首页|高密度脂蛋白胆固醇与结直肠癌关系的孟德尔随机化研究

高密度脂蛋白胆固醇与结直肠癌关系的孟德尔随机化研究

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目的 通过孟德尔随机化方法阐明高密度脂蛋白胆固醇(HDL-C)与结直肠癌(CRC)之间的因果关系.方法 使用全基因组关联研究数据集筛选遗传工具变量进行孟德尔随机化分析.主要包括五种方法:逆方差加权法、孟德尔随机化Egger法、加权中位数法、简单模式法以及加权模式法,其中逆方差加权法作为主要分析方法.敏感性分析验证结果的稳健性.结果 最终确定了41个与HDL-C相关的遗传工具变量.逆方差加权法(OR=0.84,95%CI:0.73~0.96,P=0.01)与加权中位数法(OR=0.82,95%CI:0.67~0.99,P=0.04)结果均表明遗传决定的HDL-C与CRC风险呈负相关.敏感性分析证明结果不存在异质性和水平多效性(P>0.05).结论 HDL-C与CRC风险存在因果关系,rs1077834可能是HDL-C影响CRC风险的关键所在.
Relationship Between High-Density Lipoprotein Cholesterol and Colorectal Cancer—A Mendelian Randomization Study
Objective To elucidate the causal relationship between high-density lipoprotein cholesterol(HDL-C)and colorectal cancer(CRC)through Mendelian randomization.Methods Mendelian randomi-zation analysis was conducted using genetic instrumental variables selected from a genome-wide association study dataset.The main methods included inverse variance weighted,MR-Egger,weighted median,simple mode,and weighted mode method;among which,inverse variance weighted method served as the primary analytical approach.Sensitivity analyses were performed to verify the robustness of results.Results A total of 41 genetic instrumental variables associated with HDL-C were identified.Inverse variance weighted method(OR=0.84,95% CI:0.73-0.96,P=0.01)and weighted median method(OR=0.82,95% CI:0.67-0.99,P=0.04)indicated a negative correlation between genetically-determined HDL-C and CRC risk.Sensitivity analyses confirmed the absence of heterogeneity and horizontal pleiotropy(P>0.05).Conclusion A causal relationship exists between HDL-C and CRC risk,with rs1077834 as a potential key determinant in the influence of HDL-C on CRC risk.

High-density lipoprotein cholesterolColorectal cancerMendelian randomization

袁晨东、舒旭峰、王小强、揭志刚

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330006 南昌,南昌大学第一附属医院普外科

330006 南昌,南昌大学第一附属医院医学创新中心

高密度脂蛋白胆固醇 结直肠癌 孟德尔随机化

国家自然科学基金

81960503

2024

肿瘤防治研究
湖北省卫生厅,中国抗癌协会,湖北省肿瘤医院

肿瘤防治研究

CSTPCD
影响因子:0.737
ISSN:1000-8578
年,卷(期):2024.51(10)