Lazary Judit, Lazary Aron, Gonda Xenia, Benko Anita, Molnar Eszter, Juhasz Gabriella, Bagdy Gyorgy
Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Biol Psychiatry. 2008 Sep 15;64(6):498-504. doi: 10.1016/j.biopsych.2008.03.030. Epub 2008 May 16.
Since the first report of the significant gene-environment interaction (G x E) in depression published by Caspi et al., the literature is considerably contradictory in this field. To clarify this question, we analyzed the interaction between the serotonin transporter gene (SLC6A4) and threatening life events (TLE) on Zung Self-Rating Depression Score (ZSDS).
Five markers tagging the whole SLC6A4 gene (5-HTTLPR and 4 single nucleotide polymorphisms: rs2020942, rs140700, rs3798908, rs1042173) were genotyped in 567 nonclinical individuals. Generalized linear models were used to analyze single marker associations, and likelihood ratio tests and score tests were used for haplotype analysis.
Haplotype analysis revealed a significant global effect of haplotypes on ZSDS score in high TLE subgroup (p = .008). Besides the 5-HTTLPR, rs140700 tagging the middle region of the gene had significant effects. Subjects carrying the A allele of rs140700 scored lower on ZSDS independently of 5-HTTLPR carrier status. Explained variances for depressive phenotype were 1%, 4%, and 6% when 5-HTTLPR, 5-HTTLPR x TLE and 5-HTTLPR x rs140700 x TLE were included in the model, respectively.
Our results demonstrate heterogeneity of individuals carrying S alleles of 5-HTTLPR in association with high TLE providing possible explanation for the inconsistency of previous studies. In addition to the promoter, the middle region of the SLC6A4 gene carries the G x G x E interaction for mood, and this new model provided a higher explained variance. We report the first evidence for the significant effects of haplotypes of the SLC6A4 gene and threatening life events on depressive phenotype.
自卡斯皮等人发表关于抑郁症中显著基因 - 环境相互作用(G×E)的首篇报告以来,该领域的文献存在相当大的矛盾之处。为了阐明这个问题,我们分析了血清素转运体基因(SLC6A4)与威胁生命事件(TLE)对zung自评抑郁量表评分(ZSDS)的相互作用。
对567名非临床个体进行基因分型,检测标记整个SLC6A4基因的5个标记(5 - HTTLPR和4个单核苷酸多态性:rs2020942、rs140700、rs3798908、rs1042173)。使用广义线性模型分析单个标记关联,并使用似然比检验和计分检验进行单倍型分析。
单倍型分析显示,在高TLE亚组中,单倍型对ZSDS评分有显著的总体影响(p = 0.008)。除了5 - HTTLPR,标记基因中部区域的rs140700也有显著影响。携带rs140700 A等位基因的受试者,无论其5 - HTTLPR载体状态如何,ZSDS评分都较低。当模型分别纳入5 - HTTLPR、5 - HTTLPR×TLE和5 - HTTLPR×rs140700×TLE时,抑郁表型的解释方差分别为1%、4%和6%。
我们的结果表明,携带5 - HTTLPR S等位基因且伴有高TLE的个体具有异质性,这为先前研究的不一致性提供了可能的解释。除启动子外,SLC6A4基因的中部区域存在基因 - 基因 - 环境(G×G×E)对情绪的相互作用,且这个新模型具有更高的解释方差。我们首次报告了SLC6A4基因单倍型和威胁生命事件对抑郁表型有显著影响的证据。