Romanovsky Eva, Choudhary Ashwani, Peles David, Abu-Akel Ahmad, Stern Shani
Sagol Department of Neurobiology, Faculty of Natural Sciences, University of Haifa, Haifa, Israel.
Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
Mol Psychiatry. 2025 Mar;30(3):1019-1028. doi: 10.1038/s41380-024-02740-0. Epub 2024 Sep 5.
Autism spectrum disorders (ASDs) are highly heritable and result in abnormal repetitive behaviors and impairment in communication and cognitive skills. Previous studies have focused on the genetic correlation between ASDs and other neuropsychiatric disorders, but an in-depth understanding of the correlation to other disorders is required. We conducted an extensive meta-analysis of common variants identified in ASDs by genome-wide association studies (GWAS) and compared it to the consensus genes and single nucleotide polymorphisms (SNPs) of Schizophrenia (SCZ). We found approximately 75% of the GWAS genes that are associated with ASD are also associated with SCZ. We further investigated the cellular phenotypes of neurons derived from induced pluripotent stem cell (iPSC) models in ASD and SCZ. Our findings revealed that ASD and SCZ neurons initially follow divergent developmental trajectories compared to control neurons. However, despite these early diametrical differences, both ASD and SCZ neurons ultimately display similar deficits in synaptic activity as they mature. This significant genetic overlap between ASD and SCZ, coupled with the convergence towards similar synaptic deficits, highlights the intricate interplay of genetic and developmental factors in shaping the shared underlying mechanisms of these complex neurodevelopmental and neuropsychiatric disorders.
自闭症谱系障碍(ASD)具有高度遗传性,会导致异常重复行为以及沟通和认知技能受损。以往的研究聚焦于ASD与其他神经精神疾病之间的遗传相关性,但仍需要深入了解其与其他疾病的相关性。我们对全基因组关联研究(GWAS)在ASD中鉴定出的常见变异进行了广泛的荟萃分析,并将其与精神分裂症(SCZ)的共识基因和单核苷酸多态性(SNP)进行了比较。我们发现,约75%与ASD相关的GWAS基因也与SCZ相关。我们进一步研究了源自诱导多能干细胞(iPSC)模型的ASD和SCZ神经元的细胞表型。我们的研究结果表明,与对照神经元相比,ASD和SCZ神经元最初遵循不同的发育轨迹。然而,尽管早期存在这些截然相反的差异,但ASD和SCZ神经元在成熟时最终都表现出相似的突触活动缺陷。ASD和SCZ之间这种显著的遗传重叠,再加上趋向于相似的突触缺陷,凸显了遗传和发育因素在塑造这些复杂神经发育和神经精神疾病共同潜在机制中的复杂相互作用。