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强迫症患者认知功能与儿茶酚氧位甲基转移酶基因多态性的关系 被引量:3

Relationship Between Cognitive Function and COMT Gene Polymorphism in OCD Patients
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摘要 目的探讨强迫症(OCD)患者认知功能与儿茶酚氧位甲基转移酶(COMT)基因多态性之间的关联性。方法对88名OCD患者应用PCR及RFLP技术检测COMT基因的多态性;并采用威斯康星卡片分类测试(WCST)、连线试验A和B、韦氏积木拼图子测试测评所有患者的执行功能、注意和操作智商。结果 OCD患者COMT基因多态性频率分布符合Hardy-Weinberg平衡法则(χ2=0.00,P=0.99);患者的WCST测试,连线测试A和B以及韦氏积木拼图测试在G/G、G/A、A/A三个基因型组间均无显著性差异(P>0.05)。结论 OCD患者的执行功能、注意和操作智商可能并不会受COMT基因多态性的影响。 Objective To explore the association between cognition and catechol-O-methyl transferase (COMT) gene polymorphism in patients with OCD. Methods 88 OCD patients' COMT gene polymorphism were tested by PCR-RFLP technique; meanwhile, Wisconsin card sorting test (WCST), trail making test A and B (TMT A and B) and Wechsler intelligence scales: block design subtest (WISC: BD) were employed to assess executive function, attention and performance intelligence quotient. Results The distribution of COMT genotypic frequency accorded with the Hardy-Weinberg equilibrium (χ2 = 0.00, P = 0.99). However, there was no positive association between the COMT gene polymorphism and the tests of WSCT, TMT A and B, WISC (P 〉0.05). Conclusions The executive function, attention and performance intelligence quotient may not be influenced by the COMT gene polymorphism in OCD patients.
出处 《临床医学工程》 2013年第8期933-934,共2页 Clinical Medicine & Engineering
基金 广东省自然科学基金资助项目(项目编号:6012929)
关键词 强迫症 认知功能 儿茶酚氧位甲基转移酶 基因 Obsessive-compulsive disorder Cognitive function Catechol-O-methyl transferase Gene
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