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Association of dementia with the 28-day mortality of sepsis: an observational and Mendelian randomization study

痴呆 败血症 医学 混淆 观察研究 孟德尔随机化 内科学 血管性痴呆 感染性休克 疾病 儿科 生物 生物化学 基因 基因型 遗传变异
作者
Ying Lan,Junchen Zhu,Peng Pu,Weiyi Ni,Qilin Yang,Lvlin Chen
出处
期刊:Frontiers in Aging Neuroscience [Frontiers Media]
卷期号:16
标识
DOI:10.3389/fnagi.2024.1417540
摘要

Background Observational research suggests that individuals with dementia who have sepsis face a higher likelihood of death. However, whether there is a causal relationship between the two remains unknown. Methods We analyzed data from patients diagnosed with sepsis and dementia, extracted from the Medical Information Mart for Intensive Care IV (MIMIC-IV) database. To examine the correlation between dementia and 28-day mortality in sepsis, we utilized Cox proportional hazards models. Following this, we performed a Mendelian randomization (MR) study with two samples to investigate the potential link between dementia and mortality within 28 days in sepsis. Results This study included a total of 22,189 patients diagnosed with sepsis, among whom 1,346 cases (6.1%) had dementia. After adjusting for multiple confounding factors, dementia was associated with an increased risk of 28-day mortality in sepsis (HR = 1.25, 95% CI = 1.12–1.39, p < 0.001). In the MR analysis, there appeared to be a causal relationship between genetically predicted dementia with Lewy bodies (DLB) (OR = 1.093, 95% CI = 1.016–1.177, p = 0.017) and 28-day mortality in sepsis. However, there was no evidence of causality between any dementia (OR = 1.063, 95% CI = 0.91–1.243, p = 0.437), Alzheimer’s disease (AD) (OR = 1.126, 95% CI = 0.976–1.299, p = 0.103), vascular dementia (VD) (OR = 1.008, 95% CI = 0.93–1.091, p = 0.844), and the risk of 28-day mortality in sepsis. Conclusion In the observational analysis, dementia was associated with an increased risk of 28-day mortality in septic patients. However, in the MR analysis, only DLB was associated with increased 28-day mortality in septic patients, with no observed correlation for other dementia subtypes.
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