Echocardiographic markers of cardiac amyloidosis in patients with heart failure and left ventricular hypertrophy

Cardiac amyloidosis (CA), following a non-invasive diagnosis, constitutes an increasingly prevalent heart failure (HF) etiology. This study aims to determine which echocardiography findings help to diagnose CA in patients with left ventricular hypertrophy (LVH) admitted for decompensated HF. The pre...

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Veröffentlicht in:Cardiology journal 2023-04, Vol.30 (2), p.266-275
Hauptverfasser: Melero Polo, Jorge, Roteta Unceta-Barrenechea, Ana, Revilla Martí, Pablo, Pérez-Palacios, Raquel, Gracia Gutiérrez, Anyuli, Bueno Juana, Esperanza, Andrés Gracia, Alejandro, Atienza Ayala, Saida, Aibar Arregui, Miguel Ángel
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container_end_page 275
container_issue 2
container_start_page 266
container_title Cardiology journal
container_volume 30
creator Melero Polo, Jorge
Roteta Unceta-Barrenechea, Ana
Revilla Martí, Pablo
Pérez-Palacios, Raquel
Gracia Gutiérrez, Anyuli
Bueno Juana, Esperanza
Andrés Gracia, Alejandro
Atienza Ayala, Saida
Aibar Arregui, Miguel Ángel
description Cardiac amyloidosis (CA), following a non-invasive diagnosis, constitutes an increasingly prevalent heart failure (HF) etiology. This study aims to determine which echocardiography findings help to diagnose CA in patients with left ventricular hypertrophy (LVH) admitted for decompensated HF. The present study is a retrospective observational study on a cohort of 85 LVH patients admitted for HF decompensation, in which 99mTc-DPD scanning was performed to rule out transthyretin CA. The echocardiographic findings obtained were compared between CA and non-CA groups. From a total number of 85 patients, 49 (57.6%) met the CA criteria and 36 (42.3%) were ruled out for the disease. Interventricular septum thickness (16 ± 3 mm vs. 14 ± 3 mm), left ventricular posterior wall thickness (14 ± 3 mm vs. 11 ± 2 mm), left ventricular mass (259 ± 76 g vs. 224 ± 53 g), left ventricular end-diastolic diameter (48 ± 7 mm vs. 53 ± 6 mm), left ventricular end-diastolic indexed volume (51 ± 18 cm3/m2 vs. 59 ± 16 cm3/m2), tricuspid annular plane systolic excursion (16 ± 5 mm vs. 20 ± 4 mm), right atrial area (27.4 ± 8.4 cm2 vs. 22.2 ± 5.7 cm2) and strain relative apical sparing (2.2 ± 0.9 vs. 1.03 ± 0.4; p = 0.04) were significantly associated with the diagnosis of CA. In patients with LVH admitted for HF decompensation, there are several echocardiographic features (LVH, reduced left ventricular cavity size, strain relative apical sparing, right atrial dilation, and altered right ventricular function) that are associated with the diagnosis of cardiac amyloidosis.
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subjects Amyloidosis
Amyloidosis - diagnosis
Amyloidosis - diagnostic imaging
Atrial Fibrillation - complications
Biopsy
Cardiology
Clinical Cardiology
Echocardiography
Heart failure
Heart Failure - diagnostic imaging
Heart Failure - etiology
Histology
Hospitalization
Humans
Hypertrophy, Left Ventricular - diagnostic imaging
Hypertrophy, Left Ventricular - etiology
Patients
Proteins
Ultrasonic imaging
title Echocardiographic markers of cardiac amyloidosis in patients with heart failure and left ventricular hypertrophy
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