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

IF 4.5 2区 医学 Q2 GERIATRICS & GERONTOLOGY Frontiers in Aging Neuroscience Pub Date : 2024-11-13 eCollection Date: 2024-01-01 DOI:10.3389/fnagi.2024.1417540
Ying Lan, Junchen Zhu, Peng Pu, Wentao Ni, Qilin Yang, Lvlin Chen
{"title":"Association of dementia with the 28-day mortality of sepsis: an observational and Mendelian randomization study.","authors":"Ying Lan, Junchen Zhu, Peng Pu, Wentao Ni, Qilin Yang, Lvlin Chen","doi":"10.3389/fnagi.2024.1417540","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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, <i>p</i> < 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, <i>p</i> = 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, <i>p</i> = 0.437), Alzheimer's disease (AD) (OR = 1.126, 95% CI = 0.976-1.299, <i>p</i> = 0.103), vascular dementia (VD) (OR = 1.008, 95% CI = 0.93-1.091, <i>p</i> = 0.844), and the risk of 28-day mortality in sepsis.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":12450,"journal":{"name":"Frontiers in Aging Neuroscience","volume":"16 ","pages":"1417540"},"PeriodicalIF":4.5000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11599188/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Aging Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fnagi.2024.1417540","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

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.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
痴呆症与败血症 28 天死亡率的关系:一项观察性和孟德尔随机研究。
背景:观察性研究表明,患有败血症的痴呆症患者死亡的可能性更高。然而,两者之间是否存在因果关系仍是未知数:我们分析了从重症监护医学信息市场 IV(MIMIC-IV)数据库中提取的被诊断患有败血症和痴呆症的患者数据。为了研究脓毒症患者痴呆症与 28 天死亡率之间的相关性,我们使用了 Cox 比例危险模型。随后,我们进行了一项孟德尔随机化(MR)研究,用两个样本来调查脓毒症患者痴呆症与 28 天内死亡率之间的潜在联系:本研究共纳入 22,189 名确诊为败血症的患者,其中 1,346 例(6.1%)患有痴呆症。在对多种混杂因素进行调整后,痴呆与脓毒症患者 28 天内死亡风险的增加有关(HR = 1.25,95% CI = 1.12-1.39,P < 0.001)。在 MR 分析中,遗传预测的路易体痴呆(DLB)(OR = 1.093,95% CI = 1.016-1.177,p = 0.017)与败血症 28 天死亡率之间似乎存在因果关系。然而,没有证据表明任何痴呆(OR = 1.063,95% CI = 0.91-1.243,p = 0.437)、阿尔茨海默病(AD)(OR = 1.126,95% CI = 0.976-1.299,p = 0.103)、血管性痴呆(VD)(OR = 1.008,95% CI = 0.93-1.091,p = 0.844)与败血症 28 天死亡风险之间存在因果关系:结论:在观察性分析中,痴呆与败血症患者 28 天死亡风险的增加有关。结论:在观察性分析中,痴呆与败血症患者 28 天死亡率增加的风险有关,但在 MR 分析中,只有 DLB 与败血症患者 28 天死亡率增加有关,而其他痴呆亚型则没有观察到相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience GERIATRICS & GERONTOLOGY-NEUROSCIENCES
CiteScore
6.30
自引率
8.30%
发文量
1426
期刊介绍: Frontiers in Aging Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the mechanisms of Central Nervous System aging and age-related neural diseases. Specialty Chief Editor Thomas Wisniewski at the New York University School of Medicine is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
期刊最新文献
Glial lactate metabolism and transport in Alzheimer's disease. Ultra-fast MRI for brain-age prediction in a real-world cognitive disorders clinic. PPARG as a central regulator of ferroptosis in Alzheimer's disease: integrated transcriptomic, single-cell, and experimental evidence. Correction: Glibenclamide attenuates neuroinflammation and promotes neurological recovery after intracerebral hemorrhage in aged rats. The role of healthy lifestyle in the association between hepatic fibro-inflammation and steatosis and brain aging-a cross-sectional study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1