Diagnosing cardiac amyloidosis in every-day practice: A practical guide for the cardiologist.
99mTc-DPD, 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid
AA, amyloid A amyloidosis
AApoA-1, apolipoprotein A-1 amyloidosis
AL, light chain amyloidosis
ATTR, transthyretin amyloidosis
ATTRv, variant transthyretin amyloidosis
ATTRwt, wild type transthyretin amyloidosis
Amyloidosis
CA, cardiac amyloidosis
Cardiomyopathy
ECV, Extracellular volume
EMB, endomyocardial biopsy
Heart failure
LGE, late gadolinium enhancement
LV, left ventricular/ left ventricular
Light chains
MGUS, monoclonal gammopathy of undetermined significance
MRI, magnetic resonance imaging
NT-proBNP, N-terminal pro B-type natriuretic peptide
PET, positron-emission tomography
SPECT, single photon emission computed tomography
Transthyretin
Journal
International journal of cardiology. Heart & vasculature
ISSN: 2352-9067
Titre abrégé: Int J Cardiol Heart Vasc
Pays: Ireland
ID NLM: 101649525
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
11
01
2020
revised:
12
04
2020
accepted:
14
04
2020
entrez:
7
5
2020
pubmed:
7
5
2020
medline:
7
5
2020
Statut:
epublish
Résumé
Cardiac amyloidosis (CA) has emerged as a previously underestimated cause of heart failure and mortality. Underdiagnosis resulted mainly from unawareness of the true disease prevalence and the non-specific symptoms of the disease. CA results from extracellular deposition of misfolded protein fibrils, commonly derived from transthyretin (ATTR) or immunoglobulin light chains (AL). A significant proportion of older patients with heart failure and other extracardiac manifestations suffer from ATTR-CA, whereas AL-CA is still considered a rare disease. This article provides an overview of CA with a special focus on current and emerging diagnostic modalities. Furthermore, we provide a diagnostic algorithm for the evaluation of patients with suspected CA in every-day practice.
Identifiants
pubmed: 32373710
doi: 10.1016/j.ijcha.2020.100519
pii: S2352-9067(20)30017-8
pii: 100519
pmc: PMC7191222
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
100519Informations de copyright
© 2020 The Authors.
Déclaration de conflit d'intérêts
The authors have no conflicts of interest.
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