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Arquivos Brasileiros de Cardiologia
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Arquivos Brasileiros de Cardiologia
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Speckle Tracking and Transthyretin Amyloid Cardiomyopathy

Authors: Rocha, Alexandre Marins; Ferreira, Suzane Garcia; Nacif, Marcelo Souto; Ribeiro, Mario Luiz; Freitas, Marcos Raimundo Gomes de; Mesquita, Cláudio Tinoco;

Speckle Tracking and Transthyretin Amyloid Cardiomyopathy

Abstract

Amyloidosis is a disease caused by deposits of insoluble fibrils in extracellular spaces. The most common type of familial amyloidosis is mediated by mutation of transthyretin, especially Val30Met. Symptoms and ejection fraction decrease may occur in cardiac amyloidosis only in case of poor prognosis. Myocardial strain detected by two-dimensional speckle tracking echocardiography can indicate changes in myocardial function at early stages of the disease.To determine the accuracy of left ventricular longitudinal strain by two-dimensional speckle tracking echocardiography in patients with familial amyloidosis caused by Val30Met transthyretin mutation.Eighteen consecutive patients, carriers of transthyretin mutation, were evaluated by two-dimensional speckle tracking echocardiography, by which myocardial strain curves were obtained, following the American Society of Echocardiography recommendations.Patients were divided into three groups: 1- Val30Met with cardiac amyloidosis; 2-Val30Met with extracardiac amyloidosis; 3 - Val30Met without evidence of disease. As the three groups were compared by the Mann-Whitney test, we found a statistically significant difference between groups 1 and 2 in the mean longitudinal tension (p=0.01), mean basal longitudinal strain (p=0.014); in mean longitudinal tension and mean longitudinal strain between groups 1 and 3 (p=0.005); and in the ratio of longitudinal strain of apical septum segment to longitudinal strain of basal septum (p=0.041) between groups 2 and 3.Left ventricular longitudinal strain detected by two-dimensional speckle tracking echocardiography is able to diagnose left ventricular dysfunction in early stages of familial amyloidosis caused by transthyretin Val30Met mutation.

Keywords

Adult, Cardiomyopathy, Dilated, Heart Ventricles, Ecocardiografia / métodos, Cardiomyopathy, Restrictive / complications, Prealbumin / analysis, Statistics, Nonparametric, Amiloidose Familiar / complicações, Amyloidosis, Familial / complications, Ventricular Dysfunction, Left, Reference Values, Diagnóstico por Imagem, Diseases of the circulatory (Cardiovascular) system, Humans, Prealbumin, Amyloid Neuropathies, Familial, Reproducibility of Results, Stroke Volume, Original Articles, Pré-Albumina / análise, Cardiomiopatia Restritiva / complicações, Cross-Sectional Studies, Echocardiography, RC666-701, Case-Control Studies, Diagnostic Imaging, Echocardiography / methods

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
2
Average
Average
Average
Green
gold