reviewCirculationJun 1, 2020BRONZE OA

Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association

Maurer (Germany)

PubMed
Indexed incrossrefpubmed

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
Citations per year

Authors

9

Topics & keywords

Keywords
  • Medicine
  • Cardiac amyloidosis
  • Transthyretin
  • Cardiomyopathy
  • Intensive care medicine
  • Heart failure
  • Internal medicine
  • Cardiology
UN Sustainable Development Goals
  • Good health and well-being
No related works found for this paper.