Efficacy and Safety of Oral Chelators in Treatment of Patients With Wilson Disease

被引:158
作者
Weiss, Karl Heinz [1 ]
Thurik, Florentine [3 ]
Gotthardt, Daniel Nils [1 ]
Schaefer, Mark [1 ]
Teufel, Ulrike [2 ]
Wiegand, Franziska [1 ]
Merle, Uta [1 ]
Ferenci-Foerster, Daniela [4 ]
Maieron, Andreas [5 ]
Stauber, Rudolf [6 ]
Zoller, Heinz [7 ]
Schmidt, Hartmut H. [8 ]
Reuner, Ulrike [9 ]
Hefter, Harald [10 ]
Trocello, Jean Marc [11 ]
Houwen, Roderick H. J.
Ferenci, Peter [4 ]
Stremmel, Wolfgang [1 ]
机构
[1] Univ Heidelberg Hosp, Dept Gastroenterol, D-69120 Heidelberg, Germany
[2] Univ Heidelberg Hosp, Dept Pediat, D-69120 Heidelberg, Germany
[3] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Utrecht, Netherlands
[4] Univ Hosp Vienna, Dept Gastroenterol, Vienna, Austria
[5] Krankenhaus Elisabethinnen, Dept Gastroenterol, Linz, Austria
[6] Med Univ Graz, Div Gastroenterol & Hepatol, Dept Internal Med, Graz, Austria
[7] Univ Innsbruck Hosp, Dept Gastroenterol, A-6020 Innsbruck, Austria
[8] Muenster Univ Clin, Clin Transplantat Med, Munster, Germany
[9] Univ Hosp Dresden, Dept Neurol, Dresden, Germany
[10] Univ Hosp Duesseldorf, Dept Neurol, Dusseldorf, Germany
[11] Hosp Lariboisiere, Dept Neurol, Paris, France
关键词
ATP7B; Metabolic Disorder; Wilsons disease; Wilson's Disease; TRIETHYLENE TETRAMINE DIHYDROCHLORIDE; NEUROLOGICALLY AFFECTED PATIENTS; LONG-TERM TREATMENT; AMMONIUM TETRATHIOMOLYBDATE; PENICILLAMINE THERAPY; INITIAL THERAPY; ZINC THERAPY; LIVER-TRANSPLANTATION; FOLLOW-UP; EXPERIENCE;
D O I
10.1016/j.cgh.2013.03.012
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Wilson disease is a genetic copper storage disorder that causes hepatic and neurologic symptoms. Chelating agents (D-penicillamine, trientine) are used as first-line therapies for symptomatic patients, but there are few data from large cohorts. We assessed the safety of D-penicillamine and trientine therapy and outcomes of patients with Wilson disease. METHODS: We performed a retrospective analysis of data on 380 patients with Wilson disease from tertiary care centers in Germany and Austria, and 25 additional patients from the EUROWILSON registry. Chelator-based treatment regimens were analyzed for their effect on neurologic and hepatic symptoms and for adverse events that led to discontinuation of therapy (Kaplan-Meier estimation; data were collected for a mean of 13.3 y after therapy began). RESULTS: Changes in medication were common, resulting in analysis of 471 chelator monotherapies (326 patients receiving D-penicillamine and 141 receiving trientine). Nine of 326 patients treated with D-penicillamine and 3 of 141 patients given trientine underwent liver transplantation. Adverse events leading to discontinuation of treatment were more frequent among those receiving D-penicillamine than trientine (P = .039). Forty-eight months after therapy, hepatic deterioration was reported in only 4 of 333 patients treated initially with a chelating agent. Hepatic improvements were observed in more than 90%, and neurologic improvements were observed in more than 55%, of therapy-naive patients, and values did not differ significantly between treatments. However, neurologic deterioration was observed less frequently in patients given D-penicillamine first (6 of 295) than those given trientine first (4 of 38; P = .018). CONCLUSIONS: Chelating agents are effective therapies for most patients with Wilson disease; D-penicillamine and trientine produce comparable outcomes, although D-penicillamine had a higher rate of adverse events. Few patients receiving chelation therapy had neurologic deterioration, which occurred more frequently in patients who received trientine.
引用
收藏
页码:1028 / +
页数:10
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