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Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy.

Publication ,  Journal Article
García-Pavía, P; Witteles, RM; Damy, T; Fontana, M; Palladini, G; Tsujita, K; Grodin, JL; Khouri, MG; Malhotra, S; Singh, V; AbouEzzeddine, OF ...
Published in: JACC Heart Fail
January 2026

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.

Duke Scholars

Published In

JACC Heart Fail

DOI

EISSN

2213-1787

Publication Date

January 2026

Volume

14

Issue

1

Start / End Page

102766

Location

United States

Related Subject Headings

  • Prognosis
  • Humans
  • Disease Progression
  • Cardiomyopathies
  • Amyloid Neuropathies, Familial
  • 3201 Cardiovascular medicine and haematology
  • 1102 Cardiorespiratory Medicine and Haematology
 

Citation

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Chicago
ICMJE
MLA
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García-Pavía, P., Witteles, R. M., Damy, T., Fontana, M., Palladini, G., Tsujita, K., … Maurer, M. S. (2026). Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy. JACC Heart Fail, 14(1), 102766. https://doi.org/10.1016/j.jchf.2025.102766
García-Pavía, Pablo, Ronald M. Witteles, Thibaud Damy, Marianna Fontana, Giovanni Palladini, Kenichi Tsujita, Justin L. Grodin, et al. “Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy.JACC Heart Fail 14, no. 1 (January 2026): 102766. https://doi.org/10.1016/j.jchf.2025.102766.
García-Pavía P, Witteles RM, Damy T, Fontana M, Palladini G, Tsujita K, et al. Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy. JACC Heart Fail. 2026 Jan;14(1):102766.
García-Pavía, Pablo, et al. “Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy.JACC Heart Fail, vol. 14, no. 1, Jan. 2026, p. 102766. Pubmed, doi:10.1016/j.jchf.2025.102766.
García-Pavía P, Witteles RM, Damy T, Fontana M, Palladini G, Tsujita K, Grodin JL, Khouri MG, Malhotra S, Singh V, AbouEzzeddine OF, Vaishnav J, Hanna M, Maurer MS. Monitoring Disease Progression in Patients With Transthyretin Amyloid Cardiomyopathy. JACC Heart Fail. 2026 Jan;14(1):102766.
Journal cover image

Published In

JACC Heart Fail

DOI

EISSN

2213-1787

Publication Date

January 2026

Volume

14

Issue

1

Start / End Page

102766

Location

United States

Related Subject Headings

  • Prognosis
  • Humans
  • Disease Progression
  • Cardiomyopathies
  • Amyloid Neuropathies, Familial
  • 3201 Cardiovascular medicine and haematology
  • 1102 Cardiorespiratory Medicine and Haematology