Causal relationship between gut microbiota and gastric cancer: A two-sample Mendelian randomization analysis

被引:0
|
作者
Zhang, Jianling [1 ]
Dong, Chunlu [2 ]
Lin, Yanyan [2 ]
Shang, Lifeng [3 ]
Ma, Junming [4 ]
Hu, Ruiping [5 ]
Wang, Hejing [6 ]
机构
[1] First Hosp Lanzhou Univ, Gen Surg Ward 5, Lanzhou 730000, Gansu, Peoples R China
[2] First Hosp Lanzhou Univ, Gen Surg Ward 3, Lanzhou 730000, Gansu, Peoples R China
[3] Qingdao Eighth Peoples Hosp, Dept Gen Surg, Qingdao 266000, Shandong, Peoples R China
[4] Peoples Hosp Ningxia Hui Autonomous Reg, Dept Gen Surg, Yinchuan 750000, Ningxia, Peoples R China
[5] Third Peoples Hosp Gansu Prov, Dept Endocrinol, Lanzhou 730000, Gansu, Peoples R China
[6] Third Peoples Hosp Gansu Prov, Dept Healthcare Associated Infect Control, 763 Duanjiatan Rd, Lanzhou 730000, Gansu, Peoples R China
关键词
causal relationship; gut microbiota; gastric cancer; Mendelian randomization; genome-wide association study; INTESTINAL MICROBIOTA; METABOLITES; ACIDS;
D O I
10.3892/mco.2024.2736
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The gut microbiota is associated with GC; however, the causal association between the gut microbiota and GC remains to be determined. The aim of the present study was to investigate the causal association between gut microbiota and gastric cancer (GC) from the perspective of Mendelian randomization (MR). The present study performed MR analysis using summary statistics from a genome-wide association study of the gut microbiome and GC. Inverse-variance weighted, MR-Egger and weighted median methods were used to investigate the causal relationship between gut microbiota and GC. Heterogeneity tests were performed using Cochrane's Q statistic. Horizontal polytropy was detected using Mendelian Randomization Pleiotropy RESidual Sum and Outlier were eliminated. Estimates from MR indicated that nine gut microorganism remained stable with regard to acceptance of heterogeneity and sensitivity methods. Among them, the genera Prevotella 7, Roseburia and Ruminococcaceae UCG014 were associated with an increased risk of GC; by contrast, the family Enterobacteriaceae, the genera Allisonella, Lachnospiraceae FCS020, Ruminococcaceae UCG004 and Ruminococcaceae UCG009, and the order Enterobacteriales decreased the risk of GC development. The present study demonstrated the potential importance of modulating the abundance of gut microbiota for the prevention and treatment of GC.
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页数:7
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