Bellivier Frank, Chaste Pauline, Malafosse Alain
Service de Psychiatrie Adulte (Pr Rouillon), Hôpital Henri Mondor et Albert Chenevier, Assistance Publique-Hôpitaux de Paris, Créteil, France.
Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):87-91. doi: 10.1002/ajmg.b.20015.
Genes encoding proteins involved in serotonergic metabolism are major candidates in association studies of suicidal behavior. The tryptophan hydroxylase (TPH) gene, which codes for the rate-limiting enzyme of serotonin biosynthesis, is a major candidate gene and has been extensively studied in association studies of suicidal behavior, providing conflicting results. It is difficult to interpret these conflicting results due to lack of power, ethnic heterogeneity, and variations in the sampling strategies (in particular for controls) and in the polymorphism of the TPH gene studied. Meta-analyses can improve the statistical power for the analysis of the effects of candidate vulnerability factors. The analysis of the sources of heterogeneity that contribute to these conflicting results is an important step in the interpretation of these conflicting association results and in the interpretation of the results of a meta-analysis. We selected all of the published association studies between the TPH gene polymorphism and suicidal behavior. Nine association studies between the A218C TPH polymorphism and suicidal behavior fulfilled the inclusion criteria. A significant association was observed between the A218C polymorphism and suicidal behavior using the fixed effect method (odds ratio (OR) = 1.62; 95% confidence interval (CI) = [1.26; 2.07]) and the random effect method (OR = 1.61; 95% CI = [1.11; 2.35]). The analysis of the sources of heterogeneity showed that two studies (one positive and one negative) significantly deviated from the calculated global effect. The meta-analysis performed after removing those two studies also revealed a significant association between the TPH A218C polymorphism and suicidal behavior. Both analyses suggested that the A allele has a dose-dependent effect on the risk of suicidal behavior.
编码参与血清素能代谢的蛋白质的基因是自杀行为关联研究中的主要候选基因。色氨酸羟化酶(TPH)基因编码血清素生物合成的限速酶,是一个主要的候选基因,并且在自杀行为的关联研究中已得到广泛研究,但结果相互矛盾。由于缺乏统计学效力、种族异质性以及抽样策略(特别是对照组)和所研究的TPH基因多态性的差异,难以解释这些相互矛盾的结果。荟萃分析可以提高分析候选易感性因素作用的统计学效力。分析导致这些相互矛盾结果的异质性来源是解释这些相互矛盾的关联结果以及解释荟萃分析结果的重要一步。我们筛选了所有已发表的TPH基因多态性与自杀行为之间的关联研究。九项关于A218C TPH多态性与自杀行为之间的关联研究符合纳入标准。使用固定效应方法(优势比(OR)= 1.62;95%置信区间(CI)= [1.26;2.07])和随机效应方法(OR = 1.61;95% CI = [1.11;2.35])观察到A218C多态性与自杀行为之间存在显著关联。异质性来源分析表明,两项研究(一项阳性和一项阴性)显著偏离了计算出的总体效应。剔除这两项研究后进行的荟萃分析也显示TPH A218C多态性与自杀行为之间存在显著关联。两项分析均表明A等位基因对自杀行为风险具有剂量依赖性效应。