Guloksuz Sinan, Pries Lotta-Katrin, Delespaul Philippe, Kenis Gunter, Luykx Jurjen J, Lin Bochao D, Richards Alexander L, Akdede Berna, Binbay Tolga, Altınyazar Vesile, Yalınçetin Berna, Gümüş-Akay Güvem, Cihan Burçin, Soygür Haldun, Ulaş Halis, Cankurtaran EylemŞahin, Kaymak Semra Ulusoy, Mihaljevic Marina M, Petrovic Sanja Andric, Mirjanic Tijana, Bernardo Miguel, Cabrera Bibiana, Bobes Julio, Saiz Pilar A, García-Portilla María Paz, Sanjuan Julio, Aguilar Eduardo J, Santos José Luis, Jiménez-López Estela, Arrojo Manuel, Carracedo Angel, López Gonzalo, González-Peñas Javier, Parellada Mara, Maric Nadja P, Atbaşog Lu Cem, Ucok Alp, Alptekin Köksal, Saka Meram Can, Arango Celso, O'Donovan Michael, Rutten Bart P F, van Os Jim
Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University Medical Center, Maastricht, The Netherlands.
Department of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
World Psychiatry. 2019 Jun;18(2):173-182. doi: 10.1002/wps.20629.
Schizophrenia is a heritable complex phenotype associated with a background risk involving multiple common genetic variants of small effect and a multitude of environmental exposures. Early twin and family studies using proxy-genetic liability measures suggest gene-environment interaction in the etiology of schizophrenia spectrum disorders, but the molecular evidence is scarce. Here, by analyzing the main and joint associations of polygenic risk score for schizophrenia (PRS-SCZ) and environmental exposures in 1,699 patients with a diagnosis of schizophrenia spectrum disorders and 1,542 unrelated controls with no lifetime history of a diagnosis of those disorders, we provide further evidence for gene-environment interaction in schizophrenia. Evidence was found for additive interaction of molecular genetic risk state for schizophrenia (binary mode of PRS-SCZ above 75% of the control distribution) with the presence of lifetime regular cannabis use and exposure to early-life adversities (sexual abuse, emotional abuse, emotional neglect, and bullying), but not with the presence of hearing impairment, season of birth (winter birth), and exposure to physical abuse or physical neglect in childhood. The sensitivity analyses replacing the a priori PRS-SCZ at 75% with alternative cut-points (50% and 25%) confirmed the additive interaction. Our results suggest that the etiopathogenesis of schizophrenia involves genetic underpinnings that act by making individuals more sensitive to the effects of some environmental exposures.
精神分裂症是一种具有遗传性的复杂表型,与涉及多个小效应常见基因变异和多种环境暴露的背景风险相关。早期使用代理遗传易感性测量的双胞胎和家族研究表明,基因 - 环境相互作用在精神分裂症谱系障碍的病因学中起作用,但分子证据很少。在这里,通过分析1699例诊断为精神分裂症谱系障碍的患者和1542例无这些疾病终生诊断史的无关对照中精神分裂症多基因风险评分(PRS - SCZ)与环境暴露的主要和联合关联,我们为精神分裂症中的基因 - 环境相互作用提供了进一步的证据。发现精神分裂症分子遗传风险状态(PRS - SCZ高于对照分布的75%的二元模式)与终生定期使用大麻以及暴露于早期生活逆境(性虐待、情感虐待、情感忽视和欺凌)之间存在相加相互作用,但与听力障碍、出生季节(冬季出生)以及童年期遭受身体虐待或身体忽视无关。用替代切点(50%和25%)替换先验的75%的PRS - SCZ进行敏感性分析证实了相加相互作用。我们的结果表明,精神分裂症的病因涉及遗传基础,这些遗传基础通过使个体对某些环境暴露的影响更加敏感而起作用。