Impact of gallstone disease on the risk of stroke and coronary artery disease: evidence from prospective observational studies and genetic analyses

孟德尔随机化 医学 冠状动脉疾病 冲程(发动机) 全基因组关联研究 置信区间 内科学 遗传关联 鹿特丹研究 疾病 心脏病学 生物信息学 遗传学 遗传变异 生物 基因 单核苷酸多态性 基因型 机械工程 工程类
作者
Li Zhang,Wenqiang Zhang,Lin He,Huijie Cui,Yutong Wang,Xueyao Wu,Xunying Zhao,Peijing Yan,Chao Yang,Changfeng Xiao,Mingshuang Tang,Lin Chen,Chenghan Xiao,Yanqiu Zou,Yunjie Liu,Yanfang Yang,Ling Zhang,Yuqin Yao,Jiayuan Li,Zhenmi Liu
出处
期刊:BMC Medicine [BioMed Central]
卷期号:21 (1) 被引量:3
标识
DOI:10.1186/s12916-023-03072-6
摘要

Abstract Background Despite epidemiological evidence associating gallstone disease (GSD) with cardiovascular disease (CVD), a dilemma remains on the role of cholecystectomy in modifying the risk of CVD. We aimed to characterize the phenotypic and genetic relationships between GSD and two CVD events – stroke and coronary artery disease (CAD). Methods We first performed a meta-analysis of cohort studies to quantify an overall phenotypic association between GSD and CVD. We then investigated the genetic relationship leveraging the largest genome-wide genetic summary statistics. We finally examined the phenotypic association using the comprehensive data from UK Biobank (UKB). Results An overall significant effect of GSD on CVD was found in meta-analysis (relative risk [RR] = 1.26, 95% confidence interval [CI] = 1.19–1.34). Genetically, a positive shared genetic basis was observed for GSD with stroke ( $${r}_{g}$$ r g =0.16, P = 6.00 × 10 –4 ) and CAD ( $${r}_{g}$$ r g =0.27, P = 2.27 × 10 –15 ), corroborated by local signals. The shared genetic architecture was largely explained by the multiple pleiotropic loci identified in cross-phenotype association study and the shared gene-tissue pairs detected by transcriptome-wide association study, but not a causal relationship (GSD to CVD) examined through Mendelian randomization (MR) (GSD-stroke: odds ratio [OR] = 1.00, 95%CI = 0.97–1.03; GSD-CAD: OR = 1.01, 95%CI = 0.98–1.04). After a careful adjustment of confounders or considering lag time using UKB data, no significant phenotypic effect of GSD on CVD was detected (GSD-stroke: hazard ratio [HR] = 0.95, 95%CI = 0.83–1.09; GSD-CAD: HR = 0.98, 95%CI = 0.91–1.06), further supporting MR findings. Conclusions Our work demonstrates a phenotypic and genetic relationship between GSD and CVD, highlighting a shared biological mechanism rather than a direct causal effect. These findings may provide insight into clinical and public health applications.
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