        <p>Santarelli et al.<sup><xref ref-type="bibr" rid="B12">12</xref></sup> developed a model aimed at rapidly, early, and specifically identifying the presence of cardiac amyloidosis and its subtypes. The system demonstrated superior performance compared with analysis performed by a specialist with more than 10 years of experience, showing sensitivity greater than 0.8 and specificity greater than 0.89. The model was able to estimate the probability of correlation between the analyzed image and each subtype of cardiac amyloidosis. The authors also highlighted the risk of overfitting, especially in scenarios with a limited number of images available for training. In such cases, the algorithm may show high performance on training data but fail to generalize to external datasets. To mitigate this risk, strategies such as artificial data augmentation and cross-validation were employed, contributing to greater model robustness.</p>
        <p>In the study by Miller et al.,<sup><xref ref-type="bibr" rid="B13">13</xref></sup> it is recognized that visual interpretation of single-photon emission computed tomography constitutes the standard approach in the diagnostic evaluation of ATTR amyloidosis, although it is inherently subjective. The authors assessed a deep learning approach for automated volumetric quantification of technetium-99m (<sup>99m</sup>Tc)-pyrophosphate, using segmentation of anatomical structures co-registered on computed tomography attenuation maps in patients with suspected ATTR amyloidosis. The results demonstrated that deep learning-based segmentation was not influenced by the radiotracer uptake pattern and allowed automated quantification of focal uptake images, such as those obtained with <sup>99m</sup>Tc-pyrophosphate. The model showed excellent performance (AUC = 0.989; 95% CI: 0.974-1.00), indicating potential for accurate identification of patients with ATTR amyloidosis. Therefore, this approach shows potential for precise identification of patients with ATTR amyloidosis.</p>
      </sec>
      <sec>
        <title>Performance of artificial intelligence in the evaluation of bone-seeking tracers scintigraphy</title>
        <p>In the context of diagnosing cardiac amyloidosis through the application of AI to imaging analysis, it is possible to structure systems integrated into electronic health records, similar to the model described by Huda et al.,<sup><xref ref-type="bibr" rid="B8">8</xref></sup> but directed toward the automated interpretation of scintigraphy images.</p>
        <p>Delbarre et al.<sup><xref ref-type="bibr" rid="B14">14</xref></sup> proposed a deep learning model for automated analysis of whole-body <sup>99m</sup>Tc bone-seeking tracers scintigraphy, based on the premise that significant cardiac uptake on these examinations is strongly suggestive of ATTR amyloidosis. The model demonstrated sensitivity of 98.9% and specificity of 99.5% in cross-validation. In external validation, a slight reduction in sensitivity to 96.1% was observed, while specificity remained at 99.5%, with an AUC of 0.999 in both stages.</p>
        <p>For system development, cardiac uptake &#8805; 2 according to the Perugini grading scale was used as a predictive variable. The algorithm was trained using CNNs with image-level labels extracted from examinations recorded in electronic health records, enabling automated identification of patterns suggestive of cardiac amyloidosis. As also emphasized by Casta&#241;o et al.,<sup><xref ref-type="bibr" rid="B9">9</xref></sup> integration between AI and electronic record systems supports efficient screening of frequently underrecognized conditions, such as the association between increased cardiac uptake on whole-body bone-seeking tracers scintigraphy and ATTR amyloidosis, contributing to identification at earlier stages.</p>
        <p>Although bone-seeking tracers scintigraphy does not fully replace all diagnostic methods, Delbarre et al.<sup><xref ref-type="bibr" rid="B14">14</xref></sup> highlighted that when the examination is positive and there is no evidence of monoclonal gammopathy, it may allow definitive noninvasive diagnosis of ATTR cardiomyopathy, particularly in elderly or frail patients in whom myocardial biopsy carries greater risk.</p>
        <p>Considering that the diagnosis of cardiac amyloidosis can be established noninvasively through bone-seeking tracers scintigraphy and that visual assessment is inherently subjective and may result in misinterpretation, Spielvogel et al.<sup><xref ref-type="bibr" rid="B15">15</xref></sup> developed an AI system for standardized and reproducible disease screening. The model was trained using a multinational database of <sup>99m</sup>Tc-labeled bone-seeking tracers scintigraphy, encompassing different tracers and scanners. In the Austrian cohort, cross-validation demonstrated an AUC of 1.00 (95% CI: 1.00-1.00). In external validation, results remained high, with an AUC of 0.997 (95% CI: 0.993-0.999) in the United Kingdom, 0.925 (95% CI: 0.871-0.971) in China, and 1.00 (95% CI: 0.999-1.000) in the Italian cohorts. Approximately one decade ago, myocardial biopsy represented the only definitive modality for diagnosing cardiac amyloidosis. The consolidation of bone-seeking tracers scintigraphy constituted a significant advance in this scenario, particularly in the diagnosis of ATTR amyloidosis. The incorporation of AI into this modality further expands its potential by reducing interpretative subjectivity and increasing diagnostic standardization and reliability.</p>
        <p>In the aforementioned multicenter study, intense cardiac uptake was automatically and consistently identified across all tracers used in the investigation of cardiac amyloidosis. Additionally, AI-based screening for detection of uptake suggestive of cardiac amyloidosis in patients undergoing whole-body bone-seeking tracers scintigraphy represents a potentially valuable tool for early disease identification and optimization of care pathways. Implementing this strategy may support timely referral for specialized evaluation and enable earlier initiation of disease-modifying therapies, with potential impact on mortality reduction.</p>
      </sec>
      <sec>
        <title>Artificial intelligence in cardiac magnetic resonance evaluation</title>
        <p>CMR with late gadolinium enhancement (LGE) is a fundamental method in the investigation of cardiac amyloidosis, given its ability to demonstrate morphological alterations and characteristic enhancement patterns. However, its use may be limited in patients with significant renal impairment, a condition frequently associated with amyloidosis, due to the risks related to contrast administration.</p>
        <p>Ma et al.<sup><xref ref-type="bibr" rid="B16">16</xref></sup> investigated the feasibility of diagnosis using non-contrast CMR with native T1 mapping combined with automated radiomic analysis based on AI. The model was trained to recognize specific patterns of amyloid deposition and to indirectly estimate extracellular volume (ECV), a parameter traditionally calculated from pre- and post-gadolinium contrast sequences. In the proposed approach, ECV was accurately estimated through automated identification of myocardial regions of interest. The model achieved an accuracy of 86%, sensitivity of 94%, specificity of 85%, and an AUC of 0.915 in the test set. Unlike bone-seeking tracers scintigraphy, whose main applicability is concentrated on identifying ATTR amyloidosis, non-contrast CMR demonstrated potential for effective diagnosis of cardiac amyloidosis, particularly AL amyloidosis.</p>
        <p>In line with this perspective, Nowak et al.<sup><xref ref-type="bibr" rid="B17">17</xref></sup> emphasized that the diagnostic value of CMR derives from its ability to integrate multiple sequences for detailed assessment of myocardial function, edema, inflammation, and fibrosis. ECV allows noninvasive quantification of myocardial amyloid deposition and may influence therapeutic decisions.</p>
        <p>Considering that CMR is a reference modality for diagnosing cardiac amyloidosis, Agibetov et al.<sup><xref ref-type="bibr" rid="B18">18</xref></sup> observed that its findings may be nonspecific, especially in centers with lower case volumes. To minimize this risk, they developed a CNN-based algorithm applied to a cohort of 502 patients. Regardless of the deep learning technique employed, models trained with LGE images showed better performance. Fine-tuning of the model resulted in an AUC of 0.96, sensitivity of 94%, and specificity of 90%. Automated classification demonstrated performance comparable to that of human specialists. However, as this was a single-center study, generalization of the results requires caution.</p>
        <p>Martini et al.<sup><xref ref-type="bibr" rid="B19">19</xref></sup> also used deep learning for automated analysis of CMR images and estimation of the probability of cardiac amyloidosis. Among the most specific findings, they highlighted the pattern of biventricular pseudo-hypertrophy associated with diffuse transmural LGE. Automated analysis of LGE sequences in the 2C, 4C, and short-axis views was faster and showed accuracy similar to expert assessment, with an AUC of 0.982, positive predictive value of 83%, recall of 95%, and F1-score of 89%.</p>
      </sec>
      <sec>
        <title>Performance of artificial intelligence in the evaluation of genetic testing and biopsies</title>
        <p>Another promising field in the application of AI to the diagnosis of cardiac amyloidosis, especially in the AL form, involves systematizing the analysis of genetic tests aimed at identifying somatic mutations in immunoglobulin light chains. Garofalo et al.<sup><xref ref-type="bibr" rid="B20">20</xref></sup> demonstrated, through a machine learning model, an association between somatic mutations acquired during B-cell maturation and the development of cardiac amyloidosis. These mutations affect the structural stability of light chains, favoring protein misfolding and subsequent amyloid deposit formation. The proposed model achieved a sensitivity of 76%, specificity of 82%, and an AUC of 0.87, demonstrating relevant predictive capacity in identifying sequences considered toxic. In addition, the authors highlighted that reversal of these mutations may abolish the toxic phenotype, reinforcing the importance of detailed molecular characterization.</p>
        <p>Considering the diversity of pathogenic sequences involved, the use of AI represents an appropriate strategy for organizing and analyzing large volumes of genetic variables, acting as a predictor of toxicity. In this way, the algorithm may identify molecular profiles associated with higher risk of developing cardiac amyloidosis, thereby contributing to risk stratification and potential early diagnosis.</p>
        <p>In the field of histopathology, biopsy remains the definitive diagnostic evidence in amyloid cardiomyopathy, despite its invasive nature. In this context, integration between histological techniques and deep learning has also shown promise. Yang et al.<sup><xref ref-type="bibr" rid="B21">21</xref></sup> proposed a neural network-based approach capable of transforming autofluorescence images into images equivalent to those obtained by bright-field and polarized light microscopy, simulating the effect of Congo red staining.</p>
        <p>Currently, the diagnostic gold standard is based on the identification of birefringence under cross-polarized light after Congo red staining. However, this process is influenced by technical variability in staining, slide preparation quality, and availability of appropriate equipment, in addition to involving high costs. The model proposed by Yang et al.<sup><xref ref-type="bibr" rid="B21">21</xref></sup> demonstrated that digitally generated images showed quality comparable to conventionally stained slides, with potential cost reduction, lower technical dependence, and improved digital storage of samples, considering that specialized scanners for birefringence capture are not always available.</p>
        <p>Thus, although there is growing interest in noninvasive diagnostic methods for cardiac amyloidosis, advances in the application of AI to genetic and histopathological analysis also represent a relevant contribution, improving diagnostic accuracy and standardization of laboratory processes.</p>
      </sec>
      <sec>
        <title>Barriers to implementing artificial intelligence in the medical workflow</title>
        <p>The implementation of AI in medical practice has significant potential to increase diagnostic accuracy, optimize care processes, reduce costs, and support clinical decision-making. However, its incorporation into the workflow faces multifactorial challenges that can be grouped into technical, ethical, organizational, and human dimensions.</p>
        <p>From a technical perspective, AI models depend on structured, complete, and standardized datasets. However, many health care systems still operate with fragmented, inconsistent, or incomplete records, which compromises proper training and the generalizability of algorithms. In addition, historically biased data may perpetuate health care disparities, resulting in inappropriate recommendations for certain population groups. Interoperability among different information systems also represents a relevant challenge, hindering seamless integration of AI into established clinical environments.</p>
        <p>From an ethical and legal standpoint, questions arise regarding accountability in cases of clinical error involving algorithmic recommendations. Defining responsibility among developers, institutions, and professionals remains complex. This is compounded by concerns about data privacy, security, and governance, especially when there is interinstitutional data sharing for model training or validation.</p>
        <p>At the organizational level, adoption of AI-based tools requires efficient integration into care workflows. Solutions that add steps to the process or disrupt established routines tend to generate resistance and operational burden. In addition, physicians, nurses, and other professionals must be trained to critically interpret the recommendations provided by these systems, using them as support rather than as a substitute for clinical judgment. Implementation also requires investment in technological infrastructure, maintenance, and continuous model updating, which may represent a financial barrier for certain institutions.</p>
        <p>Finally, the human dimension involves aspects related to professional acceptance and patient trust. Some professionals may express distrust toward the technology or perceive AI as a threat to their clinical role. The so-called "black box" nature of algorithms, in which the decision-making process is not fully transparent, may reduce trust in the tool and hinder its incorporation into clinical practice. From the patient's perspective, trust in decisions influenced by algorithms is not yet universal. Conversely, there is a risk of excessive reliance on AI by professionals, which may compromise independent clinical reasoning if a critical and reflective stance is not maintained.</p>
      </sec>
    </sec>
    <sec sec-type="conclusions">
      <title>Conclusion</title>
      <p>Based on the findings of this review, AI emerges as a promising tool for optimizing the screening and diagnosis of cardiac amyloidosis. Its application across different diagnostic modalities demonstrates potential to accelerate disease identification, contribute to greater diagnostic accuracy, and consequently support improved clinical outcomes.</p>
      <p>The high capacity for processing and analyzing large volumes of data enables AI to recognize complex patterns, expand its ability to generalize, provided it is trained on robust and representative datasets, and assist in the early detection of cardiac amyloidosis. Furthermore, using automated models may reduce the subjectivity of human interpretation, minimize the need for invasive procedures in certain contexts, and rationalize the use of health care resources.</p>
      <p>However, despite the advances observed, the consolidation of AI in clinical practice requires continuous model refinement, external validation in diverse populations, and efficient integration into care workflows. Strategic implementation planning, training of health professionals, ethical governance in data management, and ongoing monitoring of algorithmic performance are equally essential.</p>
    </sec>
  </body>
  <back>
    <fn-group>
      <fn fn-type="financial-disclosure" id="fn1">
        <label>Sources of Funding</label>
        <p>There were no external funding sources for this study.</p>
      </fn>
      <fn fn-type="other" id="fn2">
        <label>Study Association</label>
        <p>This study is not associated with any thesis or dissertation work.</p>
      </fn>
      <fn fn-type="other" id="fn3">
        <label>Ethics Approval and Consent to Participate</label>
        <p>This article does not contain any studies with human participants or animals performed by any of the authors.</p>
      </fn>
      <fn fn-type="other" id="fn4">
        <label>Use of Artificial Intelligence</label>
        <p>The authors did not use any artificial intelligence tools in the development of this work.</p>
      </fn>
    </fn-group>
    <sec sec-type="data-availability" specific-use="data-in-article">
      <title>Availability of Research Data</title>
      <p>The underlying content of the research text is contained within the manuscript.</p>
    </sec>
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  <sub-article article-type="translation" id="S1" xml:lang="pt">
    <front-stub>
      <article-id pub-id-type="doi">10.36660/abcimg.20260016</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigo de Revis&#227;o</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>O Uso da Intelig&#234;ncia Artificial no Diagn&#243;stico da Amiloidose Card&#237;aca: Revis&#227;o Integrativa</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-2331-6871</contrib-id>
          <name>
            <surname>Lemos</surname>
            <given-names>Nilson Batista</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">
            <sup>1</sup>
          </xref>
          <xref ref-type="corresp" rid="c2"/>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>an&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <role>reda&#231;&#227;o do manuscrito e revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do intelectual importante</role>
          <role>obten&#231;&#227;o de dados</role>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0009-0006-1640-0975</contrib-id>
          <name>
            <surname>Ara&#250;jo</surname>
            <given-names>Gabriela Aparecida Moreira</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">
            <sup>1</sup>
          </xref>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>an&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <role>reda&#231;&#227;o do manuscrito e revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do intelectual importante</role>
          <role>obten&#231;&#227;o de dados</role>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0001-8809-8783</contrib-id>
          <name>
            <surname>Melo</surname>
            <given-names>Marcelo Dantas Tavares de</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">
            <sup>1</sup>
          </xref>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>an&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <role>reda&#231;&#227;o do manuscrito e revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do intelectual importante</role>
        </contrib>
        <aff id="aff2">
          <label>1</label>
          <addr-line>
            <named-content content-type="city">Jo&#227;o Pessoa</named-content>
            <named-content content-type="state">PB</named-content>
          </addr-line>
          <country country="BR">Brasil</country>
          <institution content-type="original">Universidade Federal da Para&#237;ba, Jo&#227;o Pessoa, PB &#8211; Brasil</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c2"><label>Correspond&#234;ncia:</label><bold>Nilson Batista Lemos</bold> &#8226; Universidade Federal da Para&#237;ba. Campus I Lot., Cidade Universitaria. CEP: <postal-code>58051-900</postal-code>. Jo&#227;o Pessoa, PB &#8211; Brasil E-mail: <email>nilsonlemos18@gmail.com</email> </corresp>
        <fn fn-type="coi-statement">
          <label>Potencial Conflito de Interesse</label>
          <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
        </fn>
        <fn fn-type="edited-by">
          <label>Editor respons&#225;vel pela revis&#227;o:</label>
          <p>Marcelo Tavares</p>
        </fn>
      </author-notes>
      <abstract>
        <title>Resumo</title>
        <sec>
          <title>Fundamento:</title>
          <p>A amiloidose card&#237;aca &#233; uma forma rara de cardiomiopatia infiltrativa caracterizada pela deposi&#231;&#227;o de prote&#237;nas no mioc&#225;rdio, resultando em aumento da espessura parietal, comprometimento da fun&#231;&#227;o ventricular e poss&#237;vel progress&#227;o para insufici&#234;ncia card&#237;aca. O diagn&#243;stico &#233; desafiador devido &#224; baixa preval&#234;ncia da doen&#231;a e &#224; inespecificidade das manifesta&#231;&#245;es cl&#237;nicas. Nesse cen&#225;rio, a aplica&#231;&#227;o da intelig&#234;ncia artificial (IA) &#224; an&#225;lise de exames m&#233;dicos surge como estrat&#233;gia promissora para detec&#231;&#227;o precoce, diagn&#243;stico mais preciso e in&#237;cio oportuno do tratamento.</p>
        </sec>
        <sec>
          <title>M&#233;todos:</title>
          <p>Realizou-se revis&#227;o integrativa da literatura sobre o uso da IA no diagn&#243;stico da amiloidose card&#237;aca. Foram pesquisados artigos publicados entre 2019 e 2024 nas bases de dados PubMed, Scopus, Web of Science, Embase e Cochrane Library.</p>
        </sec>
        <sec>
          <title>Resultados:</title>
          <p>Dos 420 artigos inicialmente identificados, 21 atenderam aos crit&#233;rios de elegibilidade e foram inclu&#237;dos na an&#225;lise final. Observou-se predom&#237;nio de estudos observacionais retrospectivos com aplica&#231;&#227;o de modelos de aprendizado de m&#225;quina. Entre as modalidades diagn&#243;sticas avaliadas em associa&#231;&#227;o com IA, o eletrocardiograma e o ecocardiograma foram os exames mais frequentemente estudados.</p>
        </sec>
        <sec>
          <title>Conclus&#227;o:</title>
          <p>A IA demonstra elevado potencial para aprimorar o rastreio e o diagn&#243;stico da amiloidose card&#237;aca quando aplicada &#224; an&#225;lise de exames cl&#237;nicos e de imagem. Os achados desta revis&#227;o indicam que a IA pode acelerar o processo diagn&#243;stico, reduzir a necessidade de procedimentos invasivos e otimizar o uso de recursos em sa&#250;de. Entretanto, para ampliar sua integra&#231;&#227;o &#224; pr&#225;tica cl&#237;nica e sua capacidade de generaliza&#231;&#227;o, s&#227;o necess&#225;rios aprimoramentos adicionais nos modelos e valida&#231;&#245;es em popula&#231;&#245;es mais diversas.</p>
        </sec>
      </abstract>
      <kwd-group xml:lang="pt">
        <title>Palavras-chave:</title>
        <kwd>Amiloidose</kwd>
        <kwd>Intelig&#234;ncia Artificial</kwd>
        <kwd>Diagn&#243;stico</kwd>
      </kwd-group>
      <funding-group>
        <funding-statement><bold>Fontes de Financiamento</bold>: O presente estudo n&#227;o teve fontes de financiamento externas.</funding-statement>
      </funding-group>
    </front-stub>
    <body>
      <fig id="f3">
        <graphic xlink:href="2675-312X-abcic-39-01-e20260016-0016i-gf01-pt.tif"/></fig>
      <sec sec-type="intro">
        <title>Introdu&#231;&#227;o</title>
        <p>A amiloidose &#233; um termo gen&#233;rico utilizado para descrever a deposi&#231;&#227;o extracelular de fibrilas formadas por subunidades proteicas de baixo peso molecular, derivadas de diferentes prote&#237;nas precursoras. Os dep&#243;sitos amiloides podem resultar em ampla variedade de manifesta&#231;&#245;es cl&#237;nicas, que variam conforme o tipo de prote&#237;na envolvida, a quantidade depositada e a localiza&#231;&#227;o tecidual. Na g&#234;nese desses dep&#243;sitos, pept&#237;deos inicialmente sol&#250;veis sofrem altera&#231;&#245;es conformacionais, adquirindo predominantemente uma estrutura de folha beta-pregueada antiparalela, o que favorece seu empilhamento em fibrilas torcidas.<sup><xref ref-type="bibr" rid="B1">1</xref></sup></p>
        <p>Existem dezenas de formas sist&#234;micas e localizadas de amiloidose. Entre elas, quatro prote&#237;nas precursoras podem originar dep&#243;sitos tanto localizados quanto sist&#234;micos. As principais formas sist&#234;micas s&#227;o a amiloidose de cadeia leve de imunoglobulina (AL, em ingl&#234;s) e a amiloidose por transtirretina (ATTR, em ingl&#234;s). Essas formas s&#227;o nomeadas de acordo com a prote&#237;na precursora do dep&#243;sito amiloide (AL ou ATTR) e s&#227;o respons&#225;veis por aproximadamente 95% dos casos de amiloidose card&#237;aca. As demais formas correspondem a outros subtipos de amiloidose, igualmente relevantes do ponto de vista cl&#237;nico.<sup><xref ref-type="bibr" rid="B2">2</xref>,<xref ref-type="bibr" rid="B3">3</xref></sup></p>
        <p>A amiloidose por ATTR caracteriza-se pelo dobramento incorreto e subsequente deposi&#231;&#227;o da transtirretina, prote&#237;na respons&#225;vel pelo transporte do horm&#244;nio tireoidiano e da vitamina A. Pode apresentar-se na forma selvagem ou heredit&#225;ria.<sup><xref ref-type="bibr" rid="B2">2</xref>-<xref ref-type="bibr" rid="B4">4</xref></sup> Similarmente, a amiloidose AL decorre do ac&#250;mulo de cadeias leves de imunoglobulinas mal dobradas, produzidas por c&#233;lulas plasm&#225;ticas associadas a discrasias.<sup><xref ref-type="bibr" rid="B2">2</xref>,<xref ref-type="bibr" rid="B3">3</xref></sup></p>
        <p>No contexto da amiloidose card&#237;aca, trata-se de uma forma rara de cardiomiopatia progressiva, cuja preval&#234;ncia populacional ainda n&#227;o est&#225; bem estabelecida.<sup><xref ref-type="bibr" rid="B5">5</xref></sup> A doen&#231;a &#233; causada pela deposi&#231;&#227;o mioc&#225;rdica de prote&#237;nas amiloides mal dobradas, resultando em cardiomiopatia restritiva, com poss&#237;vel progress&#227;o para insufici&#234;ncia card&#237;aca, dist&#250;rbios do sistema de condu&#231;&#227;o e morte card&#237;aca.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B6">6</xref></sup> Pode manifestar-se com sinais e sintomas cardiovasculares ou ser diagnosticada durante a investiga&#231;&#227;o de manifesta&#231;&#245;es extracard&#237;acas da doen&#231;a.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B6">6</xref>,<xref ref-type="bibr" rid="B7">7</xref></sup> Devido ao fen&#243;tipo cl&#237;nico heterog&#234;neo e &#224;s manifesta&#231;&#245;es frequentemente inespec&#237;ficas, o diagn&#243;stico e o manejo tendem a ocorrer de forma tardia.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B6">6</xref></sup></p>
        <p>No que se refere &#224; abordagem diagn&#243;stica da amiloidose card&#237;aca, &#233; fundamental reconhecer cen&#225;rios cl&#237;nicos e altera&#231;&#245;es em exames complementares que indiquem a necessidade de investiga&#231;&#227;o. Entretanto, o diagn&#243;stico &#233; desafiador, especialmente por se tratar de doen&#231;a frequentemente indolente, cujos sintomas podem se sobrepor aos de cardiopatias mais prevalentes.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B5">5</xref></sup> Dependendo do contexto cl&#237;nico e da disponibilidade de recursos, diversas ferramentas podem ser empregadas, incluindo eletrocardiograma (ECG), ecocardiograma, resson&#226;ncia magn&#233;tica card&#237;aca (RMC), cintilografia com tra&#231;adores &#243;sseos, pesquisa de prote&#237;na monoclonal por imunofixa&#231;&#227;o e bi&#243;psia do tecido acometido. Cada m&#233;todo apresenta caracter&#237;sticas pr&#243;prias e diferentes n&#237;veis de acur&#225;cia diagn&#243;stica (<xref ref-type="fig" rid="f3">Figura Central</xref>).</p>
        <p>Alguns achados podem aumentar a suspeita cl&#237;nica de amiloidose card&#237;aca, como a discord&#226;ncia entre o aumento da espessura da parede do ventr&#237;culo esquerdo (VE) e a baixa voltagem do QRS, hipertrofia inexplicada do VE, estenose a&#243;rtica de baixo fluxo e baixo gradiente, preserva&#231;&#227;o apical relativa da deforma&#231;&#227;o longitudinal, padr&#227;o de realce tardio subendoc&#225;rdico difuso e circunferencial do VE na RMC e avidez mioc&#225;rdica por tra&#231;adores &#243;sseos na cintilografia com tra&#231;adores &#243;sseos.</p>
        <p>Apesar da diversidade de m&#233;todos diagn&#243;sticos dispon&#237;veis, a amiloidose card&#237;aca permanece subdiagnosticada,<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B5">5</xref>-<xref ref-type="bibr" rid="B7">7</xref></sup> o que implica importantes repercuss&#245;es na qualidade de vida dos pacientes. Paralelamente, o desenvolvimento de terapias capazes de melhorar desfechos cl&#237;nicos tem impulsionado a busca por estrat&#233;gias que ampliem a taxa de diagn&#243;stico. Essas interven&#231;&#245;es podem reduzir ou estabilizar a deposi&#231;&#227;o proteica, com consequente diminui&#231;&#227;o do risco relativo de hospitaliza&#231;&#245;es, da morbidade e da mortalidade associadas &#224; doen&#231;a.</p>
        <p>Diante da necessidade de detec&#231;&#227;o precoce da amiloidose card&#237;aca, torna-se essencial o desenvolvimento de mecanismos que otimizem o rastreio e o diagn&#243;stico, com menores custos e riscos.<sup><xref ref-type="bibr" rid="B3">3</xref></sup> Nesse contexto, esta revis&#227;o tem como objetivo apresentar os principais avan&#231;os na detec&#231;&#227;o da doen&#231;a, com &#234;nfase em ferramentas tecnol&#243;gicas promissoras no &#226;mbito da medicina diagn&#243;stica, especialmente a intelig&#234;ncia artificial (IA).</p>
        <p>A IA constitui um ramo da ci&#234;ncia da computa&#231;&#227;o dedicado ao desenvolvimento de sistemas capazes de executar tarefas que simulam fun&#231;&#245;es cognitivas humanas, como tomada de decis&#227;o e racioc&#237;nio complexo. No campo do diagn&#243;stico m&#233;dico, esses sistemas s&#227;o treinados por meio de t&#233;cnicas de aprendizado de m&#225;quina, nas quais grandes volumes de dados, frequentemente imagens, s&#227;o utilizados para o reconhecimento de padr&#245;es. Entre as abordagens mais empregadas destacam-se as redes neurais convolucionais (CNNs, na sigla em ingl&#234;s), compostas por m&#250;ltiplas camadas que extraem caracter&#237;sticas progressivamente mais complexas dos dados analisados, permitindo a identifica&#231;&#227;o automatizada de padr&#245;es em imagens e outros tipos de informa&#231;&#227;o. De modo geral, quanto maior e mais representativo o conjunto de dados utilizado no treinamento, maior tende a ser a precis&#227;o do modelo.</p>
        <p>A incorpora&#231;&#227;o da IA &#224; pr&#225;tica m&#233;dica possibilita aprimorar o rastreio de doen&#231;as raras e aumentar a acur&#225;cia diagn&#243;stica. Nesse cen&#225;rio, a IA mostra-se particularmente promissora para doen&#231;as raras, frequentemente pouco reconhecidas na pr&#225;tica cl&#237;nica. Sistemas automatizados podem integrar m&#250;ltiplos sinais, sintomas e achados complementares, contribuindo para direcionar o racioc&#237;nio cl&#237;nico. Assim, habilidades centrais na medicina, como o reconhecimento de padr&#245;es, v&#234;m sendo incorporadas a modelos computacionais com o objetivo de ampliar a confiabilidade diagn&#243;stica e apoiar a tomada de decis&#227;o no cotidiano m&#233;dico.</p>
        <p>Diversos estudos t&#234;m investigado a aplicabilidade da IA no diagn&#243;stico precoce da amiloidose card&#237;aca. Entre as abordagens mais recentes destacam-se a integra&#231;&#227;o da IA a m&#233;todos de imagem, como tomografia por emiss&#227;o de f&#243;ton &#250;nico (SPECT), cintilografia com tra&#231;adores &#243;sseos e RMC, bem como sua aplica&#231;&#227;o na an&#225;lise automatizada de ECGs, dados gen&#233;ticos e perfis fenot&#237;picos de altera&#231;&#245;es card&#237;acas. Esses aspectos ser&#227;o discutidos ao longo desta revis&#227;o.</p>
      </sec>
      <sec sec-type="methods">
        <title>M&#233;todos</title>
        <p>O presente estudo caracteriza-se como uma revis&#227;o integrativa de literatura, com o objetivo de analisar criticamente o uso da IA no diagn&#243;stico da amiloidose card&#237;aca. A condu&#231;&#227;o da revis&#227;o seguiu seis etapas metodol&#243;gicas: i) defini&#231;&#227;o da pergunta de pesquisa; ii) estabelecimento dos crit&#233;rios de inclus&#227;o e sele&#231;&#227;o da amostra; iii) identifica&#231;&#227;o dos estudos pr&#233;-selecionados e selecionados; iv) organiza&#231;&#227;o e representa&#231;&#227;o dos estudos inclu&#237;dos; v) an&#225;lise cr&#237;tica dos dados; e vi) s&#237;ntese do conhecimento dispon&#237;vel.</p>
        <p>As buscas foram realizadas nas bases de dados PubMed, Scopus, Web of Science, Embase e Cochrane Library. A estrat&#233;gia de busca foi elaborada a partir dos descritores "artificial intelligence", "amyloidosis" e "diagnosis", presentes no <italic>Medical Subject Headings</italic> e no <italic>Embase Subject Headings</italic>, combinados por meio do operador booleano AND.</p>
        <p>Foram inclu&#237;dos estudos originais e metan&#225;lises publicados entre 2019 e 2024 que avaliaram a aplica&#231;&#227;o da IA no diagn&#243;stico da amiloidose card&#237;aca. Foram exclu&#237;dos artigos que n&#227;o atenderam aos crit&#233;rios de inclus&#227;o, bem como revis&#245;es narrativas, relatos de caso, editoriais e estudos com metodologia considerada inadequada.</p>
        <p>Ap&#243;s a sele&#231;&#227;o dos artigos, procedeu-se &#224; avalia&#231;&#227;o da qualidade metodol&#243;gica, com o objetivo de assegurar maior rigor na interpreta&#231;&#227;o dos achados e robustez &#224;s conclus&#245;es. Para essa etapa, utilizou-se a ferramenta de avalia&#231;&#227;o cr&#237;tica do JBI, que contempla crit&#233;rios espec&#237;ficos conforme o delineamento do estudo, incluindo aspectos relacionados &#224; amostra, metodologia, an&#225;lise de dados, controle de vieses e considera&#231;&#245;es &#233;ticas. A classifica&#231;&#227;o da qualidade baseia-se na propor&#231;&#227;o de respostas afirmativas aos crit&#233;rios avaliados, permitindo a compara&#231;&#227;o entre estudos e a an&#225;lise cr&#237;tica de seus resultados.</p>
      </sec>
      <sec sec-type="results">
        <title>Resultados</title>
        <p>A estrat&#233;gia de busca resultou em 420 artigos, distribu&#237;dos da seguinte forma: 124 identificados no PubMed, 61 na Web of Science, 84 no Scopus, 147 no Embase e 4 na Cochrane Library. Ap&#243;s a remo&#231;&#227;o de 192 estudos duplicados, permaneceram 228 artigos para triagem.</p>
        <p>A leitura de t&#237;tulos e resumos resultou na sele&#231;&#227;o de 43 estudos para avalia&#231;&#227;o na &#237;ntegra. Ap&#243;s a aplica&#231;&#227;o dos crit&#233;rios de elegibilidade, 21 artigos foram inclu&#237;dos na an&#225;lise final (<xref ref-type="fig" rid="f4">Figura 1</xref>).</p>
        <fig id="f4">
          <label>Figura 1</label>
          <caption>
            <title>Fluxograma do processo de sele&#231;&#227;o dos estudos inclu&#237;dos na revis&#227;o integrativa.</title>
          </caption>
          <graphic xlink:href="2675-312X-abcic-39-01-e20260016-0016i-gf02-pt.tif"/></fig>
        <p>Quanto &#224; avalia&#231;&#227;o metodol&#243;gica, segundo os crit&#233;rios do JBI, a maioria dos estudos foi classificada com qualidade metodol&#243;gica entre boa e excelente, com pontua&#231;&#227;o variando de 6 a 8 pontos. Entre os principais fatores que contribu&#237;ram para essa classifica&#231;&#227;o destacam-se o emprego de m&#233;tricas estat&#237;sticas robustas e a utiliza&#231;&#227;o de valida&#231;&#227;o cruzada nos modelos de IA desenvolvidos.</p>
        <p>Como limita&#231;&#245;es, observou-se a aus&#234;ncia de confirma&#231;&#227;o diagn&#243;stica por padr&#227;o-ouro da amiloidose card&#237;aca em parte dos estudos, bem como a escassez de valida&#231;&#227;o externa dos modelos propostos, o que limita a generaliza&#231;&#227;o dos achados. Os resultados detalhados da avalia&#231;&#227;o metodol&#243;gica est&#227;o apresentados na <xref ref-type="table" rid="t2">Tabela 1</xref>.</p>
        <table-wrap id="t2">
          <label>Tabela 1</label>
          <caption>
            <title>Caracter&#237;sticas metodol&#243;gicas e avalia&#231;&#227;o da qualidade dos estudos inclu&#237;dos</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup width="20%">
              <col/>
              <col/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead style="border-top: thin solid; border-bottom: thin solid; border-color: #000000">
              <tr style="background-color:#C58874">
                <th align="left" valign="middle">N&#186;</th>
                <th align="center" valign="middle">Estudo (autor/ano)</th>
                <th align="center" valign="middle">Delineamento</th>
                <th align="center" valign="middle">Pontua&#231;&#227;o (JBI/8)</th>
                <th align="center" valign="middle">Avalia&#231;&#227;o metodol&#243;gica</th>
              </tr>
            </thead>
            <tbody style="border-bottom: thin solid; border-color: #000000">
              <tr>
                <td align="left" valign="middle">1</td>
                <td align="center" valign="middle">Agibetov et al. (2021)<sup><xref ref-type="bibr" rid="B18">18</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com resson&#226;ncia magn&#233;tica card&#237;aca e aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">2</td>
                <td align="center" valign="middle">Barbieri et al. (2024)<sup><xref ref-type="bibr" rid="B11">11</xref></sup></td>
                <td align="center" valign="middle">Estudo com ecocardiograma transtor&#225;cico tridimensional automatizado associado a aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr>
                <td align="left" valign="middle">3</td>
                <td align="center" valign="middle">Casta&#241;o et al. (2024)<sup><xref ref-type="bibr" rid="B9">9</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo caso-controle com aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">4</td>
                <td align="center" valign="middle">Cotella et al. (2023)<sup><xref ref-type="bibr" rid="B2">2</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com ecocardiograma e aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr>
                <td align="left" valign="middle">5</td>
                <td align="center" valign="middle">Delbarre et al. (2023)<sup><xref ref-type="bibr" rid="B14">14</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo multic&#234;ntrico com cintilografia com tra&#231;adores &#243;sseos analisada por aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">8</td>
                <td align="center" valign="middle">Excelente</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">6</td>
                <td align="center" valign="middle">Eckstein et al. (2022)<sup><xref ref-type="bibr" rid="B7">7</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional de coorte com ecocardiograma e uso de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">6</td>
                <td align="center" valign="middle">Boa qualidade</td>
              </tr>
              <tr>
                <td align="left" valign="middle">7</td>
                <td align="center" valign="middle">Garofalo et al. (2021)<sup><xref ref-type="bibr" rid="B20">20</xref></sup></td>
                <td align="center" valign="middle">Estudo computacional preditivo com valida&#231;&#227;o experimental focado em avalia&#231;&#227;o gen&#233;tica por aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">6</td>
                <td align="center" valign="middle">Boa qualidade</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">8</td>
                <td align="center" valign="middle">Goto et al. (2021)<sup><xref ref-type="bibr" rid="B3">3</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional multic&#234;ntrico com uso de eletrocardiograma e ecocardiograma</td>
                <td align="center" valign="middle">8</td>
                <td align="center" valign="middle">Excelente</td>
              </tr>
              <tr>
                <td align="left" valign="middle">9</td>
                <td align="center" valign="middle">Harmon et al. (2023)<sup><xref ref-type="bibr" rid="B10">10</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com eletrocardiograma e aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">10</td>
                <td align="center" valign="middle">Huda et al. (2021)<sup><xref ref-type="bibr" rid="B8">8</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr>
                <td align="left" valign="middle">11</td>
                <td align="center" valign="middle">Ma et al. (2024)<sup><xref ref-type="bibr" rid="B16">16</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com resson&#226;ncia magn&#233;tica card&#237;aca sem contraste e uso de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">12</td>
                <td align="center" valign="middle">Martini et al. (2020)<sup><xref ref-type="bibr" rid="B19">19</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional prospectivo com resson&#226;ncia magn&#233;tica card&#237;aca e aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">8</td>
                <td align="center" valign="middle">Excelente</td>
              </tr>
              <tr>
                <td align="left" valign="middle">13</td>
                <td align="center" valign="middle">Miller et al. (2024)<sup><xref ref-type="bibr" rid="B13">13</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com tomografia por emiss&#227;o de p&#243;sitrons e segmenta&#231;&#227;o automatizada</td>
                <td align="center" valign="middle">8</td>
                <td align="center" valign="middle">Excelente</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">14</td>
                <td align="center" valign="middle">Nowak et al. (2024)<sup><xref ref-type="bibr" rid="B17">17</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com resson&#226;ncia magn&#233;tica card&#237;aca, mapeamento T1 e uso de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr>
                <td align="left" valign="middle">15</td>
                <td align="center" valign="middle">Santarelli et al. (2021)<sup><xref ref-type="bibr" rid="B12">12</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional prospectivo com tomografia por emiss&#227;o de p&#243;sitrons e aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">16</td>
                <td align="center" valign="middle">Schrutka et al. (2022)<sup><xref ref-type="bibr" rid="B6">6</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional prospectivo caso-controle com aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">6</td>
                <td align="center" valign="middle">Boa qualidade</td>
              </tr>
              <tr>
                <td align="left" valign="middle">17</td>
                <td align="center" valign="middle">Shiri et al. (2025)<sup><xref ref-type="bibr" rid="B4">4</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional prospectivo de coorte &#250;nica com aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">18</td>
                <td align="center" valign="middle">Spielvogel et al. (2024)<sup><xref ref-type="bibr" rid="B15">15</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo multic&#234;ntrico com cintilografia com tra&#231;adores &#243;sseos e uso de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">8</td>
                <td align="center" valign="middle">Excelente</td>
              </tr>
              <tr>
                <td align="left" valign="middle">19</td>
                <td align="center" valign="middle">Vrudhula et al. (2024)<sup><xref ref-type="bibr" rid="B5">5</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">6</td>
                <td align="center" valign="middle">Boa qualidade</td>
              </tr>
              <tr style="background-color:#E8CCBF">
                <td align="left" valign="middle">20</td>
                <td align="center" valign="middle">Yang et al. (2024)<sup><xref ref-type="bibr" rid="B21">21</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional com an&#225;lise histopatol&#243;gica digital utilizando rede neural e autofluoresc&#234;ncia</td>
                <td align="center" valign="middle">7</td>
                <td align="center" valign="middle">Alta qualidade</td>
              </tr>
              <tr>
                <td align="left" valign="middle">21</td>
                <td align="center" valign="middle">Zhang et al. (2023)<sup><xref ref-type="bibr" rid="B1">1</xref></sup></td>
                <td align="center" valign="middle">Estudo observacional retrospectivo com ecocardiograma e aplica&#231;&#227;o de aprendizado de m&#225;quina</td>
                <td align="center" valign="middle">6</td>
                <td align="center" valign="middle">Boa qualidade</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
      <sec sec-type="discussion">
        <title>Discuss&#227;o</title>
        <p>O uso da IA como ferramenta de apoio ao diagn&#243;stico de doen&#231;as raras, como a amiloidose card&#237;aca, tem sido considerado promissor, especialmente no contexto de patologias com elevada heterogeneidade cl&#237;nica e frequentemente sub-reconhecidas por m&#233;dicos generalistas. A identifica&#231;&#227;o precoce da doen&#231;a pode modificar sua hist&#243;ria natural e melhorar o progn&#243;stico. Nesse cen&#225;rio, esta revis&#227;o buscou enfatizar o potencial das ferramentas diagn&#243;sticas j&#225; consolidadas para a avalia&#231;&#227;o da amiloidose card&#237;aca quando associadas a sistemas baseados em aprendizado de m&#225;quina, abordagem contemplada por todos os estudos inclu&#237;dos.</p>
        <p>Com o objetivo de organizar a an&#225;lise dos achados, o desempenho da IA ser&#225; discutido de acordo com as diferentes modalidades diagn&#243;sticas empregadas no rastreio e na avalia&#231;&#227;o da amiloidose card&#237;aca.</p>
        <sec>
          <title>Desempenho da intelig&#234;ncia artificial na avalia&#231;&#227;o de dados de prontu&#225;rios e exames laboratoriais</title>
          <p>Entre as estrat&#233;gias de rastreio da cardiopatia amiloide, destaca-se a utiliza&#231;&#227;o de dados extra&#237;dos de prontu&#225;rios eletr&#244;nicos de pacientes com insufici&#234;ncia card&#237;aca (IC) com fra&#231;&#227;o de eje&#231;&#227;o preservada (ICFEp). Com o objetivo de diferenciar etiologia amiloide, especialmente do amiloidose por ATTR do tipo selvagem (ATTRwt), de etiologia n&#227;o amiloide, Huda et al.<sup><xref ref-type="bibr" rid="B8">8</xref></sup> coletou dados de prontu&#225;rio eletr&#244;nico e desenvolveu uma IA capaz de realizar a triagem e identifica&#231;&#227;o de pacientes com amiloidose por ATTRwt. O sistema apresentou &#225;rea sob a curva (AUC, em ingl&#234;s) caracter&#237;stica de opera&#231;&#227;o do receptor de 0,80. O desempenho foi sustentado pela identifica&#231;&#227;o de comorbidades mais prevalentes no grupo com etiologia amiloide, como fibrila&#231;&#227;o atrial e doen&#231;a renal cr&#244;nica, e no grupo n&#227;o amiloide, como hipertens&#227;o arterial sist&#234;mica, diabetes melito, obesidade e doen&#231;a arterial coronariana, utilizadas como vari&#225;veis preditoras.</p>
          <p>Posteriormente, Casta&#241;o et al.<sup><xref ref-type="bibr" rid="B9">9</xref></sup> aprimoraram o modelo ao direcionar a an&#225;lise para 11 fen&#243;tipos principais associados &#224; amiloidose card&#237;aca, incluindo s&#237;ndrome do t&#250;nel do carpo e arritmias. O modelo apresentou precis&#227;o (74%), sensibilidade (77%) e especificidade (72%), com AUC de 0,82. Embora tenha havido discreta redu&#231;&#227;o em alguns par&#226;metros de desempenho, o modelo foi simplificado em termos de programa&#231;&#227;o, favorecendo sua implementa&#231;&#227;o em ambientes hospitalares e ampliando o potencial de rastreio populacional.</p>
          <p>Os estudos de Huda et al.<sup><xref ref-type="bibr" rid="B8">8</xref></sup> e Casta&#241;o et al.<sup><xref ref-type="bibr" rid="B9">9</xref></sup> demonstram a viabilidade de triagem automatizada por meio da extra&#231;&#227;o sistematizada de dados cl&#237;nicos, processo que seria oneroso e operacionalmente complexo se realizado manualmente. Embora tais modelos estejam limitados &#224; qualidade dos registros codificados pela Classifica&#231;&#227;o Internacional de Doen&#231;as e aos fen&#243;tipos documentados, sem integra&#231;&#227;o direta de exames laboratoriais ou de imagem para tipifica&#231;&#227;o definitiva, configuram ferramentas relevantes para rastreio em larga escala, direcionando pacientes com maior probabilidade para investiga&#231;&#227;o complementar.</p>
          <p>Adicionalmente, fen&#243;tipos reconhecidos pelo modelo, como s&#237;ndrome do t&#250;nel do carpo, podem preceder o desenvolvimento de IC, o que sugere potencial aplica&#231;&#227;o da IA em est&#225;gios pr&#233;-cl&#237;nicos, com implica&#231;&#245;es na identifica&#231;&#227;o precoce da amiloidose por ATTR.</p>
        </sec>
        <sec>
          <title>Desempenho da intelig&#234;ncia artificial na avalia&#231;&#227;o eletrocardiogr&#225;fica</title>
          <p>A aplica&#231;&#227;o da IA na an&#225;lise de ECGs tem se destacado como estrat&#233;gia de triagem, considerando que se trata de exame amplamente dispon&#237;vel, de baixo custo e n&#227;o invasivo.<sup><xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B5">5</xref></sup> A etapa de valida&#231;&#227;o dos modelos constitui fase fundamental no desenvolvimento dessas ferramentas, pois envolve o teste de m&#250;ltiplas vari&#225;veis em diferentes popula&#231;&#245;es.<sup><xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B6">6</xref></sup></p>
          <p>Harmon et al.<sup><xref ref-type="bibr" rid="B10">10</xref></sup> desenvolveram um algoritmo aplic&#225;vel a popula&#231;&#245;es diversas, incluindo diferentes ra&#231;as e sexos. O modelo apresentou AUC de 0,84 (intervalo de confian&#231;a [IC] de 95%: 0,82-0,86), mantendo desempenho consistente entre subgrupos, com exce&#231;&#227;o da popula&#231;&#227;o hisp&#226;nica, possivelmente sub-representada na amostra. O algoritmo apresentou melhor desempenho em ECGs com baixa voltagem e padr&#245;es compat&#237;veis com infarto pr&#233;vio, e menor desempenho em bloqueio de ramo esquerdo e hipertrofia do VE. Esses achados sugerem necessidade de maior diversidade amostral, sem invalidar o uso da ferramenta como m&#233;todo de triagem.</p>
          <p>Vrudhula et al.<sup><xref ref-type="bibr" rid="B5">5</xref></sup> avaliaram aproximadamente 1,3 milh&#227;o de ECGs provenientes de 341.989 pacientes. Os diferentes modelos testados apresentaram AUC variando de 0,660 (IC 95%: 0,642-0,736) a 0,898 (IC 95%: 0,868-0,924), demonstrando potencial relevante para rastreio e indica&#231;&#227;o de investiga&#231;&#227;o complementar. Entretanto, ressalta-se que, diante da raridade e do subdiagn&#243;stico da amiloidose card&#237;aca, os modelos frequentemente s&#227;o treinados com n&#250;mero limitado de casos confirmados.</p>
          <p>De forma semelhante, Goto et al.<sup><xref ref-type="bibr" rid="B3">3</xref></sup> relataram desempenho expressivo, com estat&#237;stica C de 0,91 (IC 95%: 0,90-0,93) no conjunto de teste do Brigham and Women's Hospital, 0,85 (0,82-0,87) no Massachusetts General Hospital e 0,86 (0,83-0,88) na University of California, San Francisco. Contudo, os autores enfatizam que caracter&#237;sticas isoladas do ECG n&#227;o apresentam sensibilidade ou especificidade suficientes para uso como heur&#237;sticas independentes, sendo recomendada sua integra&#231;&#227;o com outras vari&#225;veis cl&#237;nicas e diagn&#243;sticas para otimiza&#231;&#227;o do modelo.</p>
          <p>Schrutka et al.<sup><xref ref-type="bibr" rid="B6">6</xref></sup> tamb&#233;m refor&#231;am que o modelo proposto pode auxiliar na suspei&#231;&#227;o de amiloidose card&#237;aca mesmo na aus&#234;ncia de m&#233;todos avan&#231;ados de imagem. No referido estudo, foram avaliados 20 pacientes com amiloidose card&#237;aca por transtirretina, 11 com ICFEp, 30 com amiloidose card&#237;aca e 50 com outras etiologias de IC. A presen&#231;a de padr&#227;o de ECG de baixa voltagem associada ao aumento da espessura da parede do VE foi altamente sugestiva de amiloidose card&#237;aca, o que permitiu sua diferencia&#231;&#227;o em rela&#231;&#227;o &#224; cardiomiopatia hipertensiva ou hipertr&#243;fica. Na an&#225;lise dos padr&#245;es de ECG, observou-se que o padr&#227;o 1 esteve presente em 78% dos pacientes com amiloidose por AL e em 58% daqueles com amiloidose por ATTR (p = 0,009), enquanto o padr&#227;o 2 foi identificado em 7% dos casos de amiloidose por AL e em 23% dos casos de amiloidose por ATTR (p = 0,006). A aus&#234;ncia de padr&#227;o espec&#237;fico foi observada em 16% dos pacientes com amiloidose por AL e em 18% dos pacientes com amiloidose por ATTR (p = 0,620).</p>
        </sec>
        <sec>
          <title>Desempenho da intelig&#234;ncia artificial na avalia&#231;&#227;o ecocardiogr&#225;fica</title>
          <p>Considerando a versatilidade da ecocardiografia e seu papel central na investiga&#231;&#227;o diagn&#243;stica da amiloidose card&#237;aca, o desenvolvimento de modelos de IA capazes de reduzir a variabilidade operacional e aprimorar a acur&#225;cia diagn&#243;stica mostra-se relevante.</p>
          <p>Xiaofeng Zhang et al.<sup><xref ref-type="bibr" rid="B1">1</xref></sup> observaram que ainda existem poucos estudos sobre an&#225;lise de textura mioc&#225;rdica baseada em ecocardiografia e que a avalia&#231;&#227;o visual humana apresenta limita&#231;&#245;es para caracteriza&#231;&#227;o dessas altera&#231;&#245;es. Com base em ecocardiogramas transtor&#225;cicos, os autores desenvolveram quatro algoritmos de aprendizado de m&#225;quina para diferenciar amiloidose card&#237;aca de outras cardiomiopatias: floresta aleat&#243;ria (RF, em ingl&#234;s), m&#225;quina de vetor de suporte (SVM, em ingl&#234;s), regress&#227;o log&#237;stica (LR, em ingl&#234;s) e &#225;rvores de decis&#227;o impulsionadas por gradiente (GBDT, em ingl&#234;s).</p>
          <p>Na popula&#231;&#227;o analisada, todos os modelos conseguiram distinguir de forma eficaz casos de amiloidose card&#237;aca de doen&#231;as n&#227;o amiloides. O modelo de LR apresentou o melhor desempenho diagn&#243;stico, superando o m&#233;todo ultrassonogr&#225;fico tradicional (AUC: RF 0,77; SVM 0,81; LR 0,81; GBDT 0,71). Os autores propuseram, portanto, a aplica&#231;&#227;o dessa ferramenta como m&#233;todo diagn&#243;stico n&#227;o invasivo para amiloidose mioc&#225;rdica. Entretanto, o n&#250;mero relativamente pequeno de casos de amiloidose card&#237;aca pode ter limitado a sensibilidade do modelo para discrimina&#231;&#227;o entre os grupos.</p>
          <p>Cotella et al.<sup><xref ref-type="bibr" rid="B2">2</xref></sup> desenvolveram um modelo de IA voltado &#224; avalia&#231;&#227;o automatizada da fra&#231;&#227;o de eje&#231;&#227;o do VE (FEVE) e do <italic>strain</italic> longitudinal global (SLG), par&#226;metros centrais no diagn&#243;stico da amiloidose card&#237;aca. Os autores justificaram a incorpora&#231;&#227;o da IA com base no fato de que as medi&#231;&#245;es manuais s&#227;o demoradas e apresentam variabilidade inter e intraobservador significativa, o que pode comprometer a precis&#227;o diagn&#243;stica e influenciar decis&#245;es terap&#234;uticas. O estudo demonstrou que as medi&#231;&#245;es automatizadas e quantitativas de FEVE e SLG apresentaram alta precis&#227;o e permitiram a detec&#231;&#227;o sens&#237;vel e espec&#237;fica de anormalidades quando comparadas &#224; an&#225;lise manual convencional, tanto em exames realizados antes do diagn&#243;stico de amiloidose card&#237;aca quanto no momento do diagn&#243;stico. N&#227;o foram observadas diferen&#231;as estatisticamente significativas entre os valores obtidos pelos dois m&#233;todos no per&#237;odo pr&#233;-diagn&#243;stico (FEVE: p = 0,791; SLG: p = 0,105) nem no momento do diagn&#243;stico (FEVE: p = 0,463; SLG: p = 0,722). Al&#233;m disso, verificou-se forte correla&#231;&#227;o entre as medi&#231;&#245;es automatizadas e manuais nos ecocardiogramas realizados antes do diagn&#243;stico (r = 0,78 para FEVE; r = 0,83 para SLG) e no diagn&#243;stico estabelecido (r = 0,74 para FEVE; r = 0,80 para SLG).</p>
          <p>Goto et al.,<sup><xref ref-type="bibr" rid="B3">3</xref></sup> embora reconhe&#231;am que modelos baseados em ECG apresentam resultados encorajadores, ressaltam que seu desempenho pode n&#227;o ser suficiente para o diagn&#243;stico de doen&#231;as de baixa preval&#234;ncia. Nesse contexto, o modelo ecocardiogr&#225;fico desenvolvido pelos autores demonstrou maior precis&#227;o preditiva quando comparado ao modelo baseado em ECG. As estat&#237;sticas C variaram de 0,85-0,91 para o ECG e de 0,89-1,00 para a ecocardiografia. Al&#233;m disso, na an&#225;lise por subtipos, o modelo apresentou desempenho superior na identifica&#231;&#227;o da amiloidose por ATTR.</p>
          <p>Em uma popula&#231;&#227;o mais espec&#237;fica, Shiri et al.<sup><xref ref-type="bibr" rid="B4">4</xref></sup> avaliaram o uso de aprendizado de m&#225;quina para detec&#231;&#227;o de amiloidose por ATTR em pacientes com estenose a&#243;rtica grave. Embora diferentes modalidades diagn&#243;sticas sejam &#250;teis na avalia&#231;&#227;o inicial desses pacientes, elas n&#227;o s&#227;o espec&#237;ficas para amiloidose por ATTR. Frequentemente, o diagn&#243;stico definitivo de cardiomiopatia por ATTR depende de confirma&#231;&#227;o histopatol&#243;gica ou da identifica&#231;&#227;o de muta&#231;&#227;o no gene <italic>TTR</italic>, associada &#224; evid&#234;ncia de capta&#231;&#227;o mioc&#225;rdica significativa na cintilografia com tra&#231;adores &#243;sseos. Considerando o custo elevado de testes gen&#233;ticos e da cintilografia com tra&#231;adores &#243;sseos, especialmente nesse grupo de pacientes, os autores desenvolveram modelo n&#227;o invasivo e potencialmente custo-efetivo, baseado em dados cl&#237;nicos e ecocardiogr&#225;ficos de rotina. O desempenho foi satisfat&#243;rio quando comparado a vari&#225;veis cl&#237;nicas, laboratoriais e de imagem intervencionista, com AUC de 0,79, sensibilidade de 0,80 e especificidade de 0,78.</p>
          <p>Eckstein et al.,<sup><xref ref-type="bibr" rid="B7">7</xref></sup> fundamentados em evid&#234;ncias de que a an&#225;lise da deforma&#231;&#227;o mioc&#225;rdica fornece valor discriminativo em m&#250;ltiplas c&#226;maras card&#237;acas, desenvolveram modelo supervisionado capaz de diferenciar amiloidose card&#237;aca de cardiomiopatia hipertr&#243;fica e de indiv&#237;duos saud&#225;veis. O sistema apresentou desempenho elevado (AUC = 0,996; precis&#227;o = 94%; sensibilidade = 100%; <italic>F1-score</italic> = 97%), indicando que a an&#225;lise automatizada da deforma&#231;&#227;o e fun&#231;&#227;o card&#237;aca multic&#226;mara pode atuar como ferramenta de suporte &#224; decis&#227;o cl&#237;nica, inclusive sem necessidade de contraste.</p>
          <p>Com a evolu&#231;&#227;o tecnol&#243;gica dos m&#233;todos de imagem cardiovascular, novas abordagens t&#234;m sido propostas para o rastreio de cardiopatias infiltrativas. Nesse contexto, Barbieri et al.<sup><xref ref-type="bibr" rid="B11">11</xref></sup> desenvolveram modelo baseado em ecocardiograma transtor&#225;cico tridimensional (ETT-3D) associado &#224; IA, com o objetivo de diferenciar diversos fen&#243;tipos de hipertrofia card&#237;aca, incluindo amiloidose card&#237;aca. O m&#233;todo prop&#245;e reformula&#231;&#227;o da an&#225;lise da fra&#231;&#227;o de eje&#231;&#227;o, tradicionalmente baseada em RMC, por meio da utiliza&#231;&#227;o do ETT-3D integrado a sistema de IA. A aquisi&#231;&#227;o tridimensional permitiu an&#225;lise mais detalhada e precisa do volume do VE, possibilitando c&#225;lculo mais acurado da fra&#231;&#227;o de eje&#231;&#227;o, definida como a raz&#227;o entre o volume sist&#243;lico e o volume diast&#243;lico final, refletindo a capacidade contr&#225;til mioc&#225;rdica. Essa abordagem fornece informa&#231;&#245;es mais precisas sobre encurtamento e espessura da parede mioc&#225;rdica, aspectos fundamentais para o reconhecimento de cardiomiopatias infiltrativas. No ecocardiograma bidimensional convencional, o aumento da espessura parietal pode mascarar redu&#231;&#227;o do encurtamento mioc&#225;rdico, resultando em fra&#231;&#227;o de eje&#231;&#227;o aparentemente preservada. No contexto da investiga&#231;&#227;o etiol&#243;gica da ICFEp, o modelo mostrou-se promissor, apresentando fra&#231;&#227;o de eje&#231;&#227;o mais elevada em pacientes com cardiomiopatia hipertr&#243;fica e com amiloidose card&#237;aca, sendo que estes &#250;ltimos exibiram valores proporcionalmente ainda maiores. O desempenho diagn&#243;stico foi consistente, com sensibilidade de 87%, especificidade de 100% e AUC de 0,959, refor&#231;ando o potencial da integra&#231;&#227;o entre ETT-3D e IA na diferencia&#231;&#227;o fenot&#237;pica da hipertrofia mioc&#225;rdica.</p>
        </sec>
        <sec>
          <title>Intelig&#234;ncia artificial na avalia&#231;&#227;o da tomografia por emiss&#227;o de p&#243;sitrons</title>
          <p>De maneira semelhante a outras modalidades de imagem, a PET-CT tem sido aprimorada com o objetivo de tornar o processo diagn&#243;stico da amiloidose card&#237;aca menos invasivo e mais preciso. Nesse contexto, destacam-se modelos baseados em <italic>deep learning</italic> voltados ao reconhecimento automatizado de padr&#245;es de imagem relacionados &#224; deposi&#231;&#227;o amiloide.</p>
          <p>Santarelli et al.<sup><xref ref-type="bibr" rid="B12">12</xref></sup> desenvolveram modelo com o objetivo de identificar, de forma r&#225;pida, precoce e espec&#237;fica, a presen&#231;a de amiloidose card&#237;aca e seus subtipos. O sistema demonstrou desempenho superior ao da an&#225;lise realizada por especialista com mais de 10 anos de experi&#234;ncia, apresentando sensibilidade superior a 0,8 e especificidade superior a 0,89. O modelo foi capaz de estimar a probabilidade de correla&#231;&#227;o entre a imagem analisada e cada subtipo de amiloidose card&#237;aca. Os autores tamb&#233;m destacaram o risco de sobreajuste (<italic>overfitting</italic>), especialmente em cen&#225;rios com n&#250;mero reduzido de imagens para treinamento. Nesse caso, o algoritmo pode apresentar desempenho elevado nos dados utilizados para treinamento, mas falhar na generaliza&#231;&#227;o para conjuntos externos. Para mitigar esse risco, foram empregadas estrat&#233;gias como aumento artificial do conjunto de dados (<italic>data augmentation</italic>) e valida&#231;&#227;o cruzada, o que contribuiu para maior robustez do modelo.</p>
          <p>No estudo de Miller et al.,<sup><xref ref-type="bibr" rid="B13">13</xref></sup> reconhece-se que a interpreta&#231;&#227;o visual da SPECT constitui padr&#227;o na avalia&#231;&#227;o diagn&#243;stica da amiloidose por ATTR, embora apresente car&#225;ter subjetivo. Os autores avaliaram abordagem de <italic>deep learning</italic> para quantifica&#231;&#227;o volum&#233;trica automatizada de tecn&#233;cio-99m (<sup>99m</sup>Tc)-pirofosfato, utilizando segmenta&#231;&#227;o de estruturas anat&#244;micas co-registradas em mapas de atenua&#231;&#227;o da tomografia computadorizada em pacientes com suspeita de amiloidose por ATTR. Os resultados demonstraram que a segmenta&#231;&#227;o baseada em <italic>deep learning</italic> n&#227;o foi influenciada pelo padr&#227;o de capta&#231;&#227;o do radiotra&#231;ador e permitiu quantifica&#231;&#227;o autom&#225;tica de imagens de capta&#231;&#227;o focal, como as obtidas com <sup>99m</sup>Tc-pirofosfato. O modelo apresentou desempenho elevado (AUC = 0,989; IC 95%: 0,974-1,00), indicando potencial para identifica&#231;&#227;o precisa de pacientes amiloidose por ATTR. Portanto, tal abordagem apresenta potencial de ser usada na identifica&#231;&#227;o precisa de pacientes com amiloidose por ATTR.</p>
        </sec>
        <sec>
          <title>Desempenho da intelig&#234;ncia artificial na avalia&#231;&#227;o da cintilografia com tra&#231;adores &#243;sseos</title>
          <p>No contexto do diagn&#243;stico da amiloidose card&#237;aca por meio da aplica&#231;&#227;o de IA na an&#225;lise de exames de imagem, &#233; poss&#237;vel estruturar sistemas integrados aos prontu&#225;rios eletr&#244;nicos, de forma semelhante ao modelo descrito por Huda et al.,<sup><xref ref-type="bibr" rid="B8">8</xref></sup> por&#233;m direcionados &#224; interpreta&#231;&#227;o automatizada de imagens cintilogr&#225;ficas.</p>
          <p>Delbarre et al.<sup><xref ref-type="bibr" rid="B14">14</xref></sup> propuseram modelo de <italic>deep learning</italic> para an&#225;lise automatizada de cintilografia com tra&#231;adores &#243;sseos de corpo inteiro com <sup>99m</sup>Tc, fundamentado na premissa de que capta&#231;&#227;o card&#237;aca significativa nesses exames &#233; fortemente sugestiva de amiloidose por ATTR. O modelo apresentou sensibilidade de 98,9% e especificidade de 99,5% na valida&#231;&#227;o cruzada. Na valida&#231;&#227;o externa, observou-se discreta redu&#231;&#227;o da sensibilidade para 96,1%, mantendo-se especificidade de 99,5%, com AUC de 0,999 em ambas as etapas.</p>
          <p>Para o desenvolvimento do sistema, utilizou-se como vari&#225;vel preditora a capta&#231;&#227;o card&#237;aca &#8805; 2 segundo a escala de classifica&#231;&#227;o de Perugini. O algoritmo foi treinado por meio de CNNs, utilizando r&#243;tulos em n&#237;vel de imagem extra&#237;dos de exames registrados nos prontu&#225;rios eletr&#244;nicos, permitindo a identifica&#231;&#227;o automatizada de padr&#245;es sugestivos de amiloidose card&#237;aca. Assim como ressaltado por Casta&#241;o et al.,<sup><xref ref-type="bibr" rid="B9">9</xref></sup> a integra&#231;&#227;o entre IA e sistemas de prontu&#225;rio favorece rastreio eficiente de condi&#231;&#245;es frequentemente sub-reconhecidas, como a associa&#231;&#227;o entre capta&#231;&#227;o card&#237;aca elevada na cintilografia com tra&#231;adores &#243;sseos de corpo inteiro e amiloidose por ATTR, contribuindo para identifica&#231;&#227;o em est&#225;gios mais precoces.</p>
          <p>Embora a cintilografia com tra&#231;adores &#243;sseos n&#227;o substitua integralmente todos os m&#233;todos diagn&#243;sticos, Delbarre et al.<sup><xref ref-type="bibr" rid="B14">14</xref></sup> destacaram que, quando ela &#233; positiva e n&#227;o h&#225; evid&#234;ncia de gamopatia monoclonal, o exame pode permitir diagn&#243;stico n&#227;o invasivo definitivo de cardiomiopatia por ATTR, especialmente em pacientes idosos ou fragilizados, nos quais a bi&#243;psia mioc&#225;rdica apresenta maior risco.</p>
          <p>Considerando que o diagn&#243;stico de amiloidose card&#237;aca pode ser estabelecido de forma n&#227;o invasiva por meio da cintilografia com tra&#231;adores &#243;sseos e que a avalia&#231;&#227;o visual &#233; inerentemente subjetiva, podendo resultar em interpreta&#231;&#245;es equivocadas, Spielvogel et al.<sup><xref ref-type="bibr" rid="B15">15</xref></sup> desenvolveram um sistema de IA para triagem padronizada e reprodut&#237;vel da doen&#231;a. O modelo foi treinado a partir de banco de dados multinacional de cintilografia com tra&#231;adores &#243;sseos marcados com <sup>99m</sup>Tc, abrangendo diferentes tra&#231;adores e <italic>scanners</italic>. Na coorte austr&#237;aca, a valida&#231;&#227;o cruzada demonstrou AUC de 1,00 (IC 95%: 1,00-1,00). Na valida&#231;&#227;o externa, os resultados permaneceram elevados, com AUC de 0,997 (IC 95%: 0,993-0,999) no Reino Unido, 0,925 (IC 95%: 0,871-0,971) na China e 1,00 (IC 95%: 0,999-1,000) nas coortes italianas. Considerando que h&#225; cerca de uma d&#233;cada, a biopsia mioc&#225;rdica representa a &#250;nica modalidade para diagnosticar amiloidose card&#237;aca, a cintilografia com tra&#231;adores &#243;sseos representa um marco no avan&#231;o do diagn&#243;stico da amiloidose card&#237;aca, principalmente quando somada &#224; IA. At&#233; aproximadamente 1 d&#233;cada atr&#225;s, a bi&#243;psia mioc&#225;rdica representava a &#250;nica modalidade definitiva para o diagn&#243;stico de amiloidose card&#237;aca. A consolida&#231;&#227;o da cintilografia com tra&#231;adores &#243;sseos constituiu avan&#231;o significativo nesse cen&#225;rio, sobretudo no diagn&#243;stico da amiloidose por ATTR. A incorpora&#231;&#227;o da IA a essa modalidade amplia ainda mais seu potencial, ao reduzir a subjetividade da interpreta&#231;&#227;o e aumentar a padroniza&#231;&#227;o e a confiabilidade diagn&#243;stica.</p>
          <p>No referido estudo multic&#234;ntrico, a capta&#231;&#227;o card&#237;aca intensa foi identificada de forma automatizada e consistente em todos os tra&#231;adores utilizados na investiga&#231;&#227;o da amiloidose card&#237;aca. Adicionalmente, a triagem baseada em IA para detec&#231;&#227;o de capta&#231;&#227;o sugestiva de amiloidose card&#237;aca em pacientes submetidos &#224; cintilografia com tra&#231;adores &#243;sseos de corpo inteiro configura ferramenta potencialmente valiosa para a identifica&#231;&#227;o precoce da doen&#231;a e para a otimiza&#231;&#227;o dos fluxos assistenciais. Nesse contexto, a implementa&#231;&#227;o dessa estrat&#233;gia pode favorecer o encaminhamento oportuno para avalia&#231;&#227;o especializada e possibilitar in&#237;cio mais precoce de terapias modificadoras da doen&#231;a, com potencial impacto na redu&#231;&#227;o da mortalidade.</p>
        </sec>
        <sec>
          <title>Intelig&#234;ncia artificial na avalia&#231;&#227;o da resson&#226;ncia magn&#233;tica card&#237;aca</title>
          <p>A RMC com realce tardio pelo gadol&#237;nio (RTG) constitui m&#233;todo fundamental na investiga&#231;&#227;o da amiloidose card&#237;aca, dada a capacidade de demonstrar altera&#231;&#245;es morfol&#243;gicas e padr&#245;es de realce caracter&#237;sticos. Entretanto, sua utiliza&#231;&#227;o pode ser limitada em pacientes com insufici&#234;ncia renal significativa, condi&#231;&#227;o frequentemente associada &#224; amiloidose, devido ao risco relacionado ao uso de contraste.</p>
          <p>Ma et al.<sup><xref ref-type="bibr" rid="B16">16</xref></sup> investigaram a viabilidade do diagn&#243;stico por meio de RMC sem contraste, utilizando mapeamento de T1 nativo associado a an&#225;lise radi&#244;mica automatizada baseada em IA. O modelo foi treinado para reconhecer padr&#245;es espec&#237;ficos de deposi&#231;&#227;o amiloide e estimar, de forma indireta, o volume extracelular (VEC), par&#226;metro tradicionalmente calculado a partir de sequ&#234;ncias pr&#233; e p&#243;s-contraste com gadol&#237;nio. Na abordagem proposta, o VEC foi estimado com precis&#227;o por meio da identifica&#231;&#227;o automatizada das regi&#245;es de interesse mioc&#225;rdicas. O modelo apresentou precis&#227;o de 86%, sensibilidade de 94%, especificidade de 85% e AUC de 0,915 no conjunto de teste. Diferentemente da cintilografia com tra&#231;adores &#243;sseos, cuja principal aplicabilidade se concentra na identifica&#231;&#227;o de amiloidose por ATTR, a RMC sem contraste demonstrou potencial para diagn&#243;stico efetivo da amiloidose card&#237;aca, particularmente na amiloidose por AL.</p>
          <p>Em conson&#226;ncia com tal perspectiva, Nowak et al.<sup><xref ref-type="bibr" rid="B17">17</xref></sup> destacaram que o valor diagn&#243;stico da RMC decorre de sua capacidade de integrar m&#250;ltiplas sequ&#234;ncias para avalia&#231;&#227;o detalhada da fun&#231;&#227;o mioc&#225;rdica, edema, inflama&#231;&#227;o e fibrose. O VEC, nesse contexto, permite quantifica&#231;&#227;o n&#227;o invasiva da deposi&#231;&#227;o amiloide mioc&#225;rdica e pode influenciar decis&#245;es terap&#234;uticas.</p>
          <p>Considerando que a RMC &#233; modalidade de refer&#234;ncia para o diagn&#243;stico de amiloidose card&#237;aca, Agibetov et al.<sup><xref ref-type="bibr" rid="B18">18</xref></sup> observaram que seus achados podem ser inespec&#237;ficos, especialmente em centros com menor volume de casos. Para minimizar esse risco, desenvolveram algoritmo baseado em CNNs aplicado a uma coorte de 502 pacientes. Independentemente da t&#233;cnica de <italic>deep learning</italic> empregada, os modelos treinados com imagens de RTG apresentaram melhor desempenho. O ajuste fino (<italic>fine-tuning</italic>) do modelo resultou em AUC de 0,96, sensibilidade de 94% e especificidade de 90%. A classifica&#231;&#227;o automatizada apresentou desempenho semelhante ao de especialistas humanos. Contudo, por se tratar de estudo unic&#234;ntrico, a generaliza&#231;&#227;o dos resultados requer cautela.</p>
          <p>Martini et al.<sup><xref ref-type="bibr" rid="B19">19</xref></sup> tamb&#233;m utilizaram <italic>deep learning</italic> para an&#225;lise automatizada de imagens de RMC e estimativa da probabilidade de amiloidose card&#237;aca. Entre os achados mais espec&#237;ficos, destacaram o padr&#227;o de pseudo-hipertrofia biventricular associado a RTG transmural difuso. A an&#225;lise automatizada de sequ&#234;ncias de RTG nas proje&#231;&#245;es 2C, 4C e eixo curto mostrou-se mais r&#225;pida e apresentou acur&#225;cia semelhante &#224; avalia&#231;&#227;o especializada, com AUC de 0,982, valor preditivo positivo de 83%, <italic>recall</italic> de 95% e <italic>F1-score</italic> de 89%.</p>
        </sec>
        <sec>
          <title>Desempenho da intelig&#234;ncia artificial na avalia&#231;&#227;o de testes gen&#233;ticos e bi&#243;psias</title>
          <p>Outro campo promissor na aplica&#231;&#227;o da IA ao diagn&#243;stico da amiloidose card&#237;aca, especialmente na forma por AL, envolve a sistematiza&#231;&#227;o da an&#225;lise de testes gen&#233;ticos voltados &#224; identifica&#231;&#227;o de muta&#231;&#245;es som&#225;ticas em cadeias leves de imunoglobulinas. Garofalo et al.<sup><xref ref-type="bibr" rid="B20">20</xref></sup> demonstraram, por meio de modelo de aprendizado de m&#225;quina, associa&#231;&#227;o entre muta&#231;&#245;es som&#225;ticas adquiridas durante a matura&#231;&#227;o dos linf&#243;citos B e o desenvolvimento de amiloidose card&#237;aca. Essas muta&#231;&#245;es afetam a estabilidade estrutural das cadeias leves, favorecendo o dobramento incorreto da prote&#237;na e a consequente forma&#231;&#227;o de dep&#243;sitos amiloides. O modelo apresentado obteve sensibilidade de 76%, especificidade de 82% e AUC de 0,87, evidenciando capacidade preditiva relevante na identifica&#231;&#227;o de sequ&#234;ncias consideradas t&#243;xicas. Al&#233;m disso, os autores destacaram que a revers&#227;o dessas muta&#231;&#245;es pode abolir o fen&#243;tipo t&#243;xico, refor&#231;ando a import&#226;ncia da caracteriza&#231;&#227;o molecular detalhada.</p>
          <p>Considerando a diversidade das sequ&#234;ncias patog&#234;nicas envolvidas, o uso de IA configura estrat&#233;gia apropriada para organizar e analisar grande volume de vari&#225;veis gen&#233;ticas, atuando como preditor de toxicidade. Dessa forma, o algoritmo pode identificar perfis moleculares associados a maior risco de desenvolvimento de amiloidose card&#237;aca, contribuindo assim para estratifica&#231;&#227;o de risco e potencial diagn&#243;stico precoce.</p>
          <p>No &#226;mbito da histopatologia, a bi&#243;psia permanece como evid&#234;ncia diagn&#243;stica definitiva na cardiomiopatia amiloide, apesar de seu car&#225;ter invasivo. Nesse contexto, a integra&#231;&#227;o entre t&#233;cnicas histol&#243;gicas e <italic>deep learning</italic> tamb&#233;m tem se mostrado promissora. Yang et al.<sup><xref ref-type="bibr" rid="B21">21</xref></sup> propuseram abordagem baseada em rede neural capaz de transformar imagens de autofluoresc&#234;ncia em imagens equivalentes &#224;s obtidas por microscopia de campo claro e luz polarizada, simulando o efeito da colora&#231;&#227;o pelo vermelho Congo.</p>
          <p>Atualmente, o padr&#227;o-ouro diagn&#243;stico baseia-se na identifica&#231;&#227;o de birrefring&#234;ncia sob luz polarizada cruzada ap&#243;s colora&#231;&#227;o com vermelho Congo. Entretanto, esse processo &#233; influenciado por variabilidade t&#233;cnica na colora&#231;&#227;o, qualidade do preparo das l&#226;minas e disponibilidade de equipamentos adequados, al&#233;m de envolver custos elevados. O modelo proposto por Yang et al.<sup><xref ref-type="bibr" rid="B21">21</xref></sup> demonstrou que as imagens geradas digitalmente apresentaram qualidade compar&#225;vel &#224;s l&#226;minas coradas convencionalmente, com potencial redu&#231;&#227;o de custos, menor depend&#234;ncia t&#233;cnica e melhor armazenamento digital das amostras, considerando que <italic>scanners</italic> especializados para captura de birrefring&#234;ncia nem sempre est&#227;o dispon&#237;veis.</p>
          <p>Assim, embora haja crescente interesse em m&#233;todos diagn&#243;sticos n&#227;o invasivos para amiloidose card&#237;aca, os avan&#231;os na aplica&#231;&#227;o da IA &#224; an&#225;lise gen&#233;tica e histopatol&#243;gica tamb&#233;m representam contribui&#231;&#227;o relevante, o que melhora a precis&#227;o diagn&#243;stica e a padroniza&#231;&#227;o dos processos laboratoriais.</p>
        </sec>
        <sec>
          <title>Barreiras de implementa&#231;&#227;o da intelig&#234;ncia artificial no fluxo de trabalho da medicina</title>
          <p>A implementa&#231;&#227;o da IA na pr&#225;tica m&#233;dica apresenta potencial significativo para ampliar a precis&#227;o diagn&#243;stica, otimizar processos assistenciais, reduzir custos e apoiar a tomada de decis&#227;o cl&#237;nica. Contudo, sua incorpora&#231;&#227;o ao fluxo de trabalho enfrenta desafios multifatoriais que podem ser agrupados em dimens&#245;es t&#233;cnicas, &#233;ticas, organizacionais e humanas.</p>
          <p>Do ponto de vista t&#233;cnico, os modelos de IA dependem de bases de dados estruturadas, completas e padronizadas. Entretanto, muitos sistemas de sa&#250;de ainda operam com registros fragmentados, inconsistentes ou incompletos, o que compromete o treinamento adequado e a capacidade de generaliza&#231;&#227;o dos algoritmos. Al&#233;m disso, dados historicamente enviesados podem perpetuar desigualdades assistenciais, resultando em recomenda&#231;&#245;es inadequadas para determinados grupos populacionais. A interoperabilidade entre diferentes sistemas de informa&#231;&#227;o tamb&#233;m constitui desafio relevante, dificultando a integra&#231;&#227;o fluida da IA aos ambientes cl&#237;nicos j&#225; estabelecidos.</p>
          <p>Sob a perspectiva &#233;tica e legal, emergem questionamentos quanto &#224; responsabiliza&#231;&#227;o em caso de erro cl&#237;nico envolvendo recomenda&#231;&#245;es algor&#237;tmicas. A defini&#231;&#227;o de responsabilidade entre desenvolvedores, institui&#231;&#245;es e profissionais permanece complexa. Soma-se a isso a preocupa&#231;&#227;o com privacidade, seguran&#231;a e governan&#231;a de dados, especialmente quando h&#225; compartilhamento interinstitucional para treinamento ou valida&#231;&#227;o de modelos.</p>
          <p>No &#226;mbito organizacional, a ado&#231;&#227;o de ferramentas baseadas em IA exige integra&#231;&#227;o eficiente aos fluxos assistenciais. Solu&#231;&#245;es que adicionam etapas ao processo ou interrompem rotinas consolidadas tendem a gerar resist&#234;ncia e sobrecarga operacional. Al&#233;m disso, &#233; imprescind&#237;vel que m&#233;dicos, enfermeiros e demais profissionais sejam capacitados para interpretar criticamente as recomenda&#231;&#245;es fornecidas pelos sistemas, utilizando-as como suporte e n&#227;o como substitui&#231;&#227;o do julgamento cl&#237;nico. A implementa&#231;&#227;o tamb&#233;m demanda investimentos em infraestrutura tecnol&#243;gica, manuten&#231;&#227;o e atualiza&#231;&#227;o cont&#237;nua dos modelos, o que pode representar barreira financeira para determinadas institui&#231;&#245;es.</p>
          <p>Por fim, a dimens&#227;o humana envolve aspectos relacionados &#224; aceita&#231;&#227;o profissional e &#224; confian&#231;a do paciente. Parte dos profissionais pode manifestar desconfian&#231;a quanto &#224; tecnologia ou perceber a IA como amea&#231;a ao seu papel cl&#237;nico. A chamada "caixa-preta" dos algoritmos, em que o processo decis&#243;rio n&#227;o &#233; plenamente transparente, pode reduzir a confian&#231;a na ferramenta e dificultar sua incorpora&#231;&#227;o &#224; pr&#225;tica cl&#237;nica. Do ponto de vista do paciente, a confian&#231;a em decis&#245;es influenciadas por algoritmos ainda n&#227;o &#233; universal. Em contrapartida, h&#225; risco de depend&#234;ncia excessiva da IA por parte dos profissionais, o que pode comprometer o exerc&#237;cio do racioc&#237;nio cl&#237;nico independente caso n&#227;o haja postura cr&#237;tica e reflexiva.</p>
        </sec>
      </sec>
      <sec sec-type="conclusions">
        <title>Conclus&#227;o</title>
        <p>Com base nos achados desta revis&#227;o, a IA configura-se como ferramenta promissora na otimiza&#231;&#227;o do rastreio e do diagn&#243;stico da amiloidose card&#237;aca. Sua aplica&#231;&#227;o em diferentes modalidades diagn&#243;sticas demonstra potencial para acelerar a identifica&#231;&#227;o da doen&#231;a, contribuir para maior precis&#227;o diagn&#243;stica e, consequentemente, favorecer melhores desfechos cl&#237;nicos.</p>
        <p>A elevada capacidade de processamento e an&#225;lise de grandes volumes de dados permite &#224; IA reconhecer padr&#245;es complexos, ampliar sua capacidade de generaliza&#231;&#227;o, desde que treinada com bases robustas e representativas, e auxiliar na detec&#231;&#227;o precoce da amiloidose card&#237;aca. Ademais, a utiliza&#231;&#227;o de modelos automatizados pode reduzir a subjetividade da interpreta&#231;&#227;o humana, minimizar a necessidade de procedimentos invasivos em determinados contextos e racionalizar o uso de recursos em sa&#250;de.</p>
        <p>Entretanto, apesar dos avan&#231;os observados, a consolida&#231;&#227;o da IA na pr&#225;tica cl&#237;nica exige aprimoramento cont&#237;nuo dos modelos, valida&#231;&#227;o externa em popula&#231;&#245;es diversas e integra&#231;&#227;o eficiente aos fluxos assistenciais. S&#227;o igualmente fundamentais o planejamento estrat&#233;gico da implementa&#231;&#227;o, a capacita&#231;&#227;o dos profissionais de sa&#250;de, a governan&#231;a &#233;tica no manejo de dados e o monitoramento permanente do desempenho algor&#237;tmico.</p>
      </sec>
    </body>
    <back>
      <fn-group>
        <fn fn-type="financial-disclosure" id="fn5">
          <label>Fontes de Financiamento</label>
          <p>O presente estudo n&#227;o teve fontes de financiamento externas.</p>
        </fn>
        <fn fn-type="other" id="fn6">
          <label>Vincula&#231;&#227;o Acad&#234;mica</label>
          <p>N&#227;o h&#225; vincula&#231;&#227;o deste estudo a programas de p&#243;s-gradua&#231;&#227;o.</p>
        </fn>
        <fn fn-type="other" id="fn7">
          <label>Aprova&#231;&#227;o &#201;tica e Consentimento Informado</label>
          <p>Este artigo n&#227;o cont&#233;m estudos com humanos ou animais realizados por nenhum dos autores.</p>
        </fn>
        <fn fn-type="other" id="fn8">
          <label>Uso de Intelig&#234;ncia Artificial</label>
          <p>Os autores n&#227;o utilizaram ferramentas de intelig&#234;ncia artificial no desenvolvimento deste trabalho.</p>
        </fn>
      </fn-group>
      <sec sec-type="data-availability" specific-use="data-in-article">
        <title>Disponibilidade de Dados</title>
        <p>Os conte&#250;dos subjacentes ao texto da pesquisa est&#227;o contidos no manuscrito.</p>
      </sec>
    </back>
  </sub-article>
</article>
