循环脂肪因子水平与乳腺癌关系的孟德尔随机化研究OA
Mendelian randomization study on the relationship between circulating adipokines and breast cancer
目的 探讨循环脂肪因子与乳腺癌发生风险之间是否存在因果关系.方法 采用两样本孟德尔随机化研究设计将瘦素、脂联素、抵抗素(resistin,RETN)、脂肪酸结合蛋白4(fatty acid-binding protein 4,FABP4)表达水平相关的单核苷酸多态性作为工具变量,结局事件数据来自乳腺癌全基因组关联研究.采用逆方差加权法(inverse-variance weighted,IVW)、MR Egger、加权中位数法、简单模式法和加权模式法计算因果效应值.采用Cochran's Q检验检测异质性,MR Egger截距检验检测水平多效性,留一法进行敏感度分析.根据乳腺癌雌激素受体(estrogen receptor,ER)状态进行亚组分析.结果 IVW结果显示循环RETN和FABP4表达水平升高可增加ER+乳腺癌发生风险.留一法分析显示结果稳定.结论 循环RETN和FABP4水平可能与ER+乳腺癌发生存在因果关联.
Objective To investigate relationship between circulating adipokines and the risk of breast cancer.Methods Two-sample Mendelian randomization study design was employed,using single nucleotide polymorphisms associated with the expression levels of leptin,adiponectin,resistin(RETN),and fatty acid-binding protein 4(FABP4)as instrumental variables.Outcome event data were derived from the Breast Cancer Genome Wide Association Study.Causal effect values were calculated using inverse-variance weighted(IVW),MR Egger,weighted median,simple mode,and weighted mode methods.Heterogeneity was assessed using the Cochran's Q test,and horizontal heterogeneity was examined with the MR Egger intercept test.Sensitivity analysis was performed using the leave-one-out method.Subgroup analysis was conducted based on the estrogen receptor(ER)status in breast cancer.Results IVW analysis revealed that elevated circulating RETN and FABP4 expression levels were associated with increased risk of ER+breast cancer.The leave-one-out method analysis demonstrated stable results.Conclusion The circulating levels of RETN and FABP4 may be causally associated with the occurrence of ER+breast cancer.
陈思怡;夏嘉;徐群英;刘娅;叶运莉;李卉
西南医科大学公共卫生学院,四川 泸州 646000西南医科大学公共卫生学院,四川 泸州 646000西南医科大学公共卫生学院,四川 泸州 646000西南医科大学公共卫生学院,四川 泸州 646000西南医科大学公共卫生学院,四川 泸州 646000西南医科大学公共卫生学院,四川 泸州 646000
医药卫生
脂肪因子乳腺癌孟德尔随机化逆方差加权法
AdipokineBreast cancerMendelian randomizationInverse-variance weighted
《中国现代医生》 2026 (8)
19-25,7
四川省泸州市科技计划项目(2022-SYF-64)西南医科大学校级基金计划项目(2017-ZRQN-059)
评论