Guillen-Burgos Hernan F, Vanegas Valentina, Gonzalez Isabella, Caicedo Ana M, Arango Valentina, Galvez-Florez Juan F, Anaya Juan-Manuel, McIntyre Roger S, Terán Wilson
Universidad Simón Bolivar, Center for Clinical and Translational Research, Barranquilla, Colombia.
Center for Clinical and Translational Research, Bogotá, Colombia.
Brain Behav. 2025 Sep;15(9):e70742. doi: 10.1002/brb3.70742.
The study explores shared genetic architecture among major psychiatric disorders-major depressive disorder, bipolar disorder, schizophrenia, and post-traumatic stress disorder-emphasizing their overlapping molecular pathways. Using public datasets, we identified shared genes and examined their functional implications through protein-protein interaction (PPI) networks and gene set enrichment analysis (GSEA).
Genes associated with each disorder were identified through the NCBI Gene database. Intersection analyses of gene sets were conducted using R to identify overlaps among the four disorders. STRING was used to predict PPI and conduct clustering analyses. Gene set enrichment analysis was performed to explore biological pathways, molecular functions, and cellular components.
We identified 31 intersected genes across all four disorders. PPI analyses demonstrated significant network enrichment, revealing interconnected pathways related to inflammation, neurotransmission, and synaptic plasticity. Functional enrichment highlighted pathways such as cytokines signaling, dopaminergic transmission, and synaptic vesicle cycling. Tissue expression analysis indicated significant involvement of brain regions, including the anterior cingulate cortex and mesolimbic system.
This study underscores the shared genetic underpinnings of severe psychiatric disorders, highlighting common biological processes, such as pro-inflammatory markers and synaptic signaling. These findings offer a transdiagnostic perspective, potentially informing novel therapeutic strategies for overlapping psychiatric conditions.
本研究探讨了主要精神疾病(重度抑郁症、双相情感障碍、精神分裂症和创伤后应激障碍)之间共享的遗传结构,重点关注它们重叠的分子途径。我们使用公共数据集,识别出共享基因,并通过蛋白质-蛋白质相互作用(PPI)网络和基因集富集分析(GSEA)研究了它们的功能意义。
通过NCBI基因数据库识别与每种疾病相关的基因。使用R进行基因集的交集分析,以确定四种疾病之间的重叠部分。利用STRING预测蛋白质-蛋白质相互作用并进行聚类分析。进行基因集富集分析以探索生物学途径、分子功能和细胞成分。
我们在所有四种疾病中识别出31个交集基因。蛋白质-蛋白质相互作用分析显示出显著的网络富集,揭示了与炎症、神经传递和突触可塑性相关的相互连接的途径。功能富集突出了细胞因子信号传导、多巴胺能传递和突触小泡循环等途径。组织表达分析表明大脑区域(包括前扣带回皮质和中脑边缘系统)有显著参与。
本研究强调了严重精神疾病共享的遗传基础,突出了诸如促炎标志物和突触信号传导等共同的生物学过程。这些发现提供了一种跨诊断的视角,可能为重叠精神疾病的新型治疗策略提供信息。