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.
Front Immunol. 2024 Mar 15;15:1348347. doi: 10.3389/fimmu.2024.1348347. eCollection 2024.
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.
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。
Int J Chron Obstruct Pulmon Dis. 2024
Front Cell Infect Microbiol. 2024
Eur J Gastroenterol Hepatol. 2024-7-1
Diabetes Metab Syndr Obes. 2025-7-17
Front Immunol. 2025-5-30
BMC Microbiol. 2025-4-27
Front Cell Infect Microbiol. 2025-2-24
Philos Trans R Soc Lond B Biol Sci. 2023-10-23
Cell Death Discov. 2023-7-1
Front Cell Infect Microbiol. 2023