Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Ferenci, P; Steindl-Munda, P; Vogel, W; Jessner, W; Gschwantler, M; Stauber, R; Datz, C; Hackl, F; Wrba, F; Bauer, P; Lorenz, O.
Diagnostic value of quantitative hepatic copper determination in patients with Wilson's Disease.
CLIN GASTROENTEROL HEPATOL. 2005; 3(8): 811-818. Doi: 10.1053/S1542-3565(05)00181-3
Web of Science PubMed FullText FullText_MUG Google Scholar

 

Co-Autor*innen der Med Uni Graz
Stauber Rudolf
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
BACKGROUND & AIMS: A 5-fold increase of hepatic copper concentration is considered as the best available test for diagnosis of hepatic Wilson's disease (WD). However, the sensitivity and specificity of this test have never been fully investigated. METHODS: Copper content was measured by flame atomic absorption spectroscopy in 114 liver biopsies obtained at diagnosis of WD, in 219 patients with noncholestatic liver diseases (including 144 with chronic hepatitis C and 44 with nonalcoholic fatty liver disease), and in 26 without evidence of liver disease. RESULTS: Liver copper content was >250 microg/g in 95 WD patients (83.3%), between 50 and 250 microg/g in 15, and below 50 microg/g in 4. It did not correlate with age (r(2) = .003), the grade of fibrosis, or the presence of stainable copper. Liver copper content was >250 or between 50 and 250 microg/g in 3 (1.4%) and 20 (9.1%) of 219 patients with noncholestatic liver diseases, respectively. By lowering the cutoff from 250 to 75 microg/g, the sensitivity of liver copper content to diagnose WD increased from 83.3% (95% confidence interval, 75.2%-89.6%) to 96.5% (91.3%-99.1%), but the specificity decreased from 98.6% (96.0%-99.7%) to 95.4% (91.8%-97.8%). CONCLUSIONS: There is no gold standard for the diagnosis of WD. Liver copper content is a useful parameter, but a value below 250 microg/g does not exclude WD. Diagnosis requires the combination of a variety of clinical and biochemical tests.
Find related publications in this database (using NLM MeSH Indexing)
Adenosine Triphosphatases - genetics
Adolescent - genetics
Adult - genetics
Aged - genetics
Aged, 80 and over - genetics
Biopsy - genetics
Case-Control Studies - genetics
Copper - metabolism
DNA Mutational Analysis - metabolism
Female - metabolism
Genetic Screening - metabolism
Hepatolenticular Degeneration - diagnosis
Humans - diagnosis
Liver - metabolism
Male - metabolism
Middle Aged - metabolism
Mutation - metabolism
ROC Curve - metabolism
Sensitivity and Specificity - metabolism
Spectrophotometry, Atomic - metabolism

© Med Uni Graz Impressum