Department of Psychosis Studies, Institute of Psychiatry, King's College London , London , UK.
Department of Health Services and Population Research, Institute of Psychiatry, King's College London , London , UK.
Front Psychiatry. 2014 Jul 17;5:84. doi: 10.3389/fpsyt.2014.00084. eCollection 2014.
Failure to account for the etiological diversity that typically occurs in psychiatric cohorts may increase the potential for confounding as a proportion of genetic variance will be specific to exposures that have varying distributions in cases. This study investigated whether minimizing the potential for such confounding strengthened the evidence for a genetic candidate currently unsupported at the genome-wide level.
Two hundred and ninety-one first-episode psychosis cases from South London, UK and 218 unaffected controls were evaluated for a functional polymorphism at the rs1360780 locus in FKBP5. The relationship between FKBP5 and psychosis was modeled using logistic regression. Cannabis use (Cannabis Experiences Questionnaire) and parental separation (Childhood Experience of Care and Abuse Questionnaire) were included as confounders in the analysis.
Association at rs1360780 was not detected until the effects of the two environmental factors had been adjusted for in the model (OR = 2.81, 95% CI 1.23-6.43, p = 0.02). A statistical interaction between rs1360780 and parental separation was confirmed by stratified tests (OR = 2.8, p = 0.02 vs. OR = 0.89, p = 0.80). The genetic main effect was directionally consistent with findings in other (stress-related) clinical phenotypes. Moreover, the variation in effect magnitude was explained by the level of power associated with different cannabis constructs used in the model (r = 0.95).
Our results suggest that the extent to which genetic variants in FKBP5 can influence susceptibility to psychosis may depend on other etiological factors. This finding requires further validation in large independent cohorts. Potentially this work could have translational implications; the ability to discriminate between genetic etiologies based on a case-by-case understanding of previous environmental exposures would confer an important clinical advantage that would benefit the delivery of personalizable treatment strategies.
如果未能考虑到精神科队列中通常出现的病因多样性,那么作为遗传变异的一部分,混杂因素的潜在可能性将会增加,因为这些混杂因素与病例中分布不同的暴露因素有关。本研究旨在探讨是否可以通过最小化这种混杂的可能性来加强目前在全基因组水平上不支持的遗传候选物的证据。
本研究对来自英国伦敦南部的 291 例首发精神病病例和 218 例未受影响的对照者进行了 FKBP5 基因 rs1360780 功能多态性的评估。使用逻辑回归对 FKBP5 与精神病之间的关系进行建模。在分析中,将大麻使用(大麻经验问卷)和父母分离(儿童期经历关怀和虐待问卷)作为混杂因素。
直到模型中调整了两个环境因素的影响后,才检测到 rs1360780 的关联(OR=2.81,95%CI 1.23-6.43,p=0.02)。分层检验证实了 rs1360780 与父母分离之间的统计学相互作用(OR=2.8,p=0.02 与 OR=0.89,p=0.80)。遗传主要效应与其他(应激相关)临床表型的发现方向一致。此外,效应幅度的变化可以通过模型中使用的不同大麻结构的关联强度来解释(r=0.95)。
我们的结果表明,FKBP5 中的遗传变异对精神病易感性的影响程度可能取决于其他病因因素。这一发现需要在大型独立队列中进一步验证。这项工作可能具有转化意义;基于对以前环境暴露的逐个病例的理解来区分遗传病因的能力将带来重要的临床优势,从而有利于实施个性化治疗策略。