Wang Zuowei, Li Zezhi, Gao Keming, Fang Yiru
Division of Mood Disorders, Hongkou District Mental Health Center of Shanghai, Shanghai, 200083, P. R. China.
Division of Mood Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200030, P. R. China.
BMC Psychiatry. 2014 Dec 24;14:366. doi: 10.1186/s12888-014-0366-9.
In view of previous conflicting findings, this meta-analysis was performed to comprehensively determine the overall strength of associations between brain-derived neurotrophic factor (BDNF) genetic polymorphism Val66Met and susceptibility to bipolar disorders (BPD).
Literatures published and cited in Pubmed and Wanfang Data was searched with terms of 'Val66Met', 'G196A', 'rs6265', 'BDNF', 'association', and 'bipolar disorder' up to March 2014. All original case-control association studies were meta-analyzed with a pooled OR to estimate the risk and 95% confidence interval (CI) to reflect the magnitude of variance.
Twenty-one case-control association studies met our criteria for the meta-analysis. Overall, there was no significant difference in allelic distribution of Val66Met polymorphism between patients and controls with a pooled OR = 1.03 (95% CI 0.98, 1.08) although there was a trend towards association between Val66Met polymorphism and BPD in Caucasians with an OR of 1.08 (95% CI 1.00, 1.16). However, subgroup analyses showed that there was a significant association of Val allele with decreased disease susceptibility for bipolar disorder type II with a pooled OR of 0.88 (95% CI 0.78, 0.99).
There is no compelling evidence to supportVal66Met polymorphism in BDNF gene playing an important role in the susceptibility to BPD across different ethnicities.
鉴于之前相互矛盾的研究结果,进行了这项荟萃分析,以全面确定脑源性神经营养因子(BDNF)基因多态性Val66Met与双相情感障碍(BPD)易感性之间关联的总体强度。
在PubMed和万方数据中检索截至2014年3月发表和引用的文献,检索词为“Val66Met”、“G196A”、“rs6265”、“BDNF”、“关联”和“双相情感障碍”。所有原始病例对照关联研究均采用合并比值比(OR)进行荟萃分析,以估计风险,并采用95%置信区间(CI)反映变异程度。
21项病例对照关联研究符合我们的荟萃分析标准。总体而言,患者与对照之间Val66Met多态性的等位基因分布无显著差异,合并OR = 1.03(95%CI 0.98,1.08),尽管在白种人中Val66Met多态性与BPD之间存在关联趋势,OR为1.08(95%CI 1.00,1.16)。然而,亚组分析显示,Val等位基因与II型双相情感障碍疾病易感性降低存在显著关联,合并OR为0.88(95%CI 0.78,0.99)。
没有确凿证据支持BDNF基因中的Val66Met多态性在不同种族的BPD易感性中起重要作用。