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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Overview publication
Title | Tafamidis in the Treatment of ATTR-related Cardiomyopathy: Indications and Grey Zones. |
Date | 2024-07-01 |
Issue name | Heart failure clinics |
Issue number | v20.3:333-341 |
DOI | 10.1016/j.hfc.2024.03.007 |
PubMed | 38844304 |
Authors | |
Keywords | ATTR, Amyloidoses, Cardiomyopathy, Tafamidis, Transthyretin, Treatment |
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