Serum Transthyretin as a Biomarker of Treatment Response in ATTR Cardiomyopathy
- PMID: 40398972
- PMCID: PMC12163915
- DOI: 10.1016/j.jacc.2025.04.014
Serum Transthyretin as a Biomarker of Treatment Response in ATTR Cardiomyopathy
Keywords: ATTR-CM; TTR stabilization; acoramidis; all-cause mortality; serum TTR; transthyretin.
Conflict of interest statement
Funding Support and Author Disclosures Dr Regan has received research support from the National Heart, Lung, and Blood Institute (K38, HL175026). Dr Khouri has acted as consultant, advisor, or speaker for Alnylam Pharmaceuticals, AstraZeneca, BridgeBio Pharma, and Pfizer. Dr Ruberg has received research support from the National Heart, Lung, and Blood Institute (R01 HL139671), Anumana, Pfizer, and TriNetX; and has consulted for Attralus and AstraZeneca. Dr Selvaraj has received research support from the National Heart, Lung, and Blood Institute (K23 HL161348), American Heart Association (935275), American Academy of CME, and the Foundation for Sarcoidosis Research; and has consulted for AstraZeneca and BridgeBio. Dr Kittleson has reported that she has no relationships relevant to the contents of this paper to disclose.
References
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- Maurer MS, Judge DP, Gillmore JD, et al. Early increase in serum transthyretin by acoramidis independently predicts improved survival in TTR amyloid cardiomyopathy. J Am Coll Cardiol. 2025;85(20):1911–1923. - PubMed
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- Judge DP, Heitner SB, Falk RH, et al. Transthyretin stabilization by AG10 in symptomatic transthyretin amyloid cardiomyopathy. J Am Coll Cardiol. 2019;74:285–295. - PubMed
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