ijcs International Journal of Cardiovascular Sciences Int J Cardiovasc Sci 2359-4802 2359-5647 Sociedade Brasileira de Cardiologia rL73LrJrrbNL6tFVXhCrvHv S2359-56472024000100309 00309 10.36660/ijcs.20240082 REVIEW ARTICLE The Role of Strain in the Prognosis of Transthyretin Amyloidosis 0000-0003-1985-6397 Silva Ana Karolina Bento Bento da Conception and design of the research analysis and interpretation of the data and writing of the manuscript acquisition of data 1 0009-0004-6559-3895 Cavalcanti Leonardo Torreão Bezerra Conception and design of the research analysis and interpretation of the data and writing of the manuscript acquisition of data 1 0000-0002-0711-7995 Barberato Silvio Henrique critical revision of the manuscript for intellectual content 2 0000-0001-7046-8707 Felix Alex dos Santos critical revision of the manuscript for intellectual content 3 0000-0001-8809-8783 Melo Marcelo Dantas Tavares de Conception and design of the research analysis and interpretation of the data and writing of the manuscript critical revision of the manuscript for intellectual content 1 Universidade Federal da Paraíba João Pessoa PB Brazil Universidade Federal da Paraíba, João Pessoa, PB – Brazil Centro de Diagnóstico Cardiovascular Curitiba PA Brazil Cardioeco, Centro de Diagnóstico Cardiovascular, Curitiba, PA – Brazil Instituto Nacional de Cardiologia Rio de Janeiro RJ Brazil Instituto Nacional de Cardiologia, Rio de Janeiro, RJ – Brazil Mailing Address: Ana Karolina Bento Bento da Silva Universidade Federal da Paraíba, Campus I. Loteamento, cidade universitária. Postal code: 58051-900. João Pessoa, PB – Brazil E-mail: Anakarolinabentos@gmail.com

Potential Conflict of Interest

No potential conflict of interest relevant to this article was reported.

Editor responsible for the review: Marcus Vinícius Simões

 19 08 2024 2024 37 e20240082 6 05 2024 13 05 2024 23 05 2024 This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

: The Role of Strain in the Prognosis of Transthyretin Amyloidosis LVEF: Left ventricular ejection fraction; RVFWS: Right ventricular free wall strain; RAS: Right atrium strain; GLS: global longitudinal strain; LAS: Left atrium strain; NYHA: New York Heart Association Classification of Heart Failure.

Abstract

Transthyretin amyloidosis (TTRA) is a systemic infiltrative disease where cardiac involvement is paramount for prognosis. The strain technique plays a crucial role in non-invasive cardiac screening for this condition. Research on the prognostic utility of cardiac deformation in TTRA indicates the significance of right ventricular (RV) free wall strain, global longitudinal strain (GLS), left and right atrium reservoir strain, in descending order of publication, respectively. The GLS has emerged as a promising tool for therapeutic monitoring. Analyzing myocardial deformation is vital due to its incremental value over other clinical, laboratory, and imaging parameters. However, caution is warranted due to limited data on its prognostic and therapeutic monitoring use in TTRA. Despite the strong rationale for employing myocardial deformation in patient stratification, further robust studies are necessary to establish it as a new prognostic marker in TTRA.

 Echocardiography Cardiomyopathies Heart Failure Introduction

TTRA results from the misfolding and deposition of transthyretin monomers, a tetrameric protein synthesized by the liver that normally functions to transport thyroid hormone and retinol. Among its clinical manifestations, cardiomyopathy is considered the main factor of poor prognosis, affecting approximately 50,000 to 150,000 people in the USA. In Brazil, it is estimated that there are more than 5,000 patients who have TTRA with cardiac involvement.1-3

Transthyretin amyloidosis (TTRA) is categorized in two main forms: one resulting from mutations in the transthyretin gene (TTRAv), inherited in an autosomal dominant manner, with its gene located on chromosome 18 and over 140 mutations described to date. The other form, known as wild-type TTRA (wtTTRA), involves a normal amino acid sequence, although the mechanism by which the wild-type protein becomes unstable remains not completely understood.2 This type is believed to be the most common form of TTRA amyloidosis, accounting for approximately 75% of cases and typically presenting as cardiomyopathy, with less than 10% of patients concurrently experiencing polyneuropathy.1

TTRA manifests mainly as cardiomyopathy and/or polyneuropathy, depending on the mutation and interaction of amyloid fibrils in the body. Myocardial deposition leads to progressive loss of myocardial compliance, clinically presenting as heart failure with preserved ejection fraction (HFpEF), arrhythmias, dysautonomia, and ultimately, death. In advanced stages, myocardial deposits cause severe diastolic dysfunction and a reduction in ejection fraction.1

Studies indicate that wild-type transthyretin amyloidosis (wtTTRA) is relatively common among older adults with HFpEF and severe aortic stenosis, particularly in those with low flow and low gradient.4

The suspicion of amyloidosis arises in patients with unexplained left ventricular (LV) hypertrophy, regardless of age, accompanied by various symptoms such as syncope, pre-syncope, dyspnea, angina, and signs of systemic involvement. Transthoracic echocardiography serves as the primary diagnostic tool for assessing structural changes in patients suspected of cardiac amyloidosis (CA). However, imaging faces challenges in differentiating cardiomyopathies based on phenocopies, particularly distinguishing between hypertrophic and dilated forms. With the improvement of imaging techniques, together with the genetic study being more accessible in clinical practice, it is now clear that the morphology is insufficient for a precise diagnosis. The study of cardiac mechanics, particularly in phenocopies with increased thickness, allows us to find unique patterns for each one, for which the term “fingerprint” is used.1,4

In 2012, Phelan et al. revealed that a pattern of relative apical preservation measured by Global Longitudinal Strain (GLS), compared with arterial hypertension, hypertrophic cardiomyopathy, and aortic stenosis, was both specific and sensitive for the diagnosis of CA. This characteristic is not exclusive to the LV, as the involvement of the right ventricle (RV) also presents affected mid-basal regions.5

The evolution of multimodality imaging in amyloidosis plays a central role in the diagnosis of CA, evidencing the parametric presentation of strain, which gained popularity as a synonym for amyloidosis (apical sparing, cherry on top, for example). Nevertheless, there remains a significant gap in the use of myocardial deformation analysis among these patients and its implications for prognostic stratification. In this review, the main articles on the matter will be analyzed with a critical view.

 Discussion

TTRA is generally a progressive disease with a poor prognosis when not diagnosed and treated in its early stages. Echocardiography provides information that helps predict cardiovascular outcomes in patients with TTRA. Given that LV ejection fraction often remains normal until the disease reaches advanced stages, reliance on other echocardiographic indices becomes crucial for symptom interpretation and risk stratification. Several echocardiographic indices were independently associated with higher mortality rates in TTRA, such as indexed stroke volume, indexed right atrium area, E/e´ ratio and GLS.6 In fact, subclinical dysfunction of all cardiac chambers appears to have additional prognostic significance, as strain-derived data showed an association with higher mortality.7

The position on Diagnosis and Treatment of Cardiac Amyloidosis by the Brazilian Society of Cardiology establishes that the prognosis of this disease is measured through the emergence and duration of HF symptoms. As a result, low-cost laboratory tests have been used in different proposals for staging the disease, thereby obtaining a good level of correlation with life expectancy (serum levels of troponin T and I, glomerular filtration rate, NT-proBNP). Furthermore, the evident contribution of imaging exams to the prognostic assessment of patients with TTRA converges into the same group: Echocardiogram, Cardiac Magnetic Resonance Imaging, and Myocardial Scintigraphy with Tc99. Regarding echocardiography, the document reveals the following metrics related to prognosis: LVEF, myocardial contraction fraction, GLS, and apical preservation.8

There is a consensus regarding the use of functional class, biomarkers, reduced ejection fraction, and diastolic dysfunction for prognostic stratification in these patients.9,10Table 1 summarizes the primary prognostic scores in TTRA, emphasizing the use of biomarkers.

– TTRA staging according to biomarkers.
Studies Biomarkers cut-off value Staging Prognosis (in months)
Grogan et al., 201611 wtTTRA: NT-proBNP > 3000 ng/l cTnT > 0.05 mcg/l Stage I: NT-proBNP < 3000 ng/l and/or cTnT <0.05 mcg/l Stage II: NT-proBNP OR cTnT above the cut-off value Stage III: NT-proBNP and cTnT above the cut-off value Stage I: 66 Stage II: 40 Stage III: 20
Hanson et al., 201812 wtTTRA: sTTR < 18 mg/dL Tncl < 0.049 ng/ml sTTR < 18 mg/dL sTTR > 18 mg/dL 33 49
Gillmore et al., 201813 wtTTRA, NT-proBNP > 3000 ng/l hTTRA, eGFR < 45 ml/min Stage I: NT-proBNP < 3000 ng/l and/or eGFR > 45ml/min Stage II: NT-proBNP OR eGFR > 45ml/min Stage III: NT-proBNP and eGFR > 45ml/min Stage I: 69,2 Stage II: 46,7 Stage III: 24,1

wtTTRA: Wild-type transthyretin amyloidosis; hTTRA: Hereditary transthyretin amyloidosis; Nt-proBNP: N-terminal pro-B-type natriuretic pepite; cTnT: Cardiac troponin T; cTnI: Cardiac troponin I; eGFR: estimated glomerular filtration rate; LVEF: Left ventricular ejection fraction; sTTR: Serum transthyretin dosage.

The 2023 American College of Cardiology expert consensus underscores the pivotal role of echocardiography in diagnosing TTRA, particularly in elucidating the prognostic significance of myocardial deformation.10 Given the challenges and limitations associated with clinical, laboratory, and imaging modalities, the study of cardiac chamber deformation enhances the robustness of clinical and therapeutic monitoring. Despite the growing interest in this technique, it lacks consensus regarding its use for prognosis assessment in the literature, while also not being addressed in the prognosis and follow-up guidelines of recent society publications as other strain tools for different cardiac chambers. Table 2 provides a summary of the main articles collected on the analysis of TTRA deformation and prognosis.

– Summary of evidence.
Author, date Objectives Sample Echocardiographic Parameters Findings Results
Bodez et al., 201614 To investigate the prognostic value of RV dysfunction in patients with CA. n = 82 TAPSE RVFWS TAPSE < 14mm TAPSE was found to be a prognostic marker, reflecting RV and LV involvement.
Solomon et al.,, 201915 Effects of Patisiran on cardiac structure and function in patients with CA. n = 126 LV thickness GLS LVEF GLS reduction > 2% Treatment with Patisiran resulted in reduced LV wall thickness and improved GLS compared to placebo.
Minamisawa et al, 201916 To evaluate the association of Patisiran treatment with a regional strain of the LV myocardium in the cardiac manifestation of TTRA amyloidosis. n = 126 LVGLS LVGLS improvement = 1.4% compared to placebo Patisiran prevented the deterioration of LV GLS over 18 months, mainly by attenuating disease progression in the basal region.
Fine et al., 202017 Prognostic relevance of right and left chamber function in CA. n = 97 TAPSE LVEF GLS RVFWS RVFWS reduction > 1.2% GLS reduction > 1.4% RVFWS was associated with mortality and the need for cardiovascular hospitalization. GLS changes were associated with adverse outcomes.
Huntjens et al., 20217 Prognostic value of atrial and ventricular deformation in patients with CA. n = 136 LVEF TAPSE GLS RVFWS LAS RAS LV thickness RVFWS < 17.0% GLS < 10.4% LAS < 13.2% RAS < 12.4% Decreased RVFWS, GLS, LAS, and RAS indexes showed a correlation with the chance of death: 2.8x, 2.3x, 7.5x and 3.5x greater the chance, respectively.
Tjahjadi et al., 202218 To investigate the prognosis associated with right chamber dysfunction in patients with CA. n = 93 RVFWS TAPSE RVFWS <16% The use of RVFWS was associated with an incremental prognostic value compared to conventional echocardiographic parameters such as TAPSE.
Giblin et al., 202219 Natural history of myocardial function in untreated CA, and determination of the effect of Tafamidis on myocardial functional parameters in a 12-month treatment program. n = 45 GLS Myocardial work index Myocardial efficiency GLS: -0.3% vs -1.1%* Tafamidis in TTRA-CM decreases the deterioration of cardiac function, as measured by GLS and myocardial work index over 1 year, when compared with an untreated cohort.
Usuku et al., 202220 To investigate whether GLS provides prognostic information in patients with CA. n = 129 RVFWS GLS RVFWS < 11.59% GLS has prognostic value in patients with TTRA and provides greater prognostic power compared to conventional echocardiographic findings.
Shah et al., 202421 To analyze the effect of Tafamidis on cardiac function in patients with TTRA n = 436 LVGLS LVGLS decline = 1.84% compared to placebo A mild decline was seen in LVSG with Tafamidis, 80 mg, vs. placebo in the mid and basal regions, while an attenuated decline in LV circumferential and radial strain was observed in the mid and apical regions.

TAPSE: tricuspid annular plane systolic excursion; RV: Right ventricle; LV: Left ventricle; GLS: Global longitudinal strain; LVEF: Left ventricular ejection fraction; LVGLS: Left ventricular global longitudinal strain; RVFWS: Right ventricular free wall strain; LAS: Left atrium strain; RAS: Right atrium strain; TTRA: Transthyretin amyloidosis; CA: cardiac amyloidosis.

RV Strain

The analysis by Peter R. Huntjens et al. corroborates the 2021 SBC position, showing that decreased GLS values were associated with a poor prognosis. The research also highlighted the significant role of right ventricular free wall strain (RVFWS) in prognostic stratification, with a decrease in this index (<17%) correlating with a 2.8-fold increase in the likelihood of cardiovascular death.7 Similarly, Nowell M. Fine et al. observed during annual follow-up that the decline in RVFWS was more pronounced in the group experiencing cardiovascular death (reduction >2%), notably lower in the TTRA group compared to patients with light chain amyloidosis (LA), thus rendering this measure more sensitive for quantifying ventricular mechanical function.17 Supporting this observation, Hiroki Usuku et al. identified free wall strain as an independent variable associated with cardiovascular death, demonstrating a sensitivity of 69.2% and specificity of 63.5%.20 Moreover, the RVFWS indicator (< 11.59%) alone was directly correlated with cardiovascular death and the number of hospitalizations for heart failure.17,20 Notably, conventional echocardiographic findings commonly linked to RV function, such as tricuspid annular plane systolic excursion (TAPSE) and fractional change in RV area (FAC-RV), did not achieve statistical significance according to the study by Hiroki Usuku et al.20 The suggested explanation for this observation stems from the potential impact of the apical movement of the LV on TAPSE, which could lead to over or underestimation of RV function based on transducer angulation.10 Conversely, Bodez et al. found TAPSE to be a significant independent predictor of major cardiac events within 6 months, unlike other parameters assessing RV systolic function. As a result, the study recommends incorporating this measurement into the routine evaluation of patients with CA, with a suggested TAPSE cut-off point of < 14 mm.14

Catherine Tjahjadi et al., while identifying TAPSE as an independently related parameter to cardiovascular death, demonstrated that RVFWS (<16%) exhibited a stronger association with all-cause mortality, offering incremental prognostic value over conventional parameters of RV systolic function.18 Therefore, two parameters of RV longitudinal systolic function emerge, with RVFWS serving as a more sensitive marker for subclinical detection and TAPSE as a more specific parameter characterized by less interobserver variability and better reproducibility. Therefore, patients may present with incipient RV involvement and normal TAPSE, although they more frequently present a reduction in RVFWS, which may be a justification for the result described. In this study, patients with reduced TAPSE apparently had more advanced disease.

 LV Strain

On echocardiography, patients with TTRA cardiomyopathy typically show increased LV wall thickness, preserved ejection fraction, different degrees of diastolic dysfunction and reduced SGL.1 The prognostic importance of the initial measurement GLS has been consolidated in patients with both cardiac amyloid subtypes, regardless of other imaging, laboratory and clinical variables.17 Barros-Gomes et al. showed that SGL provided incremental prognostic value in 61 patients with LA CA over the current validated LA staging system in patients with preserved LVEF. Thus, it was related to a worse GLS prognosis of less than 14.81%.22

The findings of Nowell M. Fine et al. corroborate other studies describing the prognostic value of GLS and demonstrating that the progressive decline of GLS during follow-up is associated with a poor prognosis (reduction > 1.4%).17 (Figure 1). In the study by Peter R. Huntjens et al., reducing this metric was associated with a 2.3-fold increase in the risk of death. In this study, the cutoff point was classified as GLS < 10.4%.7 However, the frequency, modality and ideal parameters for evaluating follow-up cardiac images of patients with CA remain uncertain.17,20

– Temporal evolution of GLS in a patient with CA, demonstrating disease progression and eventual death within 6 months. A gradual and progressive decline in GLS is evident, with a distinct presentation in the parametric analysis, notably sparing the apex.

Left Atrium Strain

The left atrium is an extremely thin chamber, which makes it a challenge for tissue analysis using imaging methods. Its involvement in amyloidosis would be intuitively attributed to LV diastolic dysfunction. However, investigations conducted on explanted hearts have revealed the presence of amyloid infiltrate, fibrosis, and disorganization of atrial fibers. Consequently, it is understood that left atrial involvement can manifest even in the absence of significantly elevated filling pressures in the LV. The analysis of left atrial deformation in amyloidosis indicates a reduction across its three phases (reservoir, conduit, and contraction).23 Notably, when assessing strain via the four-chamber view, a decrease in strain of the RV, right atrium, LV, and left atrium has been linked to poor prognosis. Interestingly, left atrial reservoir strain emerged as the most significant parameter for prognostic stratification, with a cutoff point below 13.2%.7

A prospective study from 2018 by the University Hospital of Limoges, France, using three-dimensional echocardiography, concluded that the three-dimensional strain of the left atrial reservoir (LAS) has a good correlation with the Mayo Clinic clinical stages in patients with LA amyloidosis.24 Under this perspective, the study by Peter R. Huntjens brings the study of LAS as a prognostic measure in patients with TTRA. It demonstrates that LAS is additive to GLS and independently associated with survival in patients with CA. In this study, a cutoff point of LAS < 13.2% was adopted, with a decrease in this parameter corresponding to a 7.5-fold increase in the risk of death. Thus, LAS reflects more advanced cardiac involvement in CA and, therefore, shows potential as a new prognostic marker.7

 Right Atrium Strain

Assessment of the right atrium is limited due to geometric difficulties in two-dimensional echocardiography. However, three-dimensional echocardiography is a new clinical modality that allows accurate measurement of atrial volume changes. The MAGYAR-Path study demonstrates right atrial strain (RAS) as an alternative for the evaluation of patients with AL, showing a correlation between this measurement and cardiac dysfunction.25 However, the study does not define this index as having diagnostic or prognostic value.

A study by Peter R. Huntjens et al. uses RAS as a new parameter for prognostic assessment in patients with TTRA. In this sense, RAS lower than the median of 12.4% was associated with a 3.5-fold increase in the risk of death.7

 New Tools Myocardial Work

Non-invasive assessment of myocardial work using echocardiographic software is a relatively novel approach, showing promise in the context of TTRA. However, it remains an area requiring further exploration. In the context of aortic stenosis, both with and without amyloidosis, a limited number of studies have highlighted the myocardial work index as a superior prognostic indicator for mortality compared to LV ejection fraction and GLS.26 In a single-center study involving 113 patients with wtTTRA, the myocardial work index demonstrated added prognostic value in predicting outcomes such as death and hospitalization for heart failure within this population.27

 Cardiac Elastography

The use of the elastography technique for assessing cardiac stiffness has been previously explored through cardiac magnetic resonance imaging.28 While elastography is commonly employed using ultrasound to evaluate liver stiffness in patients with cirrhosis, thus reducing the necessity for routine biopsies,29 there is a growing interest in applying this technique directly to assess cardiac stiffness. In CA, cardiac elastography has demonstrated not only a strong correlation between cardiac stiffness and various clinical, laboratory, and imaging parameters but also provides incremental prognostic value for these patients.30 This tool is expected to attract increasing attention for studies focusing on phenocopies characterized by increased thickness and reduced compliance.

 Value of Testing for the Impact of Existing Therapies

Conventional echocardiographic, clinical and biomarker indicators have been established to evaluate treatment in LA. However, the use of similar markers in the treatment of TTRA has been limited due to their variability.

The TTRA-ACT study primarily aimed to evaluate the efficacy, safety and tolerability of Tafamidis compared to placebo for the treatment of TTRA. Assessment of intervention efficacy was conducted based on the 6-minute walk test, changes in the Kansas City Cardiomyopathy Questionnaire-Overall Summary (KCCQ-OS) score, and the NYHA classification.24 In a study by Ahmed Ghoneem et al., the effectiveness of Tafamidis versus placebo was evaluated solely based on heart failure exacerbation events without incorporating objective metrics.31 Similarly, in a study by Mathew S. Maurer et al., outcomes associated with Patisiran were assessed using the 6-minute walk test, KCCQ-OS score, and composite endpoints, including all-cause mortality and heart failure-related hospitalizations.32 However, these studies did not delve into more comprehensive analyses, such as incorporating imaging modalities to evaluate therapy effectiveness.

Giblin et al. bring echocardiographic monitoring as an alternative to evaluate the impacts of drug therapy as a reproducible, objective and non-invasive method. In their analysis, they used the GLS to evaluate the impact of treatment with Tafamidis. In absolute terms, GLS deteriorated by a median of 0.3% over one year in treated patients, a rate lower than that found in patients who did not use the medication (1.1%) (Figure 2).19

– This illustration exemplifies the impact of a disease-modifying drug (Tafamidis), demonstrating reduced ventricular mass and stabilized cardiac mechanics (global longitudinal strain). GLS: Global Longitudinal Strain; SEPT: Septum; ANT: Anterior; INF: Inferior; POST: Posterior

Another study revealed that higher doses of Tafamidis at 80 mg versus placebo resulted in a mild decline LVGLS in the mid and basal regions of the LV (−1.84; 95% CI, −2.79 to −0.89; P<.001), along with a reduced decline in LV circumferential and radial strain in the mid and apical regions.33 Similar effects were subsequently observed in patients using Patisiran. In this context, a study indicated a reduction in LV wall thickness and a decrease in GLS (>2%) in the Patisiran group compared to placebo.19 Another study involving the same drug also showcased an enhancement in absolute GLS (1.4% [0.6%]; 95% CI, 0.3%-2.5%; P = 0.02) compared to placebo over an 18-month follow-up period.21

While these findings provide promising insights, they should be interpreted with caution due to the limited evidence on the efficacy of echocardiography and strain in assessing therapeutic response. This reinforces the uncertainty surrounding the categorical and systematic use of these tools for this purpose despite their strong plausibility. The central illustration summarizes the key points discussed in this review.

 Conclusion

The integration of myocardial deformation analysis holds significant importance due to its supplementary role alongside clinical, laboratory, and imaging parameters. However, cautious interpretation is warranted due to the limited data regarding its application in TTRA, particularly when employed independently. The current scenario offers a promising opportunity for future research to validate the reliability of this parameter in prognostic stratification for this condition.

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