Cai Yongsong, Wang Jiachen, Wang Xinyi, Yuan Qiling, Xu Yan, Xu Peng
Department of Joint Surgery, Xi'an Honghui Hospital, Xi'an Jiaotong University Health Science Center, Xi'an 710054, People's Republic of China.
Geriatric Cardiopulmonary Rehabilitation Department, Shaanxi Provincial Rehabilitation Hospital, Xi'an, 710065, People's Republic of China.
J Affect Disord. 2024 Mar 15;349:69-76. doi: 10.1016/j.jad.2024.01.064. Epub 2024 Jan 8.
Our previous study found dementia as a significant risk factor for delirium development in elderly patients with hip fracture. However, the causal relationship between dementia and delirium remains unclear.
To assess the causal relationship between delirium and dementia, we conducted a bidirectional Mendelian randomization (MR) analysis. Inversevariance weighted (IVW), weighted median, MR Egger, weighted mode, and simple mode were employed to conduct the MR analysis. Heterogeneity was assessed using the Cochran Q statistic in MR-Egger and IVW methods. Horizontal pleiotropy was examined via the MR pleiotropy residual sum and outliers (MR-PRESSO) and MR-Egger intercept tests.
The forward MR analysis revealed a significant association between unclassified dementia (1.604 (1.326-1.941), p = 1.12 × 10), Alzheimer's disease (1.259 (1.128-1.405), p = 4.10 × 10), and dementia with Lewy bodies (1.121 (1.026-1.225), p = 0.011) with an increased risk of delirium. In the reverse MR analysis, delirium was also suggested to increase the risk of unclassified dementia (1.133 (1.066-1.204), p = 6.31 × 10) and vascular dementia (1.246 (1.075-1.444), p = 0.003). These significant results were further validated in the multivariable MR analysis. No evidence of heterogeneity or horizontal pleiotropy was observed (p > 0.05).
(1) Limited to European populations. (2) Sample population overlap between delirium and dementia. (3) Not all dementia subtypes were causally associated with delirium.
This study provides genetic evidence supporting a causal relationship between dementia and delirium, indicating that dementia may influence the risk of delirium while delirium may also increase the risk of dementia.
我们之前的研究发现痴呆是老年髋部骨折患者发生谵妄的一个重要危险因素。然而,痴呆与谵妄之间的因果关系仍不明确。
为了评估谵妄与痴呆之间的因果关系,我们进行了双向孟德尔随机化(MR)分析。采用逆方差加权(IVW)、加权中位数、MR-Egger、加权模式和简单模式进行MR分析。使用MR-Egger和IVW方法中的Cochran Q统计量评估异质性。通过MR多效性残差和离群值(MR-PRESSO)以及MR-Egger截距检验来检查水平多效性。
正向MR分析显示,未分类痴呆(1.604(1.326 - 1.941),p = 1.12×10)、阿尔茨海默病(1.259(1.128 - 1.405),p = 4.10×10)和路易体痴呆(1.121(1.026 - 1.225),p = 0.011)与谵妄风险增加之间存在显著关联。在反向MR分析中,谵妄也被认为会增加未分类痴呆(1.133(1.066 - 1.204),p = 6.31×10)和血管性痴呆(1.246(1.075 - 1.444),p = 0.003)的风险。这些显著结果在多变量MR分析中得到了进一步验证。未观察到异质性或水平多效性的证据(p > 0.05)。
(1)限于欧洲人群。(2)谵妄和痴呆的样本人群存在重叠。(3)并非所有痴呆亚型都与谵妄存在因果关联。
本研究提供了支持痴呆与谵妄之间因果关系的遗传学证据,表明痴呆可能影响谵妄风险,而谵妄也可能增加痴呆风险。