Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association
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Abstract
Transthyretin amyloid cardiomyopathy (ATTR-CM) results in a restrictive cardiomyopathy caused by extracellular deposition of transthyretin, normally involved in the transportation of the hormone thyroxine and retinol-binding protein, in the myocardium. Enthusiasm about ATTR-CM has grown as a result of 3 simultaneous areas of advancement: Imaging techniques allow accurate noninvasive diagnosis of ATTR-CM without the need for confirmatory endomyocardial biopsies; observational studies indicate that the diagnosis of ATTR-CM may be underrecognized in a significant proportion of patients with heart failure; and on the basis of elucidation of the mechanisms of amyloid formation, therapies are now approved for…
Citation impact
705
total citations
- FWCI
- 29.59
- Percentile
- 100%
- References
- 64
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Authors
9Topics & keywords
Topics
Keywords
- Medicine
- Cardiac amyloidosis
- Transthyretin
- Cardiomyopathy
- Intensive care medicine
- Heart failure
- Internal medicine
- Cardiology
UN Sustainable Development Goals
- Good health and well-being
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