文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

肠道微生物组、血浆代谢组、外周细胞和炎症细胞因子对肥胖的影响:双向两样本孟德尔随机化研究和中介分析。

Effect of the gut microbiome, plasma metabolome, peripheral cells, and inflammatory cytokines on obesity: a bidirectional two-sample Mendelian randomization study and mediation analysis.

机构信息

Human Molecular Genetics Group, National Health Commission (NHC) Key Laboratory of Molecular Probes and Targeted Diagnosis and Therapy, The Fourth Affiliated Hospital, Harbin Medical University, Harbin, China.

Department of Child and Adolescent Health, School of Public Health, Harbin Medical University, Harbin, China.

出版信息

Front Immunol. 2024 Mar 15;15:1348347. doi: 10.3389/fimmu.2024.1348347. eCollection 2024.


DOI:10.3389/fimmu.2024.1348347
PMID:38558794
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10981273/
Abstract

BACKGROUND: Obesity is a metabolic and chronic inflammatory disease involving genetic and environmental factors. This study aimed to investigate the causal relationship among gut microbiota abundance, plasma metabolomics, peripheral cell (blood and immune cell) counts, inflammatory cytokines, and obesity. METHODS: Summary statistics of 191 gut microbiota traits (N = 18,340), 1,400 plasma metabolite traits (N = 8,299), 128 peripheral cell counts (blood cells, N = 408,112; immune cells, N = 3,757), 41 inflammatory cytokine traits (N = 8,293), and 6 obesity traits were obtained from publicly available genome-wide association studies. Two-sample Mendelian randomization (MR) analysis was applied to infer the causal links using inverse variance-weighted, maximum likelihood, MR-Egger, weighted median, weighted mode, and Wald ratio methods. Several sensitivity analyses were also utilized to ensure reliable MR results. Finally, we used mediation analysis to identify the pathway from gut microbiota to obesity mediated by plasma metabolites, peripheral cells, and inflammatory cytokines. RESULTS: MR revealed a causal effect of 44 gut microbiota taxa, 281 plasma metabolites, 27 peripheral cells, and 8 inflammatory cytokines on obesity. Among them, five shared causal gut microbiota taxa belonged to the phylum , order , family , genus UCG008, and species group. Furthermore, we screened 42 shared causal metabolites, 7 shared causal peripheral cells, and 1 shared causal inflammatory cytokine. Based on known causal metabolites, we observed that the metabolic pathways of D-arginine, D-ornithine, linoleic acid, and glycerophospholipid metabolism were closely related to obesity. Finally, mediation analysis revealed 20 mediation relationships, including the causal pathway from gut microbiota to obesity, mediated by 17 metabolites, 2 peripheral cells, and 1 inflammatory cytokine. Sensitivity analysis represented no heterogeneity or pleiotropy in this study. CONCLUSION: Our findings support a causal relationship among gut microbiota, plasma metabolites, peripheral cells, inflammatory cytokines, and obesity. These biomarkers provide new insights into the mechanisms underlying obesity and contribute to its prevention, diagnosis, and treatment.

摘要

背景:肥胖是一种涉及遗传和环境因素的代谢性和慢性炎症性疾病。本研究旨在探讨肠道微生物群落丰度、血浆代谢组学、外周细胞(血液和免疫细胞)计数、炎症细胞因子与肥胖之间的因果关系。

方法:从公开的全基因组关联研究中获取了 191 个肠道微生物特征(N=18340)、1400 个血浆代谢特征(N=8299)、128 个外周细胞计数(血细胞,N=408112;免疫细胞,N=3757)、41 个炎症细胞因子特征(N=8293)和 6 个肥胖特征的汇总统计数据。使用两样本 Mendelian 随机化(MR)分析,采用逆方差加权、最大似然、MR-Egger、加权中位数、加权模式和 Wald 比方法推断因果关系。还进行了几种敏感性分析,以确保可靠的 MR 结果。最后,我们使用中介分析来确定肠道微生物群通过血浆代谢物、外周细胞和炎症细胞因子对肥胖的中介途径。

结果:MR 揭示了 44 种肠道微生物群分类群、281 种血浆代谢物、27 种外周细胞和 8 种炎症细胞因子对肥胖的因果影响。其中,有 5 种共享的因果肠道微生物群分类群属于门、目、科、属 UCG008 和种组。此外,我们还筛选了 42 种共享的因果代谢物、7 种共享的因果外周细胞和 1 种共享的因果炎症细胞因子。基于已知的因果代谢物,我们观察到 D-精氨酸、D-鸟氨酸、亚油酸和甘油磷脂代谢途径与肥胖密切相关。最后,中介分析显示了 20 种中介关系,包括肠道微生物群到肥胖的因果途径,由 17 种代谢物、2 种外周细胞和 1 种炎症细胞因子介导。敏感性分析表明本研究无异质性或多效性。

结论:我们的研究结果支持肠道微生物群、血浆代谢物、外周细胞、炎症细胞因子与肥胖之间存在因果关系。这些生物标志物为肥胖的发病机制提供了新的见解,并有助于肥胖的预防、诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/8c6b36ce0949/fimmu-15-1348347-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/43b517f11e07/fimmu-15-1348347-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/2d5ec487eb2e/fimmu-15-1348347-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/65b4fb226e55/fimmu-15-1348347-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/8c6b36ce0949/fimmu-15-1348347-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/43b517f11e07/fimmu-15-1348347-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/2d5ec487eb2e/fimmu-15-1348347-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/65b4fb226e55/fimmu-15-1348347-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f07/10981273/8c6b36ce0949/fimmu-15-1348347-g004.jpg

相似文献

[1]
Effect of the gut microbiome, plasma metabolome, peripheral cells, and inflammatory cytokines on obesity: a bidirectional two-sample Mendelian randomization study and mediation analysis.

Front Immunol. 2024

[2]
Causal Effects of Gut Microbiota and Metabolites on Chronic Obstructive Pulmonary Disease: A Bidirectional Two Sample Mendelian Randomization Study.

Int J Chron Obstruct Pulmon Dis. 2024

[3]
Causal relationships between gut microbiota, plasma metabolites, and HIV infection: insights from Mendelian randomization and mediation analysis.

Virol J. 2024-8-30

[4]
Causal relationship between gut microbiota, plasma metabolites, inflammatory cytokines and abdominal aortic aneurysm: a Mendelian randomization study.

Clin Exp Hypertens. 2024-12-31

[5]
Genetic liability of gut microbiota for idiopathic pulmonary fibrosis and lung function: a two-sample Mendelian randomization study.

Front Cell Infect Microbiol. 2024

[6]
Potential mechanisms of gut microbiota influence on different types of vertigo: a bidirectional Mendelian randomization and mediation analysis.

BMC Neurol. 2024-8-27

[7]
The Effects of Specific Gut Microbiota and Metabolites on IgA Nephropathy-Based on Mendelian Randomization and Clinical Validation.

Nutrients. 2023-5-22

[8]
Exploring causal effects of gut microbiota and metabolites on body fat percentage using two-sample Mendelian randomization.

Diabetes Obes Metab. 2024-9

[9]
Causal effect between gut microbiota and gastroesophageal reflux disease: a bidirectional two-sample Mendelian randomization study.

Eur J Gastroenterol Hepatol. 2024-7-1

[10]
The causal relationship between gut microbiota and inflammatory dermatoses: a Mendelian randomization study.

Front Immunol. 2023

引用本文的文献

[1]
Associations between gut microbiome and circulating cytokines: a cross-sectional analysis in the FINRISK 2002 population cohort.

Gut Pathog. 2025-8-26

[2]
Dietary Influence on Urolithiasis Risk Mediated by Plasma Metabolites: A Mendelian Randomization and Experimental Study Linking Genes, Metabolites, and Clinical Outcomes.

Food Sci Nutr. 2025-8-19

[3]
Advances in Mendelian Randomization Studies of Obesity Over the Past Decade: Uncovering Key Genetic Mechanisms.

Diabetes Metab Syndr Obes. 2025-7-17

[4]
Cytokine concentration in peripheral blood of patients with childhood obesity.

Front Immunol. 2025-5-30

[5]
Sleep habits, brain functional networks, and type 2 diabetes risk: cohort studies from North American and Asian populations and mediating Mendelian randomization analyses.

Diabetol Metab Syndr. 2025-6-13

[6]
Gut Microbiota in Lactose Intolerance: A Mendelian Randomization Study on Microbial Mechanisms and Potential Links to Tumor Inflammatory Microenvironments.

Mediators Inflamm. 2025-6-5

[7]
Identification of 1,400 metabolites as mediators of obesity in 473 gut microbiota taxa: a mediation Mendelian randomization study.

Microbiol Spectr. 2025-6-3

[8]
Gut microbiome links obesity to type 2 diabetes: insights from Mendelian randomization.

BMC Microbiol. 2025-4-27

[9]
Causal Correlations Between Plasma Metabolites, Inflammatory Proteins, and Chronic Obstructive Pulmonary Disease: A Mendelian Randomization and Bioinformatics-Based Investigation.

J Inflamm Res. 2025-3-18

[10]
Differential effects of high-fat diet on salivary and gut microbiota.

Front Cell Infect Microbiol. 2025-2-24

本文引用的文献

[1]
The causal effects between gut microbiota and hemorrhagic stroke: a bidirectional two-sample Mendelian randomization study.

Front Microbiol. 2023-12-22

[2]
The gut microbiome in the fight against obesity: The potential of dietary factors.

FASEB J. 2023-11

[3]
Genetic evidence strengthens the bidirectional connection between gut microbiota and periodontitis: insights from a two-sample Mendelian randomization study.

J Transl Med. 2023-9-28

[4]
Obesity and Selected Allergic and Immunological Diseases-Etiopathogenesis, Course and Management.

Nutrients. 2023-8-31

[5]
Questioning the foundations of the gut microbiota and obesity.

Philos Trans R Soc Lond B Biol Sci. 2023-10-23

[6]
The role of CXCL family members in different diseases.

Cell Death Discov. 2023-7-1

[7]
Gut mycobiome in metabolic diseases: Mechanisms and clinical implication.

Biomed J. 2024-6

[8]
Causal effects of gut microbiota on the risk of periodontitis: a two-sample Mendelian randomization study.

Front Cell Infect Microbiol. 2023

[9]
The Human Gut Virome and Its Relationship with Nontransmissible Chronic Diseases.

Nutrients. 2023-2-15

[10]
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases.

Nat Genet. 2023-1

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索