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病毒感染与结直肠癌风险之间的遗传易感性关联:一项两样本孟德尔随机化分析。

Genetic susceptibility association between viral infection and colorectal cancer risk: a two-sample Mendelian randomization analysis.

作者信息

Li Gen, Wang Siyu, Ma Jianli, Liu Shanshan

机构信息

Department of Radiotherapy, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China.

出版信息

Infect Agent Cancer. 2024 Aug 10;19(1):37. doi: 10.1186/s13027-024-00602-6.

Abstract

BACKGROUND

The genetic susceptibility association between viral infection and the risk of colorectal cancer (CRC) has not been established.

METHODS

We conducted two-sample Mendelian randomization (MR) analysis using genome-wide association study (GWAS) data. In addition to traditional MR methods, we employed several other approaches, including cML, ConMix, MR-RAPS, and dIVW, to comprehensively assess causal effects. Sensitivity analyses were also performed to ensure the robustness of the results.

RESULTS

After sensitivity analysis, presence of SNPs linked to increased susceptibility to cold sores infection was found to decrease the risk of CRC (OR: 0.73, 95% CI: 0.57-0.93, P = 0.01). In subgroup analysis, presence of SNPs linked to increased susceptibility to viral hepatitis (OR: 0.89, 95% CI: 0.81-0.98, P = 0.02) and infectious mononucleosis (OR: 0.91, 95% CI: 0.84-0.98, P = 0.02) were associated with a decreased risk of colon cancer, while measles virus (OR: 1.41, 95% CI: 1.07-1.85, P = 0.01) was associated with an increased risk of colon cancer. Presence of SNPs linked to increased susceptibility to herpes zoster (OR: 1.26, 95% CI: 1.05-1.52, P = 0.01) was associated with an increased risk of rectal cancer, while infectious mononucleosis (OR: 0.809, 95% CI: 0.80-0.98, P = 0.02) was associated with a decreased risk.

CONCLUSION

The study provides the first evidence of the genetic susceptibility associations between different viral infections and CRC, enhancing our understanding of the etiology of CRC.

摘要

背景

病毒感染与结直肠癌(CRC)风险之间的遗传易感性关联尚未确定。

方法

我们使用全基因组关联研究(GWAS)数据进行了两样本孟德尔随机化(MR)分析。除了传统的MR方法外,我们还采用了其他几种方法,包括cML、ConMix、MR-RAPS和dIVW,以全面评估因果效应。还进行了敏感性分析以确保结果的稳健性。

结果

经过敏感性分析,发现与唇疱疹感染易感性增加相关的单核苷酸多态性(SNP)的存在会降低CRC风险(比值比:0.73,95%置信区间:0.57-0.93,P = 0.01)。在亚组分析中,与病毒性肝炎易感性增加相关的SNP的存在(比值比:0.89,95%置信区间:0.81-0.98,P = 0.02)和传染性单核细胞增多症(比值比:0.91,95%置信区间:0.84-0.98,P = 0.02)与结肠癌风险降低相关,而麻疹病毒(比值比:1.41,95%置信区间:1.07-1.85,P = 0.01)与结肠癌风险增加相关。与带状疱疹易感性增加相关的SNP的存在(比值比:1.26,95%置信区间:1.05-1.52,P = 0.01)与直肠癌风险增加相关,而传染性单核细胞增多症(比值比:0.809,95%置信区间:0.80-0.98,P = 0.02)与风险降低相关。

结论

该研究提供了不同病毒感染与CRC之间遗传易感性关联的首个证据,增进了我们对CRC病因的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/892e/11316422/e5cd6ecae735/13027_2024_602_Fig1_HTML.jpg

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