Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy

Recognizing the lack of disease monitoring recommendations in transthyretin amyloid cardiomyopathy (ATTR-CM), international experts convened in 2021 to propose criteria for monitoring disease progression. Data have since been published demonstrating the prognostic value of certain parameters in ATTR-CM. Additionally, increased awareness and advances in diagnostic methods have led to a shift toward diagnosis at earlier stages of disease. In light of these developments, international experts with experience in treating ATTR-CM reviewed the available data, considered the feasibility of implementing evaluations in clinical practice, and proposed an update to the 2021 criteria. The criteria, with meaningful thresholds and monitoring frequency recommendations, are specifically designed to measure disease progression in patients with ATTR-CM, rather than to define progression of amyloid deposition. It remains unknown whether disease progression is an indicator for modifications to ATTR-CM treatment. Future studies should investigate whether changes in ATTR-CM disease-modifying treatment improve outcomes in patients demonstrating disease progression.

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Publication Details

Journal
JACC Heart Failure
Published
2025-12-01
DOI
https://doi.org/10.1016/j.jchf.2025.102766
Citations
1
Primary Topic
Amyloidosis: Diagnosis, Treatment, Outcomes
Type
article
Field-Weighted Citation Impact
0.81
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article

Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy

Joban Vaishnav, Michael G. Hanna, Ronald Witteles, Kenichi Tsujita et al.
1 citations
JACC Heart Failure
Amyloidosis: Diagnosis, Treatment, Outcomes
0.81
article

Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy

Joban Vaishnav, Michael G. Hanna, Ronald Witteles, Kenichi Tsujita, Michel G. Khouri, Justin L. Grodin, Matthew J. Maurer, Saurabh Malhotra, Giovanni O. Palladini, Omar F. AbouEzzeddine, Marianna Fontana, Vasvi Singh, Thibaud Damy, Pablo García-Pavía
article en
1 citations

Abstract

Recognizing the lack of disease monitoring recommendations in transthyretin amyloid cardiomyopathy (ATTR-CM), international experts convened in 2021 to propose criteria for monitoring disease progression. Data have since been published demonstrating the prognostic value of certain parameters in ATTR-CM. Additionally, increased awareness and advances in diagnostic methods have led to a shift toward diagnosis at earlier stages of disease. In light of these developments, international experts with experience in treating ATTR-CM reviewed the available data, considered the feasibility of implementing evaluations in clinical practice, and proposed an update to the 2021 criteria. The criteria, with meaningful thresholds and monitoring frequency recommendations, are specifically designed to measure disease progression in patients with ATTR-CM, rather than to define progression of amyloid deposition. It remains unknown whether disease progression is an indicator for modifications to ATTR-CM treatment. Future studies should investigate whether changes in ATTR-CM disease-modifying treatment improve outcomes in patients demonstrating disease progression.

JACC Heart FailureVol. 14(1)
Rush University Medical Center (US), Cleveland Clinic (US), Mayo Clinic (US), Johns Hopkins University (US), Inserm (FR), Duke University (US), Université Paris-Est Créteil (FR), University of Pavia (IT), Columbia University Irving Medical Center (US), Assistance Publique – Hôpitaux de Paris (FR), Hospital Universitario Puerta de Hierro Majadahonda (ES), Hôpitaux Universitaires Henri-Mondor (FR), Stanford Medicine (US), Mayo Clinic in Florida (US), Institut Mondor de Recherche Biomédicale (FR), Cook County Health and Hospitals System (US), The University of Texas Southwestern Medical Center (US), Kumamoto University (JP), Stanford University (US)
Openalex Percentile: Top 21%
Amyloidosis: Diagnosis, Treatment, Outcomes
0.81
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