Combining ECG and echocardiography to identify transthyretin cardiac amyloidosis in heart failureVisa övriga samt affilieringar
2021 (Engelska)Ingår i: Clinical Physiology and Functional Imaging, ISSN 1475-0961, E-ISSN 1475-097X, Vol. 41, nr 5, s. 408-416Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
AIMS/BACKGROUND: Transthyretin amyloid (ATTR) amyloidosis cardiomyopathy is an underdiagnosed, causatively treatable cause of heart failure. The aim of this study was to evaluate the efficacy of electrocardiography (ECG) and echocardiography on patients with increased interventricular septum diameter (IVSd) to identify ATTR cardiac amyloidosis (ATTR-CA) patients.
METHODS: We investigated 58 patients with heart failure and an IVSd >14mm. Included were 33 ATTR-CA patients and 25 controls that consisted of non-amyloidosis heart failure (HF) patients with negative 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid (DPD) scintigraphy. We used echocardiography including 2D speckle tracking strain and a 12-lead ECG to test the accuracy to differentiate the groups.
RESULTS: We found high diagnostic accuracy (98%) for differentiating ATTR-CA from HF controls using a combination of R amplitude in -aVR from ECG and relative wall thickness acquired from echocardiography. With this combined model (RWT/ R in -aVR), the sensitivity was 100% and specificity was 95% using a cut off value of 0.90. Furthermore, the area under the curve was 99% and the negative predictive value was 100%.
CONCLUSION: We found that a simple combination of ECG and echocardiographic parameters used in clinical settings was able to differentiate ATTR-CA from other etiologies of HF with increased interventricular septum thickness. The high sensitivity and negative predictive value render the algorithm useful for selection of patients for further diagnostic procedures for ATTR-CA.
Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2021. Vol. 41, nr 5, s. 408-416
Nyckelord [en]
Cardiac amyloidosis, ECG, Echocardiography, Heart failure, Transthyretin amyloidosis
Nationell ämneskategori
Kardiologi och kardiovaskulära sjukdomar
Identifikatorer
URN: urn:nbn:se:umu:diva-183897DOI: 10.1111/cpf.12715ISI: 000661468500001PubMedID: 34033209Scopus ID: 2-s2.0-85107933221OAI: oai:DiVA.org:umu-183897DiVA, id: diva2:1560060
Forskningsfinansiär
Hjärt-Lungfonden, 20160787Hjärt-Lungfonden, 20200160Vetenskapsrådet, 2019-013382021-06-032021-06-032025-02-10Bibliografiskt granskad