Lieber Institute for Brain Development.
Department of Psychiatry.
Schizophr Bull. 2017 Oct 21;43(6):1164-1168. doi: 10.1093/schbul/sbx118.
Since a proposal in 1986 that schizophrenia involved early neurodevelopmental deviations beginning in intrauterine life that showed varying expressivity as relevant neural systems matured, our understanding of the developmental components of the pathogenesis of schizophrenia has substantially evolved. This commentary highlights recent genetic and epigenetic evidence that prenatal development is a critical period for the expression of schizophrenia risk. Studies of gene expression have been fairly consistent in showing that genes implicated in schizophrenia show relatively greater expression during fetal than postnatal life. Consistent molecular evidence of early environmental perturbations contributing to risk has emerged from studies of epigenetic marks in the brain genome as potential environmental footprints and these also highlight the prenatal period. Analyses of gene expression in placenta dramatically identify the intrauterine environment as a direct point of impact of a component of schizophrenia genetic risk. Together, the enrichment of transcriptional and epigenetic associations with schizophrenia during fetal life suggest that both genetic and environmental risk for schizophrenia have a particular molecular impact on early development, possibly because of genetic biases in environmental sensitivity.
自 1986 年提出精神分裂症涉及宫内生命开始的早期神经发育偏差的观点以来,我们对精神分裂症发病机制的发育成分的理解有了很大的发展,相关的神经系统在成熟过程中表现出不同的表达能力。本评论强调了最近的遗传和表观遗传证据,表明产前发育是表达精神分裂症风险的关键时期。研究基因表达的结果相当一致,表明与精神分裂症相关的基因在胎儿期的表达相对大于出生后。来自对大脑基因组中表观遗传标记的研究,为风险的早期环境干扰提供了一致的分子证据,这些证据也突出了产前时期。对胎盘基因表达的分析明确将宫内环境确定为精神分裂症遗传风险因素的直接作用点。总的来说,胎儿期精神分裂症的转录和表观遗传关联的富集表明,精神分裂症的遗传和环境风险都对早期发育有特定的分子影响,这可能是由于对环境敏感性的遗传偏见。