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2 型糖尿病与心房颤动:基于孟德尔随机化评估因果和多效通路。

Type 2 Diabetes and Atrial Fibrillation: Evaluating Causal and Pleiotropic Pathways Using Mendelian Randomization.

机构信息

National Heart and Lung Institute, Imperial College London London United Kingdom.

Papworth Hospital, Cambridge Biomedical Campus Cambridge United Kingdom.

出版信息

J Am Heart Assoc. 2023 Sep 5;12(17):e030298. doi: 10.1161/JAHA.123.030298. Epub 2023 Aug 23.

Abstract

Background Observational associations between type 2 diabetes (T2D) and atrial fibrillation (AF) have been established, but causality remains undetermined. We performed Mendelian randomization (MR) to study causal effects of genetically predicted T2D on AF risk, independent of cardiometabolic risk factors. Methods and Results Instrumental variables included 182 uncorrelated single nucleotide polymorphisms associated with T2D at genome-wide significance ( <5×10). Genetic association estimates for cardiometabolic exposures were obtained from genome-wide association studies including 188 577 individuals for low-density lipoprotein-C, 694 649 individuals for body mass index, and 757 601 for systolic blood pressure. Two-sample, inverse-variance weighted MR formed the primary analyses. The MR-TRYX approach was used to dissect potential pleiotropic pathways, with multivariable MR performed to investigate cardiometabolic mediation. Genetically predicted T2D associated with increased AF liability in univariable MR (odds ratio [OR], 1.08 [95% CI, 1.02-1.13], =0.003). Sensitivity analyses indicated potential pleiotropy, with radial MR identifying 4 outlier single nucleotide polymorphisms that were likely contributors. Phenomic scanning on MR-base and subsequent least absolute shrinkage and selection operator regression allowed prioritization of 7 candidate traits. The outlier-adjusted effect estimate remained consistent with the original inverse-variance weighted estimate (OR, 1.07 [95% CI, 1.02-1.12], =0.008). On multivariable MR, T2D remained associated with increased AF liability after adjustment for low-density lipoprotein-C and body mass index. Following adjustment for systolic blood pressure, the relationship between T2D and AF became nonsignificant (OR, 1.04 [95% CI, 0.95-1.13], =0.40). Conclusions These data provide novel genetic evidence that while T2D likely causally associates with AF, mediation via systolic blood pressure exists. Endeavoring to lower systolic blood pressure alongside achieving normoglycemia may provide particular benefit on AF risk in patients with T2D.

摘要

背景

已经确定 2 型糖尿病(T2D)和心房颤动(AF)之间存在观察性关联,但因果关系仍未确定。我们进行了孟德尔随机化(MR)研究,以研究遗传预测的 T2D 对 AF 风险的因果影响,而不受心脏代谢危险因素的影响。

方法和结果

工具变量包括与全基因组显著相关的 182 个与 T2D 无关的单核苷酸多态性(<5×10)。心脏代谢暴露的遗传关联估计值来自包括 188777 名个体的低密度脂蛋白-C、694649 名个体的体重指数和 757601 名个体的收缩压的全基因组关联研究。两样本,逆方差加权 MR 是主要分析方法。使用 MR-TRYX 方法来剖析潜在的多效性途径,使用多变量 MR 来研究心脏代谢中介作用。单变量 MR 显示,遗传预测的 T2D 与 AF 易感性增加相关(优势比[OR],1.08[95%CI,1.02-1.13],=0.003)。敏感性分析表明存在潜在的多效性,径向 MR 确定了 4 个可能是贡献者的异常单核苷酸多态性。在 MR-base 上进行表型扫描,并随后进行最小绝对收缩和选择算子回归,允许对 7 个候选特征进行优先级排序。异常调整后的效应估计与原始逆方差加权估计一致(OR,1.07[95%CI,1.02-1.12],=0.008)。在多变量 MR 中,在调整低密度脂蛋白-C 和体重指数后,T2D 与 AF 易感性增加仍相关。在调整收缩压后,T2D 与 AF 之间的关系变得不显著(OR,1.04[95%CI,0.95-1.13],=0.40)。

结论

这些数据提供了新的遗传证据,表明尽管 T2D 可能与 AF 有因果关系,但通过收缩压存在中介作用。在 T2D 患者中,努力降低收缩压并同时实现血糖正常化可能对 AF 风险有特殊益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629c/10547336/fa5d22623b01/JAH3-12-e030298-g001.jpg

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