Exchangeable copper: a reflection of the neurological severity in Wilson's disease

被引:76
作者
Poujois, A. [1 ,2 ]
Trocello, J. -M. [1 ,2 ]
Djebrani-Oussedik, N. [1 ,3 ]
Poupon, J. [1 ,3 ]
Collet, C. [1 ,4 ]
Girardot-Tinant, N. [1 ,2 ]
Sobesky, R. [1 ,5 ]
Habes, D. [1 ,6 ]
Debray, D. [7 ]
Vanlemmens, C. [8 ]
Fluchere, F. [9 ]
Ory-Magne, F. [10 ]
Labreuche, J. [11 ]
Preda, C. [12 ]
Woimant, F. [1 ,2 ]
机构
[1] Lariboisiere Hosp, AP HP, Natl Reference Ctr Wilsons Dis, Paris, France
[2] Lariboisiere Hosp, AP HP, Dept Neurol, Paris, France
[3] Lariboisiere Hosp, AP HP, Toxicol Lab, Paris, France
[4] Lariboisiere Hosp, AP HP, Mol Biol & Biochem Dept, Paris, France
[5] Hop Paul Brousse, AP HP, DHU Hepatinov, Hepatobiliary Ctr, Villejuif, France
[6] Kremlin Bicetre Hosp, AP HP, Hepatol & Pediat Dept, Le Kremlin Bicetre, France
[7] Hop Necker Enfants Malad, AP HP, Hepatol & Pediat Dept, Paris, France
[8] CHU Besancon, Dept Gastroenterol & Hepatol, Besancon, France
[9] CHU Marseille, Dept Neurol, Marseille, France
[10] CHU Toulouse, Dept Neurol, Toulouse, France
[11] CHRU Lille, EA2694, Biostat Unit, Lille, France
[12] CNRS, UMR 8524, Math Lab, Lille, France
关键词
brain; copper chelators; exchangeable copper; free copper; liver; neurological disorders; prognosis; Wilson's disease; PENICILLAMINE; DIAGNOSIS; THERAPY; TRIENTINE; PLASMA; COHORT;
D O I
10.1111/ene.13171
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose: The severity of Wilson's disease (WD) is linked to free copper accumulating in the liver and brain. Exchangeable copper (CuEXC) is a new technique to determine plasmatic copper and is useful in the diagnosis of WD. It is hypothesized that it may also enable a good evaluation of extra-hepatic involvement and its severity. Methods: Forty-eight newly diagnosed WD patients were prospectively evaluated using hepatic, neurological, ophthalmological and brain magnetic resonance imaging (MRI) scores. Three phenotypic presentations were distinguished: pre-symptomatic, hepatic and extra-hepatic. CuEXC was determined in addition to standard copper assays before decoppering therapy. Correlations between biological parameters and the different scores were determined and compared in the hepatic and extra-hepatic groups. Results: Extra-hepatic patients had significantly higher CuEXC values than those with the hepatic form (P < 0.0001). The overall ability of CuEXC to separate the two forms was satisfactory, with an area under the curve of 0.883 (95% confidence interval 0.771-0.996) and an optimal threshold for extrahepatic diagnosis of 2.08 mu mol/l (sensitivity 85.7%; specificity 94.1%). In extra-hepatic patients, CuEXC was the only biological marker to be positively correlated with the Unified Wilson Disease Rating Score (r = 0.45, P = 0.016), the Kayser-Fleischer ring score (r = 0.46, P = 0.014) and the brain MRI score (r = 0.38, P = 0.048), but it was not correlated with the hepatic score. Conclusions: Exchangeable copper determination is useful when diagnosing WD as a value >2.08 mu mol/l is indicative of the severity of the extra-hepatic involvement. In the case of purely hepatic presentation, atypical or mild neurological signs, it should encourage physicians to search for lesions in the brain and eyes.
引用
收藏
页码:154 / 160
页数:7
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