Mendelian Randomization Analysis Reveals Causal Effects of the Human Gut Microbiota on Abdominal Obesity

Author:

Xu Qian12,Zhang Shan-Shan1,Wang Rui-Rui1,Weng Yu-Jing1,Cui Xun1,Wei Xin-Tong12,Ni Jing-Jing13,Ren Hai-Gang14,Zhang Lei23,Pei Yu-Fang12

Affiliation:

1. Center of Translational Medicine, Taicang Affiliated Hospital of Soochow University, The First People's Hospital of Taicang, Department of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 215400, SuZhou, Jiangsu, PR China

2. Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, Medical College of Soochow University, 215123, SuZhou, Jiangsu, PR China

3. Center for Genetic Epidemiology and Genomics, School of Public Health, Medical College of Soochow University, 215123, SuZhou, Jiangsu, PR China

4. Laboratory of Molecular Neuropathology, Department of Pharmacology, School of Pharmaceutical Sciences, Medical College, Soochow University, 215123, SuZhou, PR China

Abstract

Abstract Background Although recent studies have revealed an association between the composition of the gut microbiota and obesity, whether specific gut microbiota cause obesity has not been determined. Objectives The aim of this study is to determine the causal relationship between specific gut microbiota and abdominal obesity. Based on genome-wide association study (GWAS) summary statistics, we performed a 2-sample Mendelian randomization (MR) analysis to evaluate whether the gut microbiota affects abdominal obesity. Methods Gut microbiota GWAS in 1126 twin pairs (age range, 18–89 years; 89% were females) from the TwinsUK study were used as exposure data. The primary outcome tested was trunk fat mass (TFM) GWAS in 492,805 participants (age range, 40–69 years; 54% were females) from the UK Biobank. The gut microbiota were classified at family, genus, and species levels. A feature was defined as a distinct family, genus, or species. MR analysis was mainly performed by an inverse variance–weighted test or Wald ratio test, depending on the number of instrumental variables (IVs) involved. A sensitivity analysis was performed on significant results by a weighted median test and a weighted genetic risk score (GRS) analysis. Results Results of MR analyses provided evidence of a causal association between 3 microbiota features and TFM, including 1 family [Lachnosiraceae; P = 0.02; β = 0.001 (SEE, 4.28 × 10−4)], 1 genus [Bifidobacterium; P = 5.0 × 10−9; β = −0.08 (SEE, 0.14)], and 1 species [Prausnitzii; P = 0.03; β = −0.007 (SEE, 0.003)]. Both the weighted median test and GRS analysis successfully validated the association of the genetically predicted family, Lachnosiraceae (Pweighted median = 0.03; PGRS = 0.004). Conclusions Our findings provided evidence of a causal association between gut microbiota and TFM in UK adults and identified specific bacteria taxa that may regulate the fat metabolism, thus offering new direction for the treatment of obesity.

Funder

National Natural Science Foundation of China

Undergraduate Training Program for Innovation and Entrepreneurship, Soochow University

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

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