Liu Huaigui, Xie Yingying, Ji Yuan, Zhou Yujing, Xu Jiayuan, Tang Jie, Liu Nana, Ding Hao, Qin Wen, Liu Feng, Yu Chunshui
Department of Radiology, Tianjin Key Lab of Functional Imaging & Tianjin Institute of Radiology, Tianjin Medical University General Hospital, Tianjin, China.
Department of Radiology, the First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Transl Psychiatry. 2025 Apr 16;15(1):150. doi: 10.1038/s41398-025-03348-w.
Both schizophrenia (SCZ) and Alzheimer's disease (AD) are highly heritable brain disorders. Despite of the observed comorbidity and shared psychosis and cognitive decline between the two disorders, the genetic risk architecture shared by SCZ and AD remains largely unknown. Based on summary statistics of the currently available largest genome-wide association studies for SCZ (n = 130,644) and AD (n = 455,258) in individuals of European ancestry, we conducted conditional/conjunctional false discovery rate (FDR) analysis to enhance the statistical power for discovering more genetic associations with SCZ or AD and to detect the common genetic variants shared by both disorders. We found shared genetic architecture in SCZ conditioned on AD and vice versa across different levels of significance, indicating polygenic overlap. We found 268 (78 novel) SCZ-only and 125 (55 novel) AD-only SNPs at conditional FDR < 0.01, and 16 lead SNPs shared by SCZ and AD at conjunctional FDR < 0.05. Only half of the shared SNPs showed concordant effect direction, which was consistent with the modest genetic correlation (r = 0.097; P = 0.026) between the two disorders. This study provides evidence for polygenic overlap between SCZ and AD, suggesting the existence of the shared molecular genetic mechanisms, which may inform therapeutic targets that are applicable for both disorders.
精神分裂症(SCZ)和阿尔茨海默病(AD)都是具有高度遗传性的脑部疾病。尽管观察到这两种疾病存在共病现象,且有共同的精神病性症状和认知衰退,但SCZ和AD共有的遗传风险结构在很大程度上仍不为人知。基于目前针对欧洲血统个体的SCZ(n = 130,644)和AD(n = 455,258)开展的最大规模全基因组关联研究的汇总统计数据,我们进行了条件/联合错误发现率(FDR)分析,以提高发现更多与SCZ或AD相关的遗传关联的统计效力,并检测这两种疾病共有的常见遗传变异。我们发现在不同显著性水平下,以AD为条件时SCZ存在共享遗传结构,反之亦然,这表明存在多基因重叠。在条件FDR < 0.01时,我们发现了268个(78个为新发现)仅与SCZ相关的单核苷酸多态性(SNP)和125个(55个为新发现)仅与AD相关的SNP,在联合FDR < 0.05时,发现了16个SCZ和AD共有的领先SNP。只有一半的共享SNP显示出一致的效应方向,这与两种疾病之间适度的遗传相关性(r = 0.097;P = 0.026)相符。本研究为SCZ和AD之间的多基因重叠提供了证据,表明存在共享的分子遗传机制,这可能为适用于这两种疾病的治疗靶点提供线索。