多巴胺D4受体基因启动子区多态性与慢性抽动障碍的关联研究(英文)  

Association between the polymorphism in the promoter region of dopamine D4 receptor gene and chronic tic disorder

作　　者：卢瑶[1] 麻宏伟[1] 郗春艳[1] 张莹[1] 王雁[1] 姚璐[1] 高建[1] 汪薇[1] 周末[1] 

机构地区：[1]中国医科大学实验技术中心,辽宁沈阳110001

出　　处：《中国当代儿科杂志》2006年第5期357-360,共4页Chinese Journal of Contemporary Pediatrics

基　　金：Supported by the National Natural Science Foundation of China (No. 30471842).

摘　　要：目的探讨多巴胺D4受体(DRD4)基因启动子区的3个功能多态性与慢性抽动障碍是否存在相关性。方法选取无亲缘关系的慢性抽动障碍患儿84例以及无亲缘关系的健康个体100例,后者作为对照组。提取静脉血白细胞基因组DNA,采用聚合酶链反应及等位基因特异性扩增技术检测DRD4基因启动子区-1240L/S,-616C/G和-521C/T3个功能位点的基因型。用SHEsis在线统计软件分析各位点等位基因、基因型、单倍型频率及其组间差异。结果DRD4基因-616C/G的等位基因频率及其基因型频率在慢性抽动障碍组显著高于正常对照组(χ2=8.419,P<0.01;χ2=7.860,P<0.05),DRD4基因-1240L/S,-616C/G和-521C/T组成的单倍型LCT的频率在慢性抽动障碍组显著高于正常对照组(χ2=6.371,P<0.05)。结论DRD4基因-616C/G的等位基因可能与慢性抽动障碍相关联,携带有DRD4基因-1240L/S,-616C/G和-521C/T组成的单倍型LCT的个体可能更易患慢性抽动障碍。Objective To study a possible association between the three functional polymorphisms in the promoter region of dopamine D4 receptor （ DRD4 ） gene and chronic tic disorder. Methods Genomic DNA was isolated from the venous blood leukocytes of 84 unrelated patients with chronic tic disorder （Study group） and 100 healthy unrelated individuals （Control group）. Polymorphlsms of DRD4, -1240L/S, -616C/G and -521C/T, were genotyped by the allelespecific primer （ASP） PCR. Genotype, allele and haplotype frequencies were analysed by SHEsis online. Results There were significant differences in both allele and genotype frequencies （ x^2 = 8. 419, P 〈 0. 01 ; x^2 = 7. 860, P 〈 0. 05 respectively） of DRD4-616C/G between the Study and the Control groups. Haplotypic frequencies of LCT （-1240L/S, -616C/G, -521C/T） in the Study group were noticeably higher than in the Control group （ x^2 = 6. 371, P 〈 0.05 ）. Conclusions There is an association between the DRD4-616C/G polymorphism and chronic tic disorder. The individuals with haplotype LCT （-1240L/S, -616C/G, -521C/T） are susceptible to this disorder.

关 键 词：慢性抽动障碍 多巴胺D4受体 聚合酶链反应 等位基因特异性扩增 单倍型 

分 类 号：R749.94[医药卫生—神经病学与精神病学]