Audio Summary

doi : 10.1016/S0735-1097(25)06295-3

Volume 85, Issue 20, 27 May 2025, Page e177

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Contents

doi : 10.1016/S0735-1097(25)06297-7

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The Evolving Therapeutic Paradigm for Cardiac Amyloidosis

doi : 10.1016/j.jacc.2025.04.016

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Early Increase in Serum Transthyretin by Acoramidis Independently Predicts Improved Survival in TTR Amyloid Cardiomyopathy

doi : 10.1016/j.jacc.2025.03.542

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Serum Transthyretin as a Biomarker of Treatment Response in ATTR Cardiomyopathy

doi : 10.1016/j.jacc.2025.04.014

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Impact of Heart Failure Severity on Vutrisiran Efficacy in Transthyretin Amyloidosis With Cardiomyopathy

doi : 10.1016/j.jacc.2025.03.477

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Silence Disease Progression With Early Treatment of ATTR-CM

doi : 10.1016/j.jacc.2025.03.520

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Impact of Vutrisiran on Functional Capacity and Quality of Life in Transthyretin Amyloidosis With Cardiomyopathy

doi : 10.1016/j.jacc.2025.03.454

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Impact of Vutrisiran on Functional Capacity and Quality of Life in ATTR Cardiomyopathy: HELIOS-B Analysis

doi : 10.1016/j.jacc.2025.03.537

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Vutrisiran Improves Survival and Reduces Cardiovascular Events in ATTR Amyloid Cardiomyopathy: HELIOS-B

doi : 10.1016/j.jacc.2025.04.008

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Transthyretin Gene Silencing in Amyloid Transthyretin Cardiomyopathy: A Novel Treatment Delivers New Dilemmas

doi : 10.1016/j.jacc.2025.04.015

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Amara Yad Image: Left Anterior Oblique View of the Heart Showing Septal Perforators

doi : 10.1016/j.jacc.2025.04.012

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