Ishii Takaya, Wang Tao, Shibata Kazuki, Nishitani Shota, Yamanashi Takehiko, Wahba Nadia E, Seki Tomoteru, Thompson Kaitlyn J, Yamanishi Kyosuke, Nishiguchi Tsuyoshi, Shimura Akiyoshi, Aoyama Bun, Gorantla Nipun, Phuong Nathan J, Nguyen Hieu D, Santiago Therese A, Nishizawa Yoshitaka, Nagao Takaaki, Howard Mathew A, Kawasaki Hiroto, Hino Kyosuke, Ikeda Atsushi, Snyder Michael P, Shinozaki Gen
Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, California, USA.
Regenerative & Cellular Medicine Kobe Center, Sumitomo Pharma Co., Ltd., Osaka, Osaka, Japan.
bioRxiv. 2025 Mar 14:2025.03.13.643155. doi: 10.1101/2025.03.13.643155.
Post-operative delirium (POD) is a common complication after surgery especially in elderly patients, characterized by acute disturbances in consciousness and cognition, which negatively impacts long-term outcomes. Effective treatments remain elusive due to the unclear pathophysiology of POD. To address the knowledge gap, we investigated DNA methylation profiles and gene expression changes in brain cells from POD and non-POD patients who underwent brain resection surgery for medication refractory epilepsy. DNA methylation analysis revealed alteration in epigenetic status of immune and inflammation-related genes. Single-nucleus RNA sequencing (snRNAseq) identified POD-specific glial cell alterations, particularly in microglia, where neuroinflammation was strongly enhanced, consistent with epigenetic findings. Astrocytes exhibited changes in synapse-related functions and migration. Furthermore, downstream analysis indicated similarities between POD-associated glial cell states and pathologies such as encephalitis and dementia. Overall, this study-the first multi-omics analysis of brain tissue from POD patients-provides direct evidence of glial cell contributions to POD pathogenesis, and highlights potential therapeutic targets.
术后谵妄(POD)是手术后常见的并发症,尤其是在老年患者中,其特征为意识和认知的急性紊乱,会对长期预后产生负面影响。由于POD的病理生理学尚不清楚,有效的治疗方法仍然难以捉摸。为了填补这一知识空白,我们研究了接受药物难治性癫痫脑切除手术的POD患者和非POD患者脑细胞中的DNA甲基化谱和基因表达变化。DNA甲基化分析揭示了免疫和炎症相关基因表观遗传状态的改变。单核RNA测序(snRNAseq)确定了POD特异性胶质细胞改变,特别是在小胶质细胞中,神经炎症强烈增强,这与表观遗传学发现一致。星形胶质细胞在突触相关功能和迁移方面表现出变化。此外,下游分析表明POD相关胶质细胞状态与脑炎和痴呆等病理之间存在相似性。总体而言,这项对POD患者脑组织的首次多组学分析为胶质细胞对POD发病机制的贡献提供了直接证据,并突出了潜在的治疗靶点。