An atlas on risk factors for gastrointestinal cancers: A systematic review of Mendelian randomization studies

被引:2
|
作者
Huang, Yi-Xuan [1 ,2 ]
Wu, Jun-Hua [2 ]
Zhao, Yu-Qiang [2 ]
Sui, Wan-Nian [3 ]
Tian, Tian [2 ]
Han, Wen-Xiu [2 ,3 ]
Ni, Jing [2 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Dept Endocrinol, Hefei, Peoples R China
[2] Anhui Med Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Hefei 230032, Peoples R China
[3] Anhui Med Univ, Affiliated Hosp 1, Dept Gastrointestinal Surg, Dept Gen Surg, Hefei, Peoples R China
基金
中国国家自然科学基金;
关键词
Gastrointestinal cancers; Mendelian randomization; GWAS; Comorbidities; Gut microbiota; HEPATOCELLULAR-CARCINOMA RISK; SITE-SPECIFIC CANCERS; BODY-MASS INDEX; COLORECTAL-CANCER; ESOPHAGEAL CANCER; TELOMERE LENGTH; PANCREATIC-CANCER; GUT MICROBIOTA; CAUSAL ASSOCIATIONS; GLYCEMIC TRAITS;
D O I
10.1016/j.ypmed.2024.108147
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: Gastrointestinal cancers are one of the most frequent cancer types and seriously threaten human life and health. Recent studies attribute the occurrence of gastrointestinal cancers to both genetic and environmental factors, yet the intrinsic etiology remains unclear. Mendelian randomization is a powerful well-established statistical method that is based on genome-wide association study (GWAS) to evaluate the causal relationship between exposures and outcomes. In the present study, we aimed to conduct a systematic review of Mendelian randomization studies investigating any causal risk factors for gastrointestinal cancers. Methods: We systematically searched Mendelian randomization studies that addressed the associations of genetically predicted exposures with five main gastrointestinal cancers from September 2014 to March 2024, as well as testing the research quality and validity. Results: Our findings suggested robust and consistent causal effects of body mass index (BMI), basal metabolic rate, fatty acids, total cholesterol, total bilirubin, insulin like growth factor-1, eosinophil counts, interleukin 2, alcohol consumption, coffee consumption, apolipoprotein B on colorectal cancer risks, BMI, waist circumference, low-density lipoprotein (LDL), total testosterone, smoking on gastric cancer risks, BMI, fasting insulin, LDL, waist circumference, visceral adipose tissue (VAT), immune cells, type 2 diabetes mellitus (T2DM) on pancreatic cancer risks, waist circumference, smoking, T2DM on esophageal adenocarcinoma risks, and VAT, ferritin, transferrin, alcohol consumption, hepatitis B virus infection, rheumatoid arthritis on liver cancer risks, respectively. Conclusion: Larger, well-designed Mendelian randomization studies are practical in determining the causal status of risk factors for diseases.
引用
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页数:11
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