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脑源性神经营养因子G196A基因多态性与抑郁症及认知功能的关系
引用本文:李含秋,王西林,张敏玲. 脑源性神经营养因子G196A基因多态性与抑郁症及认知功能的关系[J]. 新医学, 2012, 43(7): 466-470
作者姓名:李含秋  王西林  张敏玲
作者单位:广州市精神病医院精神科,510370
基金项目:2010年度广东省科技厅立项
摘    要:目的:探索脑源性神经营养因子(BDNF)G196A基因多态性与中国汉族人群抑郁症及其认知功能的关系。方法:采用病例对照研究方法,以153例抑郁症患者及180名正常对照人群为研究对象,采用PCR-RFLP技术检测BDNF G196A基因多态性,采用连线测验A和B、言语流畅性测验、威斯康辛卡片分类测验-改良版(M-WCST)、汉诺塔测验评定患者的认知功能。比较抑郁症患者与正常对照组BDNF基因型及等位基因频率的差异;比较携带不同等位基因或基因型的抑郁症患者认知功能的差异。结果:抑郁症患者BDNF基因A等位基因的频率(60.1%)高于对照组(52.2%),比较差异有统计学意义(P<0.05)。携带BDNF 196A等位基因的抑郁症患者的各项认知功能测验的成绩与没有携带A等位基因者比较差异无统计学意义(P>0.05)。按基因型分类比较抑郁症患者的认知功能,携带A/A型患者的WSCT分类数低于其它两种基因型携带者、WSCT持续错误数高于其他两种基因型携带者(P<0.05)。结论:BDNF 196A等位基因是抑郁症发病的危险因素,携带A/A基因型的抑郁症患者执行功能损害更严重。

关 键 词:抑郁症  脑源性神经营养因子  多态性  认知功能

The correlation between brain-derived neurotrophic factor gene G196A polymorphism and depression or cognitive function
LI Han-qiu , WANG Xi-lin , ZHANG Min-ling. The correlation between brain-derived neurotrophic factor gene G196A polymorphism and depression or cognitive function[J]. New Chinese Medicine, 2012, 43(7): 466-470
Authors:LI Han-qiu    WANG Xi-lin    ZHANG Min-ling
Affiliation:. Department of Psychiatric, Guangzhou Psychi- atric Hospital, Guangzhou 510370, China;
Abstract:Objective: To investigate the correlation between brain-derived neurotrophic factor (BDNF) G196A gene polymorphism and depression or cognitive function in Chinese Han population. Methods: Correlation study was performed in 153 patients with depression and 180 health individuals in Guangzhou, China. The G196A polymorphism of BDNF gene promoter was analyzed by polymerase chain reaction-restriction fragment length poly- morphism (PCR-RFLP). The cognitive function were assessed by Trail making test, verbal fluency, modified Wis- consin card sorting test (M-WCST), Tower of Hanoi test. Results: The frequency of BDNF gent 196A allele in depression group (60. 1% ) was significantly higher than that in control group (52. 2%, P 〈 0. 05 ). The results of cognitive function test in BDNF196A allele carriers were all not significantly different from those in non-A allele carriers (P 〉 0.05 ). The depressive patients with A / A genotype had significantly more categories in WSCT and less continuing errors than those in the other two genotype carriers (P 〈 0. 05). Conclusion: The A allele of BD-NF gene is a risk factor of depression. The depressive patients with A / A genotype performed worse executive func- tion.
Keywords:Depression  Brain-derived neurotrophic factor  Polymorphism  Cognitive function
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