Liu Tongshuai, Bi Xia, Ma Fuguo, Chen Yanlin
Department of Anesthesiology, Qingdao Municipal Hospital, Qingdao, Shandong, China.
Department of Anesthesiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Brain Behav. 2025 Sep;15(9):e70811. doi: 10.1002/brb3.70811.
Observational research indicates that immune cells, in conjunction with circulating inflammatory proteins, could serve two functions in the development of delirium, despite the fact that the exact mechanisms remain ambiguous. The objective of this research is to identify the specific pathways through which immune cells trigger delirium and to evaluate the possible function of circulating inflammatory proteins as intermediaries.
A two-sample Mendelian randomization (MR) analysis was conducted using summary-level data from genome-wide association studies, which included 731 immune cells, 91 inflammatory proteins, and their association with delirium. The causal relationships between immune cells, inflammatory proteins, and delirium were systematically assessed through multivariable Mendelian randomization (multivariable MR). Following this, sensitivity analyses were performed using the Cochran Q test to evaluate heterogeneity, alongside MR-Egger tests to examine pleiotropy. Finally, a two-step methodology was employed to identify the inflammatory proteins that mediate the impact of immune cells on the onset of delirium.
Multivariable MR revealed 14 immune cell types that exhibited a causal relationship with delirium, along with 4 inflammatory proteins associated with this condition. Through a two-step analysis, it was determined that 2 inflammatory proteins mediate the influence of 2 immune cell phenotypes on delirium. Specifically, CD25 on IgD CDdim is linked to the inflammatory protein LIGHT, which accounts for a mediation percentage of 9.65%. Meanwhile, CD127 on CD45RA CD4, not Treg, is associated with the inflammatory protein CCL20, showing a mediation percentage of 9.78%.
This study conducted a thorough investigation into the causal relationships between immune cells and delirium, while also assessing the role of inflammatory proteins as mediators. The results aid in recognizing individuals who are at an elevated risk for experiencing delirium while also offering novel perspectives for proactive preventive measures and therapeutic strategies within clinical environments.
观察性研究表明,免疫细胞与循环炎症蛋白共同作用,在谵妄的发生发展中可能发挥两种功能,尽管确切机制仍不明确。本研究的目的是确定免疫细胞引发谵妄的具体途径,并评估循环炎症蛋白作为中介物的可能作用。
使用来自全基因组关联研究的汇总数据进行两样本孟德尔随机化(MR)分析,该研究包括731种免疫细胞、91种炎症蛋白及其与谵妄的关联。通过多变量孟德尔随机化(多变量MR)系统评估免疫细胞、炎症蛋白和谵妄之间的因果关系。在此之后,使用Cochran Q检验进行敏感性分析以评估异质性,同时使用MR-Egger检验检查多效性。最后,采用两步法确定介导免疫细胞对谵妄发作影响的炎症蛋白。
多变量MR显示有14种免疫细胞类型与谵妄存在因果关系,还有4种炎症蛋白与该病症相关。通过两步分析确定,2种炎症蛋白介导了2种免疫细胞表型对谵妄的影响。具体而言,IgD CDdim上的CD25与炎症蛋白LIGHT相关,其介导百分比为9.65%。同时,CD45RA CD4而非调节性T细胞上的CD127与炎症蛋白CCL20相关,显示介导百分比为9.78%。
本研究对免疫细胞与谵妄之间的因果关系进行了深入调查,同时评估了炎症蛋白作为介质的作用。研究结果有助于识别谵妄风险较高的个体,同时也为临床环境中的主动预防措施和治疗策略提供了新的视角。