Diagnosis and treatment of cardiac amyloidosis: position statement of the German Cardiac Society (DGK).
Amyloidosis
Endomyocardial biopsy
Magnetic resonance imaging
Myocardium
Scintigraphy
Journal
Clinical research in cardiology : official journal of the German Cardiac Society
ISSN: 1861-0692
Titre abrégé: Clin Res Cardiol
Pays: Germany
ID NLM: 101264123
Informations de publication
Date de publication:
Apr 2021
Apr 2021
Historique:
received:
30
10
2020
accepted:
21
12
2020
pubmed:
19
1
2021
medline:
20
11
2021
entrez:
18
1
2021
Statut:
ppublish
Résumé
Systemic forms of amyloidosis affecting the heart are mostly light-chain (AL) and transthyretin (ATTR) amyloidoses. The latter is caused by deposition of misfolded transthyretin, either in wild-type (ATTRwt) or mutant (ATTRv) conformation. For diagnostics, specific serum biomarkers and modern non-invasive imaging techniques, such as cardiovascular magnetic resonance imaging (CMR) and scintigraphic methods, are available today. These imaging techniques do not only complement conventional echocardiography, but also allow for accurate assessment of the extent of cardiac involvement, in addition to diagnosing cardiac amyloidosis. Endomyocardial biopsy still plays a major role in the histopathological diagnosis and subtyping of cardiac amyloidosis. The main objective of the diagnostic algorithm outlined in this position statement is to detect cardiac amyloidosis as reliably and early as possible, to accurately determine its extent, and to reliably identify the underlying subtype of amyloidosis, thereby enabling subsequent targeted treatment.
Identifiants
pubmed: 33459839
doi: 10.1007/s00392-020-01799-3
pii: 10.1007/s00392-020-01799-3
pmc: PMC8055575
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
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