多巴反应性肌张力障碍长期随访四例  

Long-term follow up of four patients with dopa-responsive dystonia

作　　者：利婧[1] 胡朝晖 喻长顺 操基清[1] 杨娟[1] 李亚勤[3] 詹益鑫 张成[1] 

机构地区：[1]中山大学附属第一医院神经科,广州510080 [2]金域医学检验中心有限公司 [3]中山大学干细胞与组织工程研究中心

出　　处：《中华神经科杂志》2013年第3期153-158,共6页Chinese Journal of Neurology

基　　金：国家自然科学基金/广东省联合基金重点资助项目（U1032004）;国家自然科学基金资助项目（30870851）;广东省计生委重点资助项目（201002）

摘　　要：目的总结多巴反应性肌张力障碍（dopa—responsive dystonia，DRD）的临床特点，探讨其治疗效果、随访结果及三磷酸鸟苷环化水解酶I（GCHI）基因、酪氨酸羟化酶（TH）基因突变情况。方法总结3个DRD家系共4例患者的临床资料，并对患者行GCHI基因及TH基因检测。结果4例患者均为女性，起病年龄为9—20（15．3±5．6）岁，均以双下肢僵硬、抖动起病，随病程进展其中3例出现双手抖动症状，1例患者出现全身扭转，1例患者合并有斜颈，4例患者均有晨轻暮重的表现。对4例患者进行小剂量左旋多巴治疗，随访半年至10年不等，患者均有持续、明显的疗效；且随时间延长所需剂量减少，无长期服用左旋多巴不良反应。对4例患者行GCHI基因全长外显子突变检测，1例患者呈GCHI基因杂合点突变C．607G〉A（p．Gly203Arg），1例患者为TH基因14号外显子复合杂合突变（p．Y447Ter及p．V468M），余患者未见GCHI基因及TH基因全长外显子点突变。结论长期随访发现小剂量左旋多巴对DRD患者具有显著而持久的疗效，且无明显副作用。GCHI基因及TH基因的检测可对DRD进行早期诊断，对于儿童期或青少年期起病的肌张力障碍患者，无论有无家族史，均需行小剂量多巴胺诊断眭治疗。Objective To investigate the clinical characteristics, treatment effect, long-term follow up results, gnanosine triphosphate （GTP） cyrclohydrolase I （ GCH I ） gene and tyrosine hydroxylase（TH） gene mutations in patients with dopa-responsive dystonia （ DRD ）. Methods The clinical features of 3 families with 4 affected members were analyzed and all of 4 patients were screened for mutations of the GCH I gene and TH gene with DNA sequences. Results Four patients were females, average age at onset was （15.3 ±5.6） years （range： from 9 to 20 years）. The initial symptoms were a gait disorder, stiffness or tremor of the lower limbs in all patients presented with diurnal fluctuation. As the increase of disease duration, bilateral hand tremor was found in three patients, systemic torsion was found in one patient and torticollis was found in one patient. All patients＇ symptoms were in complete remission after administration of low dose of levodopa. Four patients were followed up for 0. 5 to 10. 0 years, and all were still responsive to the levodopa treatment and effective dosage was decreased as the increase of the disease duration. No long- term side effects of levodopa had occurred after long-term treatment. One patient was found to have e. 607G 〉A （p. Gly203Arg） heterogenetic mutation in GCH I gene. Molecular analysis revealed a compound heterozygous mutation in the TH gene （p. Y447Ter and p. V468M） in one patient. No point mutations in both genes were found in other patients. Conclusions DRD patients have dramatic and sustained response to levodopa and no long-term side effects of levodopa after long-term treatment. The detection of GCH I and TH gene mutations is helpful in early diagnosis but the negative results could not exclude the diagnosis of DRD.

关 键 词：张力失调 左旋多巴 GTP环化水解酶 酪氨酸单氧化酶 随访研究 

分 类 号：R742.5[医药卫生—神经病学与精神病学]