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  <front>
    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Arq Bras Cardiol</journal-id>
      <journal-id journal-id-type="publisher-id">abc</journal-id>
      <journal-title-group>
        <journal-title>Arquivos Brasileiros de Cardiologia</journal-title>
        <abbrev-journal-title abbrev-type="publisher">Arq. Bras. Cardiol.</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0066-782X</issn>
      <issn pub-type="epub">1678-4170</issn>
      <publisher>
        <publisher-name>Sociedade Brasileira de Cardiologia - SBC</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id specific-use="scielo-v3" pub-id-type="publisher-id">K5rZpc8nCQmfPzJpmk6D6wz</article-id>
      <article-id specific-use="scielo-v2" pub-id-type="publisher-id">S0066-782X2023000300503</article-id>
      <article-id pub-id-type="other">00503</article-id>
      <article-id pub-id-type="doi">10.36660/abc.20220665</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Carta ao Editor</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Gen&#243;tipo da Paraoxonase-1 e Angiograma Positivo para Doen&#231;a Arterial Coronariana</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0003-0078-7897</contrib-id>
          <name>
            <surname>Mungmunpuntipantip</surname>
            <given-names>Rujittika</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
          <xref ref-type="corresp" rid="c1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Wiwanitkit</surname>
            <given-names>Viroj</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">
            <sup>2</sup>
          </xref>
        </contrib>
        <aff id="aff1">
          <label>1</label>
          <institution content-type="orgname">Consultor Acad&#234;mico Privado</institution>
          <addr-line>
            <named-content content-type="city">Bangkok</named-content>
          </addr-line>
          <country country="TH">Tail&#226;ndia</country>
          <institution content-type="original">Consultor Acad&#234;mico Privado, Bangkok &#8211; Tail&#226;ndia</institution>
        </aff>
        <aff id="aff2">
          <label>2</label>
          <institution content-type="orgname">Universidade Dr. DY Patil</institution>
          <addr-line>
            <named-content content-type="city">Pune</named-content>
          </addr-line>
          <country country="IN">&#205;ndia</country>
          <institution content-type="original">Universidade Dr. DY Patil, Pune &#8211; &#205;ndia</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c1"><bold>Correspond&#234;ncia: Rujittika Mungmunpuntipantip</bold> &#8226; Private Academic Consultant 111 Bangkok 122 Bangkok <postal-code>103300</postal-code> &#8211; Tail&#226;ndia. E-mail: <email>rujittika@gmail.com</email></corresp>
      </author-notes>
      <pub-date publication-format="electronic" date-type="pub">
        <day>07</day>
        <month>04</month>
        <year>2023</year>
      </pub-date>
      <pub-date publication-format="electronic" date-type="collection">
        <year>2023</year>
      </pub-date>
      <volume>120</volume>
      <issue>3</issue>
      <elocation-id>e20220665</elocation-id>
      <permissions>
        <license license-type="open-access" xml:lang="en" xlink:href="https://creativecommons.org/licenses/by/4.0/">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License</license-p>
        </license>
      </permissions>
      <kwd-group xml:lang="pt">
        <title>Palavras-chave</title>
        <kwd>Doen&#231;a Arterial Coronariana/gen&#233;tica</kwd>
        <kwd>Mortalidade</kwd>
        <kwd>Polimorfismo Gen&#233;tico</kwd>
        <kwd>Predisposi&#231;&#227;o Gen&#233;tica para Doen&#231;a</kwd>
        <kwd>Fatores de Risco</kwd>
      </kwd-group>
      <counts>
        <fig-count count="0"/>
        <table-count count="0"/>
        <equation-count count="0"/>
        <ref-count count="3"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>Prezado Editor,</bold>
    </p>
    <p>Gostar&#237;amos de compartilhar ideias sobre a publica&#231;&#227;o &#8220;Associa&#231;&#227;o do Gen&#243;tipo e Fen&#243;tipo da Paraoxonase-1 com Angiograma Positivo para Doen&#231;a Arterial Coronariana.&#8221;<sup><xref ref-type="bibr" rid="B1">1</xref></sup> Soflaei et al.,<sup><xref ref-type="bibr" rid="B1">1</xref></sup> observaram que a presen&#231;a do alelo G do polimorfismo de nucleot&#237;deo &#250;nico rs662 est&#225; independentemente associada a um risco aumentado de doen&#231;a arterial coronariana (DAC).<sup><xref ref-type="bibr" rid="B1">1</xref></sup> O efeito do polimorfismo &#233; investigado neste estudo. A DAC pode ou n&#227;o ser afetada pelo componente heredit&#225;rio estudado neste relat&#243;rio. Ambos concordamos que a DAC pode estar relacionada ao componente gen&#233;tico subjacente sob pesquisa. No entanto, a DAC tem sido associada a in&#250;meras varia&#231;&#245;es gen&#233;ticas. Exemplos de polimorfismos de genes incluem o efeito de polimorfismos (M235T e T174M) no gene do angiotensinog&#234;nio (AGT), TGFB1 rs1800469 e BCMO1 rs6564851.<sup><xref ref-type="bibr" rid="B2">2</xref>-<xref ref-type="bibr" rid="B3">3</xref></sup> Pesquisas futuras devem examinar as implica&#231;&#245;es de variantes gen&#233;ticas inesperadas e possivelmente desconcertantes.</p>
  </body>
  <back>
    <ref-list>
      <title>Refer&#234;ncias</title>
      <ref id="B1">
        <label>1</label>
        <element-citation publication-type="journal">
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            <name>
              <surname>Soflaei</surname>
              <given-names>SS</given-names>
            </name>
            <name>
              <surname>Baktashian</surname>
              <given-names>M</given-names>
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          <article-title>Association of Paraoxonase-1 Genotype and Phenotype with Angiogram Positive Coronary Artery Disease</article-title>
          <source>Arq Bras Cardiol</source>
          <year>2022</year>
          <volume>119</volume>
          <issue>4</issue>
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          <lpage>601</lpage>
          <pub-id pub-id-type="doi">10.36660/abc.20210422</pub-id>
        </element-citation>
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  </back>
  <sub-article article-type="translation" id="S01" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Letter to the Editor</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Paraoxonase-1 Genotype and Angiogram Positive Coronary Artery Disease</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0003-0078-7897</contrib-id>
          <name>
            <surname>Mungmunpuntipantip</surname>
            <given-names>Rujittika</given-names>
          </name>
          <xref ref-type="aff" rid="aff3">
            <sup>1</sup>
          </xref>
          <xref ref-type="corresp" rid="c2"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Wiwanitkit</surname>
            <given-names>Viroj</given-names>
          </name>
          <xref ref-type="aff" rid="aff4">
            <sup>2</sup>
          </xref>
        </contrib>
        <aff id="aff3">
          <label>1</label>
          <addr-line>
            <named-content content-type="city">Bangkok</named-content>
          </addr-line>
          <country country="TH">Thailand</country>
          <institution content-type="original">Private academic consultant, Bangkok &#8211; Thailand</institution>
        </aff>
        <aff id="aff4">
          <label>2</label>
          <addr-line>
            <named-content content-type="city">Pune</named-content>
          </addr-line>
          <country country="BR">India</country>
          <institution content-type="original">Universidade Dr. DY Patil, Pune &#8211; India</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c2"><bold>Mailing Address: Rujittika Mungmunpuntipantip &#8226;</bold> Private Academic Consultant 111 Bangkok 122 Bangkok <postal-code>103300</postal-code> &#8211; Thailand. E-mail: <email>rujittika@gmail.com</email></corresp>
      </author-notes>
      <kwd-group xml:lang="en">
        <title>Keywords</title>
        <kwd>Coronary Artery Disease/genetics</kwd>
        <kwd>Mortality</kwd>
        <kwd>Polymorphism, Genetic</kwd>
        <kwd>Genetic Predisposition to Disease</kwd>
        <kwd>Risk Factors</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>Dear Editor,</bold>
      </p>
      <p>We would like to share ideas on the publication &#8220;Association of Paraoxonase-1 Genotype and Phenotype with Angiogram Positive Coronary Artery Disease&#8221;. <sup><xref ref-type="bibr" rid="B1">1</xref></sup> Soflaei et al.<sup><xref ref-type="bibr" rid="B1">1</xref></sup> noted that The presence of the G allele of the rs662 single nucleotide polymorphism is independently associated with an increased risk of coronary artery disease (CAD).<sup><xref ref-type="bibr" rid="B1">1</xref></sup> The effect of polymorphism is investigated in this study. CAD might or might not be impacted by the hereditary component studied in this report. We both concur that CAD may be related to the underlying genetic component under research. However, CAD has been linked to numerous genetic variations. Examples of gene polymorphisms include the effect of polymorphisms (M235T and T174M) on the angiotensinogen gene (AGT), TGFB1 rs1800469, and BCMO1 rs6564851.<sup><xref ref-type="bibr" rid="B2">2</xref>-<xref ref-type="bibr" rid="B3">3</xref></sup> Future research should examine the implications of unexpected, possibly perplexing genetic variants.</p>
    </body>
  </sub-article>
</article>
