Chair of Neuropsychopharmacology, Institute of Chemistry, University of Tartu, Ravila 14A Chemicum, 50411 Tartu, Estonia.
Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.
Neurosci Biobehav Rev. 2022 Aug;139:104757. doi: 10.1016/j.neubiorev.2022.104757. Epub 2022 Jun 29.
ADHD is a major burden in adulthood, where co-morbid conditions such as depression, substance use disorder and obesity often dominate the clinical picture. ADHD has substantial shared heritability with other mental disorders, contributing to comorbidity. However, environmental risk factors exist but their interaction with genetic makeup, especially in relation to comorbid disorders, remains elusive. This review for the first time summarizes present knowledge on gene x environment (GxE) interactions regarding the dopamine system. Hitherto, mainly candidate (GxE) studies were performed, focusing on the genes DRD4, DAT1 and MAOA. Some evidence suggest that the variable number tandem repeats in DRD4 and MAOA may mediate GxE interactions in ADHD generally, and comorbid conditions specifically. Nevertheless, even for these genes, common variants are bound to suggest risk only in the context of gender and specific environments. For other polymorphisms, evidence is contradictory and less convincing. Particularly lacking are longitudinal studies testing the interaction of well-defined environmental factors with polygenic risk scores reflecting the dopamine system in its entirety.
注意缺陷多动障碍(ADHD)在成年期是一个主要负担,其中共病情况,如抑郁症、物质使用障碍和肥胖症,往往主导着临床情况。ADHD 与其他精神障碍有很大的共同遗传基础,导致共病。然而,环境风险因素是存在的,但它们与遗传因素的相互作用,特别是与共病障碍的相互作用,仍然难以捉摸。这篇综述首次总结了目前关于多巴胺系统的基因与环境(GxE)相互作用的知识。迄今为止,主要进行了候选(GxE)研究,重点关注 DRD4、DAT1 和 MAOA 基因。有一些证据表明,DRD4 和 MAOA 中的可变数量串联重复可能介导 ADHD 以及共病的 GxE 相互作用。然而,即使对于这些基因,常见的变体也只能在性别和特定环境的背景下提示风险。对于其他多态性,证据是矛盾的,不太有说服力。特别缺乏的是测试明确界定的环境因素与反映整个多巴胺系统的多基因风险评分相互作用的纵向研究。