| Literature DB >> 30767672 |
Massimiliano Lorenzini1,2, Perry M Elliott1.
Abstract
Transthyretin (TTR) related cardiomyopathy is an underdiagnosed cause of heart failure but is increasingly recognized in various settings - from patients admitted with heart failure to symptomatic aortic stenosis - and is rapidly becoming the most frequent form of systemic amyloidosis. Following the recent publication of the landmark ATTR-ACT trial that showed tafamidis to be the first treatment to improve survival in patients with TTR-related cardiac amyloidosis and heart failure, we reviewed the drug's rationale, characteristics and evidence supporting its use in TTR amyloidosis.Entities:
Keywords: amyloidosis; cardiomyopathy; tafamidis; transthyretin
Mesh:
Substances:
Year: 2019 PMID: 30767672 DOI: 10.2217/fca-2018-0078
Source DB: PubMed Journal: Future Cardiol ISSN: 1479-6678