Causal effects of specific gut microbiota on spinal stenosis diseases: a two-sample mendelian randomization study

被引:0
|
作者
Luo, Kaihang [1 ]
Zeng, Weizheng [1 ]
Li, Qiushuang [1 ]
Zhang, Yuliang [2 ]
Liu, Shengkai [1 ]
Liu, Xizhe [1 ]
Liu, Shaoyu [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Spine Surg, Guangzhou, Peoples R China
[2] Guangdong Prov Clin Res Ctr Obstet & Gynecol, Guangdong Prov Key Lab Major Obstet Dis, Guangdong Hong Kong Macao Greater Bay Area Higher, Dept Obstet & Gynecol, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
gut microbiota; adolescent idiopathic scoliosis; lumbar spondylolisthesis; spinal stenosis; mendelian randomization; ADOLESCENT IDIOPATHIC SCOLIOSIS; VITAMIN-D; EPIDEMIOLOGY; PATHOGENESIS;
D O I
10.3389/fgene.2024.1400847
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Although recent observational studies and clinical trials have indicated a strong association between the gut microbiota and spinal stenosis diseases, the causal relationship between them remains unclear.Methods Based on large-scale genome-wide association studies, we employed two-sample Mendelian randomization (MR) to analyse the causal relationships between the gut microbiota (GM) and 3 spinal stenosis diseases: adolescent idiopathic scoliosis (AIS), lumbar spondylolisthesis (LS), and spinal stenosis (SS). MR analysis was performed using the inverse variance weighting (IVW) method as the primary approach, supplemented by MR-Egger regression, weighted median, and weighted mode analyses. MR-PRESSO and MR-Egger regression were employed to assess horizontal pleiotropy. Cochran's Q test was used to evaluate heterogeneity. Further leave-one-out sensitivity analysis was conducted to ascertain the reliability of the causal relationships.Results The IVW method identified 9 gut microbiota taxa (9 genera) that were causally related to AIS, 14 taxa (4 phyla, 2 classes, 2 orders, 1 family, and 5 genera) to LS, and 4 taxa (2 classes, 1 order, and 1 genus) to SS. The Cochrane Q test results did not indicate heterogeneity. Moreover, both the MR-Egger intercept test and the MR-PRESSO global test demonstrated that our findings were robust against potential horizontal pleiotropy. Furthermore, leave-one-out analysis provided additional evidence supporting the reliability of our identified causal relationships.Conclusion Our findings have substantiated the potential causal impact of specific GM taxa on AIS, LS, and SS, thereby offering novel insights into the mechanisms mediated by the gut microbiota in these three diseases and laying the foundation for targeted preventive measures in further research.
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页数:19
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