Department of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
J Neural Transm (Vienna). 2010 Mar;117(3):393-401. doi: 10.1007/s00702-009-0360-4. Epub 2009 Dec 24.
Alterations in brain-derived neurotrophic factor (BDNF)-signaling pathways may play an important role in the pathophysiology of major depressive disorder (MDD). Several lines of evidence have suggested that gene-gene interactions may confer susceptibility to MDD. The aim of this study was to analyze the single and combined effects of genes in the BDNF signal-transduction pathway on MDD in a Chinese population. We recruited 447 patients with MDD and 432 age- and gender-matched control subjects. Five SNPs in three BDNF signal-transduction pathway genes (BDNF, GSK3B and AKT1) were used in association analyses. An allelic association between the GSK3B SNP rs6782799 and MDD was found in our sample (allelic: chi(2) = 5.24, P = 0.022, corrected P = 0.107; genotypic: chi(2) = 5.55, P = 0.062) with an odds ratio (OR) of 1.25 (95% confidence interval (CI) 1.03-1.52). Further gene-gene interaction analyses showed a significant effect of a two-locus BDNF/GSK3B interaction with MDD (GSK3B rs6782799 and BDNF rs7124442) (corrected P = 0.011), and also for a three-locus interaction (GSK3B rs6782799, BDNF rs6265 and BDNF rs7124442) (corrected P = 0.019). Individuals carrying the combination of two risk alleles showed an OR value of 4.00 (95% CI 2.05-7.79), while those with the combination of three risk alleles gave the largest OR value of 4.46 (95% CI 2.15-9.24). Taken together, these findings support the assertion that the GSK3B gene is an important susceptibility factor for MDD in a Han Chinese population.
脑源性神经营养因子(BDNF)信号通路的改变可能在重度抑郁症(MDD)的病理生理学中发挥重要作用。有几条证据表明,基因-基因相互作用可能导致 MDD 的易感性。本研究旨在分析 BDNF 信号转导通路中基因的单核苷酸多态性(SNP)和联合作用对中国人群 MDD 的影响。我们招募了 447 例 MDD 患者和 432 名年龄和性别匹配的对照。在关联分析中使用了三个 BDNF 信号转导通路基因(BDNF、GSK3B 和 AKT1)中的 5 个 SNP。在我们的样本中发现 GSK3B SNP rs6782799 与 MDD 之间存在等位基因关联(等位基因:chi(2) = 5.24,P = 0.022,校正后 P = 0.107;基因型:chi(2) = 5.55,P = 0.062),比值比(OR)为 1.25(95%置信区间(CI)为 1.03-1.52)。进一步的基因-基因相互作用分析显示,BDNF/GSK3B 相互作用与 MDD 存在显著影响(GSK3B rs6782799 和 BDNF rs7124442)(校正后 P = 0.011),且三基因相互作用(GSK3B rs6782799、BDNF rs6265 和 BDNF rs7124442)也存在显著影响(校正后 P = 0.019)。携带两个风险等位基因组合的个体的 OR 值为 4.00(95% CI 2.05-7.79),而携带三个风险等位基因组合的个体的 OR 值最大,为 4.46(95% CI 2.15-9.24)。综上所述,这些发现支持 GSK3B 基因是汉族人群 MDD 的重要易感因素的观点。