Department of Psychiatry and Psychotherapy, University Hospital, LMU Munich, Nußbaumstr. 7, 80336, Munich, Germany.
Laboratory of Neuroscience (LIM27), Institute of Psychiatry, University of São Paulo, São Paulo, Brazil.
J Neural Transm (Vienna). 2023 Mar;130(3):195-205. doi: 10.1007/s00702-022-02567-5. Epub 2022 Nov 12.
Since more than 3 decades, schizophrenia (SZ) has been regarded as a neurodevelopmental disorder. The neurodevelopmental hypothesis proposes that SZ is associated with genetic and environmental risk factors, which influence connectivity in neuronal circuits during vulnerable developmental periods. We carried out a non-systematic review of genetic/environmental factors that increase SZ risk in light of its neurodevelopmental hypothesis. We also reviewed the potential impact of SZ-related environmental and genetic risk factors on grey and white matter pathology and brain function based on magnetic resonance imaging and post-mortem studies. Finally, we reviewed studies that have used patient-derived neuronal models to gain knowledge of the role of genetic and environmental factors in early developmental stages. Taken together, these studies indicate that a variety of environmental factors may interact with genetic risk factors during the pre- or postnatal period and/or during adolescence to induce symptoms of SZ in early adulthood. These risk factors induce disturbances of macro- and microconnectivity in brain regions involving the prefrontal, temporal and parietal cortices and the hippocampus. On the molecular and cellular level, a disturbed synaptic plasticity, loss of oligodendrocytes and impaired myelination have been shown in brain regions of SZ patients. These cellular/histological phenotypes are related to environmental risk factors such as obstetric complications, maternal infections and childhood trauma and genetic risk factors identified in recent genome-wide association studies. SZ-related genetic risk may contribute to active processes interfering with synaptic plasticity in the adult brain. Advances in stem cell technologies are providing promising mechanistic insights into how SZ risk factors impact the developing brain. Further research is needed to understand the timing of the different complex biological processes taking place as a result of the interplay between genetic and environmental factors.
三十多年来,精神分裂症(SZ)一直被认为是一种神经发育障碍。神经发育假说提出,SZ 与遗传和环境风险因素有关,这些因素会在易受影响的发育期间影响神经元回路的连通性。我们根据神经发育假说,对增加 SZ 风险的遗传/环境因素进行了非系统性综述。我们还回顾了 SZ 相关环境和遗传风险因素对磁共振成像和尸检研究中灰质和白质病理学和脑功能的潜在影响。最后,我们回顾了使用患者来源的神经元模型来了解遗传和环境因素在早期发育阶段作用的研究。综上所述,这些研究表明,各种环境因素可能在产前或产后期间以及青春期与遗传风险因素相互作用,导致成年早期出现 SZ 症状。这些风险因素导致涉及前额叶、颞叶和顶叶皮层以及海马体的脑区的宏观和微观连通性紊乱。在分子和细胞水平上,SZ 患者的脑区显示出突触可塑性紊乱、少突胶质细胞丢失和髓鞘形成受损。这些细胞/组织表型与围产期并发症、母体感染和儿童创伤等环境风险因素以及最近全基因组关联研究中确定的遗传风险因素有关。SZ 相关的遗传风险可能会导致干扰成年人大脑突触可塑性的活跃过程。干细胞技术的进步为了解 SZ 风险因素如何影响发育中的大脑提供了有希望的机制见解。需要进一步研究以了解遗传和环境因素相互作用导致的不同复杂生物学过程发生的时间。