Causal relationship between gut microbiome and sex hormone‐binding globulin: A bidirectional two‐sample Mendelian randomization study

孟德尔随机化 性激素结合球蛋白 生物 激素 遗传学 内科学 内分泌学 医学 基因 基因型 雄激素 遗传变异
作者
Ziqiao Yan,Zheng Zheng,Tiantian Xia,Zhexin Ni,Yongqi Dou,Xinmin Liu
出处
期刊:American Journal of Reproductive Immunology [Wiley]
卷期号:91 (2) 被引量:5
标识
DOI:10.1111/aji.13824
摘要

Abstract Problem Currently, there is a variety of evidence linking the gut microbiota to changes in sex hormones. In contrast, the causal relationship between SHBG, a carrier of sex hormones, and the gut microbiota is unclear. Method of Study Bidirectional two‐sample Mendelian randomization (MR) analysis was used to detect the causal effect between SHBG and the gut microbiome. Summary statistics of genome‐wide association studies (GWASs) for the gut microbiome and SHBG were obtained from public datasets. Inverse‐variance weighting (IVW), weighted median, weighted mode, MR‐Egger and simple mode methods were used to operate the MR analysis. F ‐statistics and sensitivity analyses performed to evaluate bias and reliability. Results When we set gut microbiome as exposure and SHBG as outcome, we identified nine causal relationships. In males, Coprobacter (PIVW = 2.01 × 10 −6 ), Ruminococcus 2 (PIVW = 3.40 × 10 −5 ), Barnesiella (PIVW = 2.79 × 10 −2 ), Actinobacteria (PIVW = 3.25 × 10 −2 ) and Eubacterium fissicatena groups (PIVW = 3.64 × 10 −2 ) were associated with lower SHBG levels; Alphaproteobacteria (PIVW = 1.61 × 10 −2 ) is associated with higher SHBG levels. In females, Lachnoclostridium (PIVW = 9.75 × 10 −3 ) and Defluviitaleaceae UCG011 (PIVW = 3.67 × 10 −2 ) were associated with higher SHBG levels; Victivallaceae (PIVW = 2.23 × 10 −2 ) was associated with lower SHBG levels. According to the results of reverse MR analysis, three significant causal effect of SHBG was found on gut microbiota. In males, Dorea (PIVW = 4.17 × 10 −2 ) and Clostridiales (PIVW = 4.36 × 10 −2 ) were associated with higher SHBG levels. In females, Lachnoclostridium (PIVW = 7.44 × 10 −4 ) was associated with higherr SHBG levels. No signifcant heterogeneity of instrumental variables or horizontal pleiotropy was found in bidirectional two‐sample MR analysis. Conclusions This study may provide new insights into the causal relationship between the gut microbiome and sex hormone‐binding protein levels, as well as new treatment and prevention strategies for diseases such as abnormal changes in sex hormones.
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