Mendelian randomization analysis to investigate the gut microbiome in oral and oropharyngeal cancer

被引:4
|
作者
Zhang, Qihe [1 ,2 ]
Wang, Huanhuan [1 ,2 ,3 ,4 ]
Tian, Yuan [5 ]
Li, Jinjie [5 ]
Xin, Ying [5 ]
Jiang, Xin [1 ,2 ,3 ,4 ]
机构
[1] Jilin Univ, First Hosp Jilin Univ, Jilin Prov Key Lab Radiat Oncol & Therapy, Changchun, Peoples R China
[2] Jilin Univ, Minist Educ, Key Lab Pathobiol, Changchun, Peoples R China
[3] First Hosp Jilin Univ, Dept Radiat Oncol, Changchun, Peoples R China
[4] Jilin Univ, Sch Publ Hlth, NHC Key Lab Radiobiol, Changchun, Peoples R China
[5] Jilin Univ, Minist Educ, Key Lab Pathobiol, Changchun, Peoples R China
关键词
gut microbiome; oral cancer; oropharyngeal cancer; Mendelian randomization; meta-analysis; INTERNATIONAL HEAD; POOLED ANALYSIS; EPIDEMIOLOGY; INSTRUMENTS; RISK; BIAS;
D O I
10.3389/fcimb.2023.1210807
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundEvidence supports an observational association between the gut microbiome and susceptibility to extraintestinal cancers, but the causal relationship of this association remains unclear.MethodsTo identify the specific causal gut microbiota of oral and oropharyngeal cancer, we performed two-sample Mendelian randomization (MR) analysis of gut microbiota on oral and oropharyngeal cancer using a fixed-effects inverse-variance-weighted model. Gut microbiota across five different taxonomical levels from the MiBioGen genome-wide association study (GWAS) were used as exposures. Oral cancer, oropharyngeal cancer and a combination of the two cancers defined from three separate data sources were used as the outcomes. Odds ratios (ORs) and 95% confidence intervals (CIs) for disease per standard deviation (SD) higher abundance of microbiome.Results & ConclusionsThere was little evidence for a causal effect of gut microbiota on oral and oropharyngeal cancer when using a genome-wide p-value threshold for selecting instruments. Secondary analyses using a more lenient p-value threshold indicated that there were 90 causal relationships between 58 different microbial features but that sensitivity analyses suggested that these were possibly affected by violations of MR assumptions and were not consistent across MR methodologies or data sources and therefore are also to unlikely reflect causation. These findings provide new insights into gut microbiota-mediated oral and oropharyngeal cancers and warrant further investigation.
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页数:11
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