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.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
人人人完成签到,获得积分10
1秒前
2秒前
清爽半蕾完成签到,获得积分10
3秒前
4秒前
善良的越彬完成签到,获得积分10
4秒前
筱姐姐发布了新的文献求助10
6秒前
7秒前
7秒前
7秒前
iknj完成签到,获得积分10
8秒前
自由的飞扬完成签到,获得积分10
9秒前
10秒前
打打应助唠叨的轩轩采纳,获得10
10秒前
zzz发布了新的文献求助10
11秒前
完吐岁发布了新的文献求助10
11秒前
12秒前
奶酪完成签到 ,获得积分10
15秒前
17秒前
18秒前
Akim应助王赟赟采纳,获得10
18秒前
文献求助完成签到,获得积分10
18秒前
19秒前
小葵爸爸完成签到,获得积分10
21秒前
sdnumakabazi完成签到,获得积分10
21秒前
文献求助发布了新的文献求助10
22秒前
24秒前
25秒前
蔡能涛发布了新的文献求助10
26秒前
梁白开发布了新的文献求助10
26秒前
27秒前
科研通AI6.3应助Zzoe_S采纳,获得10
27秒前
上上签完成签到,获得积分20
28秒前
29秒前
SciGPT应助打倒恶人采纳,获得10
29秒前
Hungrylunch发布了新的文献求助10
30秒前
赘婿应助文献求助采纳,获得10
32秒前
34秒前
34秒前
穆世开发布了新的文献求助10
34秒前
有魅力的又菱完成签到,获得积分10
34秒前
高分求助中
Signals, Systems, and Signal Processing 610
Annie Ernaux: De la perte au corps glorieux 600
Petrology and Plate Tectonics,2025 500
Circular Polar Constellations Providing Continuous Single or Multiple Coverage Above a Specified Latitude 400
Burger's Medicinal Chemistry and Drug Discovery 400
Probability and Stochastic Processes 333
New directions for experimental lessons in science teaching: Myth, Mystery, Necessity? by Emily K. da Silva Cunha Souto (Author), Flávia Lins Silva (Author) 333
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6746590
求助须知:如何正确求助?哪些是违规求助? 8476563
关于积分的说明 18079484
捐赠科研通 6019248
什么是DOI,文献DOI怎么找? 3005147
邀请新用户注册赠送积分活动 1981923
关于科研通互助平台的介绍 1948628