肠道微生物群、循环炎症蛋白与败血症:一项双向孟德尔随机研究

Zuming Li, Liangcai Lin, Yunqi Kong, Jieni Feng, Xiaolei Ren, Yushi Wang, Xueru Chen, Siyi Wu, Rongyuan Yang, Jiqiang Li, Yuntao Liu, Yue Lu, Jiankun Chen
{"title":"肠道微生物群、循环炎症蛋白与败血症:一项双向孟德尔随机研究","authors":"Zuming Li, Liangcai Lin, Yunqi Kong, Jieni Feng, Xiaolei Ren, Yushi Wang, Xueru Chen, Siyi Wu, Rongyuan Yang, Jiqiang Li, Yuntao Liu, Yue Lu, Jiankun Chen","doi":"10.3389/fcimb.2024.1398756","DOIUrl":null,"url":null,"abstract":"Gut microbiota is closely related to the occurrence and development of sepsis. However, the causal effects between the gut microbiota and sepsis, and whether circulating inflammatory proteins act as mediators, remain unclear.Gut microbiota, circulating inflammatory proteins, and four sepsis-related outcomes were identified from large-scale genome wide association studies (GWAS) summary data. Inverse Variance Weighted (IVW) was the primary statistical method. Additionally, we investigated whether circulating inflammatory proteins play a mediating role in the pathway from gut microbiota to the four sepsis-related outcomes.There were 14 positive and 15 negative causal effects between genetic liability in the gut microbiota and four sepsis-related outcomes. Additionally, eight positive and four negative causal effects were observed between circulating inflammatory proteins and the four sepsis-related outcomes. Circulating inflammatory proteins do not act as mediators.Gut microbiota and circulating inflammatory proteins were causally associated with the four sepsis-related outcomes. However, circulating inflammatory proteins did not appear to mediate the pathway from gut microbiota to the four sepsis-related outcomes.","PeriodicalId":505894,"journal":{"name":"Frontiers in Cellular and Infection Microbiology","volume":"21 24","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Gut microbiota, circulating inflammatory proteins and sepsis: a bi-directional Mendelian randomization study\",\"authors\":\"Zuming Li, Liangcai Lin, Yunqi Kong, Jieni Feng, Xiaolei Ren, Yushi Wang, Xueru Chen, Siyi Wu, Rongyuan Yang, Jiqiang Li, Yuntao Liu, Yue Lu, Jiankun Chen\",\"doi\":\"10.3389/fcimb.2024.1398756\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Gut microbiota is closely related to the occurrence and development of sepsis. However, the causal effects between the gut microbiota and sepsis, and whether circulating inflammatory proteins act as mediators, remain unclear.Gut microbiota, circulating inflammatory proteins, and four sepsis-related outcomes were identified from large-scale genome wide association studies (GWAS) summary data. Inverse Variance Weighted (IVW) was the primary statistical method. Additionally, we investigated whether circulating inflammatory proteins play a mediating role in the pathway from gut microbiota to the four sepsis-related outcomes.There were 14 positive and 15 negative causal effects between genetic liability in the gut microbiota and four sepsis-related outcomes. Additionally, eight positive and four negative causal effects were observed between circulating inflammatory proteins and the four sepsis-related outcomes. Circulating inflammatory proteins do not act as mediators.Gut microbiota and circulating inflammatory proteins were causally associated with the four sepsis-related outcomes. However, circulating inflammatory proteins did not appear to mediate the pathway from gut microbiota to the four sepsis-related outcomes.\",\"PeriodicalId\":505894,\"journal\":{\"name\":\"Frontiers in Cellular and Infection Microbiology\",\"volume\":\"21 24\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Cellular and Infection Microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3389/fcimb.2024.1398756\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Cellular and Infection Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fcimb.2024.1398756","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

肠道微生物群与败血症的发生和发展密切相关。肠道微生物群、循环炎症蛋白和四种败血症相关结果是从大规模全基因组关联研究(GWAS)的汇总数据中识别出来的。我们从大规模基因组广泛关联研究(GWAS)的汇总数据中确定了肠道微生物群、循环炎症蛋白和四种脓毒症相关结果。此外,我们还研究了循环炎症蛋白是否在从肠道微生物群到四种败血症相关结果的途径中起中介作用。此外,在循环炎症蛋白与四种败血症相关结果之间也观察到了 8 种正向因果效应和 4 种负向因果效应。肠道微生物群和循环炎症蛋白与四种败血症相关结果之间存在因果关系。然而,循环炎症蛋白似乎并不介导从肠道微生物群到四种败血症相关结果的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbiota, circulating inflammatory proteins and sepsis: a bi-directional Mendelian randomization study
Gut microbiota is closely related to the occurrence and development of sepsis. However, the causal effects between the gut microbiota and sepsis, and whether circulating inflammatory proteins act as mediators, remain unclear.Gut microbiota, circulating inflammatory proteins, and four sepsis-related outcomes were identified from large-scale genome wide association studies (GWAS) summary data. Inverse Variance Weighted (IVW) was the primary statistical method. Additionally, we investigated whether circulating inflammatory proteins play a mediating role in the pathway from gut microbiota to the four sepsis-related outcomes.There were 14 positive and 15 negative causal effects between genetic liability in the gut microbiota and four sepsis-related outcomes. Additionally, eight positive and four negative causal effects were observed between circulating inflammatory proteins and the four sepsis-related outcomes. Circulating inflammatory proteins do not act as mediators.Gut microbiota and circulating inflammatory proteins were causally associated with the four sepsis-related outcomes. However, circulating inflammatory proteins did not appear to mediate the pathway from gut microbiota to the four sepsis-related outcomes.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信