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Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid

Beinhardt, S; Leiss, W; Stättermayer, AF; Graziadei, I; Zoller, H; Stauber, R; Maieron, A; Datz, C; Steindl-Munda, P; Hofer, H; Vogel, W; Trauner, M; Ferenci, P.
Long-term outcomes of patients with Wilson disease in a large Austrian cohort.
Clin Gastroenterol Hepatol. 2014; 12(4):683-689
Web of Science PubMed FullText FullText_MUG


Autor/innen der Med Uni Graz:
Stauber Rudolf
Trauner Michael

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Plum Analytics:
Wilson disease is an autosomal recessive disorder that affects copper metabolism, leading to copper accumulation in liver, central nervous system, and kidneys. There are few data on long-term outcomes and survival from large cohorts; we studied these features in a well-characterized Austrian cohort of patients with Wilson disease. We analyzed data from 229 patients diagnosed with Wilson disease from 1961 through 2013; 175 regularly attended a Wilson disease outpatient clinic and/or their physicians were contacted for information on disease and treatment status and outcomes. For 53 patients lost during the follow-up period, those that died and reasons for their death were identified from the Austrian death registry. The mean observation period was 14.8 ± 11.4 years (range, 0.5-52.0 years), resulting in 3116 patient-years. Of the patients, 61% presented with hepatic disease, 27% with neurologic symptoms, and 10% were diagnosed by family screening at presymptomatic stages. Patients with a hepatic presentation were diagnosed younger (21.2 ± 12.0 years) than patients with neurologic disease (28.8 ± 12.0; P < .001). In 2% of patients, neither symptoms nor onset of symptoms could be determined with certainty. Most patients stabilized (35%) or improved on chelation therapy (26% fully recovered, 24% improved), but 15% deteriorated; 8% required a liver transplant, and 7.4% died within the observation period (71% of deaths were related to Wilson disease). A lower proportion of patients with Wilson disease survived for 20 years (92%) than healthy Austrians (97%), adjusted for age and sex (P = .03). Cirrhosis at diagnosis was the best predictor of death (odds ratio, 6.8; 95% confidence interval, 1.5-31.03; P = .013) and need for a liver transplant (odds ratio, 07; 95% confidence interval, 0.016-0.307; P < .001). Only 84% of patients with cirrhosis survived 20 years after diagnosis (compared with healthy Austrians, P =.008). Overall, patients who receive adequate care for Wilson disease have a good long-term prognosis. However, cirrhosis increases the risk of death and liver disease. Early diagnosis, at a precirrhotic stage, might increase survival times and reduce the need for a liver transplant. Copyright © 2014 AGA Institute. Published by Elsevier Inc. All rights reserved.
Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Adult -
Adult - epidemiology
Child -
Child, Preschool -
Female -
Hepatolenticular Degeneration - epidemiology Hepatolenticular Degeneration - mortality
Humans -
Male -
Middle Aged -
Prognosis -
Retrospective Studies -
Survival Analysis -
Treatment Outcome -
Young Adult -

Find related publications in this database (Keywords)
Genetic Liver Disease
Inherited Liver Disease
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