Chen Dingbang, Zhou Xiangxue, Hou Haiman, Feng Li, Liu JunXiu, Liang Yinyin, Lin Xiaopu, Zhang Jiwei, Wu Chao, Liang Xiuling, Pei Zhong, Li Xunhua
Department of Neurology, National Key Clinical Department and Key Discipline of Neurology, Guangdong Key Laboratory for Diagnosis and Treatment of Major Neurological Disease, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Department of Neurology, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, China.
Ther Adv Neurol Disord. 2016 Jul;9(4):310-6. doi: 10.1177/1756285616641598. Epub 2016 Apr 7.
There are limited pharmacological treatments for patients with neurological Wilson's disease (WD) and a history of copper-chelating treatment failure.
We retrospectively evaluated the clinical records of 38 patients with WD who were treated with sodium dimercaptopropanesulfonate (DMPS) and zinc (group 1) or zinc alone (group 2). All patients had a history of neurological deterioration during their previous treatment with D-penicillamine (DPA).
Twenty-one patients were treated with intravenous DMPS for 4 weeks, followed by zinc gluconate for 6 months, and the treatment protocol was repeated twice. Relative to the baseline, repeated DMPS therapy and zinc maintenance therapy decreased neurological scores continuously (p < 0.01). Sixteen patients (76.2%) demonstrated neurological improvements after 1 year of therapy and four patients (19.0%) exhibited neurological deterioration at the follow-up session. In addition, 17 patients were treated with zinc monotherapy for 12 months. Two patients (11.8%) demonstrated neurological improvements and five patients (29.4%) exhibited neurological deterioration. Compared with the patients in group 2, a greater improvement ratio (p < 0.01) and lower deterioration ratio (p < 0.01) were observed in the patients in group 1 after 1 year of therapy.
Our findings indicate that the safety and efficacy of combined treatment of DMPS and zinc is superior to those of zinc monotherapy in patients with neurological WD with a history of DPA treatment failure.
对于患有神经型威尔逊病(WD)且有铜螯合治疗失败史的患者,可用的药物治疗有限。
我们回顾性评估了38例接受二巯丙磺酸钠(DMPS)和锌治疗(第1组)或仅接受锌治疗(第2组)的WD患者的临床记录。所有患者在先前使用青霉胺(DPA)治疗期间均有神经功能恶化史。
21例患者接受静脉注射DMPS治疗4周,随后接受葡萄糖酸锌治疗6个月,该治疗方案重复两次。与基线相比,重复DMPS治疗和锌维持治疗使神经评分持续下降(p<0.01)。16例患者(76.2%)在治疗1年后神经功能有所改善,4例患者(19.0%)在随访时神经功能恶化。此外,17例患者接受了12个月的锌单一疗法治疗。2例患者(11.8%)神经功能有所改善,5例患者(29.4%)神经功能恶化。与第2组患者相比,第1组患者在治疗1年后的改善率更高(p<0.01),恶化率更低(p<0.01)。
我们的研究结果表明,对于有DPA治疗失败史的神经型WD患者,DMPS和锌联合治疗的安全性和有效性优于锌单一疗法。