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Cardiac and autonomic function in patients with Wilson’s disease

Authors :
Silvio Quick
Ulrike Reuner
Marie Weidauer
Charlotte Hempel
Felix Martin Heidrich
Christoph Mues
Krunoslav Michael Sveric
Karim Ibrahim
Heinz Reichmann
Axel Linke
Uwe Speiser
Source :
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-6 (2019)
Publication Year :
2019
Publisher :
BMC, 2019.

Abstract

Abstract Background The clinical effect of copper accumulation on the heart of patients suffering from Wilson’s disease (WD) is not completely understood. We aimed to determine if patients with WD show signs of cardiac involvement, structural heart disease or autonomic dysfunction. In this prospective trial, we studied 61 patients (mean age 44.3 ± 15.2 years, 51% males) with WD and compared them to 61 age- and gender-matched healthy controls. All subjects underwent clinical examination, blood tests, echocardiography and 24 h electrocardiographic (ECG) recording. Results Left- and right ventricular systolic function did not differ significantly between WD patients and controls. However, 5 of the 61 patients had a reduced left ventricular ejection fraction (LVEF). Furthermore, diastolic dysfunction was more prevalent in WD patients (9 of 61 vs. 0 of 61, p = 0.001). The severity of WD based on the Unified Wilson’s Disease Rating Scale was significantly correlated to NT-pro BNP (r = 0.34, P = 0.013). Patients with an exacerbation of WD in medical history had higher troponin levels compared to those without (11.3 ± 4.7 vs 4.6 ± 1.2). The autonomic function assessed by triangular index (TI) and SDNN-index was significantly reduced in WD patients compared to controls in most in almost every age category (p-value TI and SDNN: age 20–29, p

Details

Language :
English
ISSN :
17501172
Volume :
14
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.3d1ea94487674e77bf44198e9aae371d
Document Type :
article
Full Text :
https://doi.org/10.1186/s13023-019-1007-7