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Cardiac and autonomic function in patients with Wilson’s disease

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...

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Autores principales: Quick, Silvio, Reuner, Ulrike, Weidauer, Marie, Hempel, Charlotte, Heidrich, Felix Martin, Mues, Christoph, Sveric, Krunoslav Michael, Ibrahim, Karim, Reichmann, Heinz, Linke, Axel, Speiser, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348666/
https://www.ncbi.nlm.nih.gov/pubmed/30691535
http://dx.doi.org/10.1186/s13023-019-1007-7
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author Quick, Silvio
Reuner, Ulrike
Weidauer, Marie
Hempel, Charlotte
Heidrich, Felix Martin
Mues, Christoph
Sveric, Krunoslav Michael
Ibrahim, Karim
Reichmann, Heinz
Linke, Axel
Speiser, Uwe
author_facet Quick, Silvio
Reuner, Ulrike
Weidauer, Marie
Hempel, Charlotte
Heidrich, Felix Martin
Mues, Christoph
Sveric, Krunoslav Michael
Ibrahim, Karim
Reichmann, Heinz
Linke, Axel
Speiser, Uwe
author_sort Quick, Silvio
collection PubMed
description 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 < 0.001 and 0.05; age 30–39, p < 0.01 and not significant (ns); age 40–49, p < 0,01 and 0.001; age 50–59, p = ns and < 0.001, age 60–70, p < 0.05 and ns). CONCLUSION: Our data demonstrate that cardiac involvement and autonomic dysfunction in WD is possible, however the underlying cause is still not known. We suggest that patients with signs and symptoms of structural heart disease should be examined by a cardiologist in addition to the interdisciplinary treatment team of WD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-019-1007-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-63486662019-01-31 Cardiac and autonomic function in patients with Wilson’s disease Quick, Silvio Reuner, Ulrike Weidauer, Marie Hempel, Charlotte Heidrich, Felix Martin Mues, Christoph Sveric, Krunoslav Michael Ibrahim, Karim Reichmann, Heinz Linke, Axel Speiser, Uwe Orphanet J Rare Dis Research 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 < 0.001 and 0.05; age 30–39, p < 0.01 and not significant (ns); age 40–49, p < 0,01 and 0.001; age 50–59, p = ns and < 0.001, age 60–70, p < 0.05 and ns). CONCLUSION: Our data demonstrate that cardiac involvement and autonomic dysfunction in WD is possible, however the underlying cause is still not known. We suggest that patients with signs and symptoms of structural heart disease should be examined by a cardiologist in addition to the interdisciplinary treatment team of WD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-019-1007-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-28 /pmc/articles/PMC6348666/ /pubmed/30691535 http://dx.doi.org/10.1186/s13023-019-1007-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Quick, Silvio
Reuner, Ulrike
Weidauer, Marie
Hempel, Charlotte
Heidrich, Felix Martin
Mues, Christoph
Sveric, Krunoslav Michael
Ibrahim, Karim
Reichmann, Heinz
Linke, Axel
Speiser, Uwe
Cardiac and autonomic function in patients with Wilson’s disease
title Cardiac and autonomic function in patients with Wilson’s disease
title_full Cardiac and autonomic function in patients with Wilson’s disease
title_fullStr Cardiac and autonomic function in patients with Wilson’s disease
title_full_unstemmed Cardiac and autonomic function in patients with Wilson’s disease
title_short Cardiac and autonomic function in patients with Wilson’s disease
title_sort cardiac and autonomic function in patients with wilson’s disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348666/
https://www.ncbi.nlm.nih.gov/pubmed/30691535
http://dx.doi.org/10.1186/s13023-019-1007-7
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