Department of Neurology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Clinical Systems Biology Laboratories, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Eur J Neurol. 2022 Jul;29(7):1913-1921. doi: 10.1111/ene.15332. Epub 2022 Apr 5.
Previous studies have reported the association between frailty and stroke or Alzheimer's disease (AD). However, the causality remains unclear. The aim of the present study was to evaluate whether genetically predicted frailty is associated with the risk of stroke or AD by a Mendelian randomization (MR) study.
Genetic variants associated with the frailty index (FI) were obtained from a large genome-wide association study (GWAS). Summary-level data for stroke and AD were adopted from the corresponding large GWAS of individuals of European ancestry. The inverse variance weighted method was used for estimating causal effects. Multivariable analysis was performed for further adjustment.
The present MR study indicated a suggestive association between genetically predicted FI and a higher risk of any stroke (odds ratio 1.360, 95% confidence interval 1.006-1.838, p = 0.046). Regarding the subtypes of stroke, genetically predicted FI was associated with a higher risk of large artery atherosclerosis stroke (LAS) (odds ratio 2.487, 95% confidence interval 1.282-4.826, p = 0.007). No causal links were identified between genetically predicted FI and any ischaemic stroke, intracranial haemorrhage, cardioembolic stroke, small artery stroke, AD or AD-by-proxy. Multivariable MR analysis indicated that the association of genetically predicted FI with LAS was attenuated after adjustment for inflammatory bowel disease (p = 0.114).
The MR study suggested that genetically predicted FI may be associated with an increased risk of any stroke. Subgroup analysis indicated a suggestive association between genetically predicted FI and the risk of LAS. The underlying mechanisms need further investigation.
先前的研究报告称,虚弱与中风或阿尔茨海默病(AD)之间存在关联。然而,因果关系尚不清楚。本研究旨在通过孟德尔随机化(MR)研究评估遗传预测的虚弱是否与中风或 AD 的风险相关。
从一项大型全基因组关联研究(GWAS)中获得与虚弱指数(FI)相关的遗传变异。采用欧洲血统个体相应的大型 GWAS 中的中风和 AD 的汇总水平数据。使用逆方差加权法估计因果效应。进行多变量分析以进一步调整。
本 MR 研究表明,遗传预测的 FI 与任何中风的风险增加之间存在关联(比值比 1.360,95%置信区间 1.006-1.838,p=0.046)。关于中风的亚型,遗传预测的 FI 与大动脉粥样硬化性中风(LAS)的风险增加相关(比值比 2.487,95%置信区间 1.282-4.826,p=0.007)。遗传预测的 FI 与任何缺血性中风、颅内出血、心源性栓塞性中风、小动脉中风、AD 或 AD 替代物之间未发现因果关系。多变量 MR 分析表明,在调整炎症性肠病后,遗传预测的 FI 与 LAS 的关联减弱(p=0.114)。
MR 研究表明,遗传预测的 FI 可能与中风风险增加相关。亚组分析表明,遗传预测的 FI 与 LAS 的风险之间存在关联。需要进一步研究潜在机制。