Tafamidis in the Treatment of ATTR-related Cardiomyopathy: Indications and Grey Zones.

Transthyretin amyloid cardiomyopathy (ATTR-CM) is caused by the myocardial extracellular deposition of amyloid fibrils formed from the dissociation of TTR tetramer into monomers. The rate-limiting step in TTR amyloidogenesis is the dissociation of the TTR tetramer into monomers: Tafamidis is an effective TTR-stabilizer in its native homotetrameric structure. Tafamidis is a safe and effective drug in reducing symptoms, hospitalization and mortality in accurately selected patients affected by hereditary and wild-type transthyretin amyloid cardiomyopathy.

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TitleTafamidis in the Treatment of ATTR-related Cardiomyopathy: Indications and Grey Zones.
Date2024-07-01
Issue nameHeart failure clinics
Issue numberv20.3:333-341
DOI10.1016/j.hfc.2024.03.007
PubMed38844304
AuthorsCapovilla TM, Lalario A, Rossi M, Porcari A, Aimo A, Limongelli G, Emdin M, Merlo M & Sinagra G
KeywordsATTR, Amyloidoses, Cardiomyopathy, Tafamidis, Transthyretin, Treatment
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