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Tafamidis in the Treatment of ATTR-related Cardiomyopathy: Indications and Grey Zones.
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- Additional Information
- Source:
Publisher: Elsevier/Saunders Country of Publication: United States NLM ID: 101231934 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1551-7136 (Print) Linking ISSN: 15517136 NLM ISO Abbreviation: Heart Fail Clin Subsets: MEDLINE
- Publication Information:
Original Publication: Philadelphia : Elsevier/Saunders, c2005-
- Subject Terms:
- Abstract:
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.
Competing Interests: Disclosure The authors have nothing to declare.
(Copyright © 2024 Elsevier Inc. All rights reserved.)
- Contributed Indexing:
Keywords: ATTR; Amyloidoses; Cardiomyopathy; Tafamidis; Transthyretin; Treatment
- Accession Number:
8FG9H9D31J (tafamidis)
0 (Benzoxazoles)
0 (Prealbumin)
- Subject Terms:
Amyloidosis, Hereditary, Transthyretin-Related
- Publication Date:
Date Created: 20240606 Date Completed: 20240606 Latest Revision: 20240606
- Publication Date:
20240607
- Accession Number:
10.1016/j.hfc.2024.03.007
- Accession Number:
38844304
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