Exercise limitations in amyloid cardiomyopathy assessed by cardiopulmonary exercise testing-A multicentre study.

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Tác giả: Piergiuseppe Agostoni, Chiara Arzilli, Roza Badr Eslam, Andrea Baggiano, Alice Bonomi, Christophe D J Capelle, Nicolò Capra, Vincenzo Castiglione, Fabrizio Celeste, Mauro Contini, Alberico Del Torto, Michele Emdin, Nikita Ermolaev, Iacopo Fabiani, Emiliano Fiori, Andreas Kammerlander, Christina Kronberger, Damiano Magrì, Beatrice Musumeci, Claudio Passino, René Rettl, Elisabetta Salvioni, Susanna Sciomer, Giacomo Tini, Giuseppe Vergaro, Robin Willixhofer

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: England : ESC heart failure , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 715658

AIMS: Amyloid cardiomyopathy is caused by the deposition of light chain (AL) or transthyretin amyloid (ATTR) fibrils, that leads to a restrictive cardiomyopathy, often resulting in heart failure (HF) with preserved or reduced ejection fraction. This study aimed to determine whether cardiac output reduction or ventilation inefficiency plays a predominant role in limiting exercise in patients with amyloid cardiomyopathy. METHODS: We conducted a multicentre prospective study in patients with AL or ATTR cardiomyopathy who underwent cardiopulmonary exercise testing across four centres. Patients were compared with a propensity-score matched HF cohort based on age, gender, left ventricular ejection fraction (LVEF), and peak oxygen consumption (VO RESULTS: Data from 267 amyloid patients aged 77 (72, 81) years, 86% male, with a median N-terminal pro B-type natriuretic peptide (NT-proBNP) of 2187 (1140, 4383) ng/L, exercise parameters of peak VO CONCLUSIONS: A higher VE/VCO
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