There Is No Direct Causal Relationship Between Coronary Artery Disease and Alzheimer Disease: A Bidirectional Mendelian Randomization Study

孟德尔随机化 医学 内科学 心脏病学 冠状动脉疾病 心肌梗塞 多效性 心力衰竭 优势比 疾病 生物化学 基因 表型 基因型 化学 遗传变异
作者
Aifang Zhong,Yejun Tan,Yaqiong Liu,Xiangping Chai,Weijun Peng
出处
期刊:Journal of the American Heart Association [Wiley]
卷期号:13 (15) 被引量:1
标识
DOI:10.1161/jaha.123.032814
摘要

Background The association between poor cardiovascular health and cognitive decline as well as dementia progression has been inconsistent across studies. This study used Mendelian randomization (MR) to investigate the causal relationship between Alzheimer disease (AD), circulating levels of total‐tau, and coronary artery disease (CAD). Methods and Results This study used MR to investigate the causal relationship between AD or circulating levels of total‐tau and CAD, including ischemic heart disease, myocardial infarction, coronary heart disease, coronary atherosclerosis, and heart failure. The primary analysis used the inverse‐variance weighted method, with pleiotropy and heterogeneity assessed using MR‐Egger regression and the Q statistic. The overall results of the MR analysis indicated that AD did not exhibit a causal effect on heart failure (odds ratio [OR], 0.969 [95% CI, 0.921–1.018]; P =0.209), myocardial infarction (OR, 0.972 [95% CI, 0.915–1.033]; P =0.359), ischemic heart disease (OR, 1.013 [95% CI, 0.949–1.082]; P =0.700), coronary heart disease (OR, 1.005 [95% CI, 0.937–1.078]; P =0.881), or coronary atherosclerosis (OR, 0.987 [95% CI, 0.926–1.052]; P =0.690). No significant causal effect of CAD was observed on AD in the reverse MR analysis. Additionally, our findings revealed that CAD did not influence circulating levels of total‐tau, nor did circulating levels of total‐tau increase the risk of CAD. Sensitivity analysis and assessment of horizontal pleiotropy suggested that these factors did not distort the causal estimates. Conclusions The findings of this study indicate the absence of a direct causal relationship between AD and CAD from a genetic perspective. Therefore, managing the 2 diseases should be more independent and targeted. Concurrently, investigating the mechanism underlying their comorbidity may not yield meaningful insights for advancing treatment strategies.

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
2秒前
Fiona娜娜发布了新的文献求助10
2秒前
斯文败类应助keyan采纳,获得10
2秒前
xavier完成签到 ,获得积分10
2秒前
奋斗瑶发布了新的文献求助10
2秒前
丘比特应助24采纳,获得10
3秒前
隐形曼青应助xdd采纳,获得10
4秒前
4秒前
4秒前
oaf完成签到 ,获得积分10
4秒前
4秒前
5秒前
5秒前
爱吃苹果完成签到,获得积分10
5秒前
kyt发布了新的文献求助10
6秒前
李爱国应助li采纳,获得10
6秒前
7秒前
7秒前
落伍少年完成签到,获得积分10
7秒前
科研通AI2S应助虚幻凡柔采纳,获得10
8秒前
LIN2QI完成签到,获得积分10
8秒前
9秒前
MarcusY发布了新的文献求助10
9秒前
代秋完成签到,获得积分10
9秒前
9秒前
山260完成签到 ,获得积分10
9秒前
从容道罡完成签到,获得积分10
9秒前
酷波er应助lyn采纳,获得10
10秒前
李爱国应助夏以宁采纳,获得10
11秒前
KevinLeng发布了新的文献求助10
11秒前
lhappy233完成签到,获得积分20
12秒前
12秒前
情怀应助尚尚尚采纳,获得50
12秒前
12秒前
er123721发布了新的文献求助10
13秒前
尹英宇发布了新的文献求助10
13秒前
cookie完成签到,获得积分10
14秒前
美丽的盼夏完成签到,获得积分20
14秒前
14秒前
烤匠喊你吃鱼完成签到 ,获得积分10
14秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
AnnualResearch andConsultation Report of Panorama survey and Investment strategy onChinaIndustry 1000
卤化钙钛矿人工突触的研究 1000
Engineering for calcareous sediments : proceedings of the International Conference on Calcareous Sediments, Perth 15-18 March 1988 / edited by R.J. Jewell, D.C. Andrews 1000
Continuing Syntax 1000
Signals, Systems, and Signal Processing 610
2026 Hospital Accreditation Standards 500
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 6264785
求助须知:如何正确求助?哪些是违规求助? 8086542
关于积分的说明 16900263
捐赠科研通 5335238
什么是DOI,文献DOI怎么找? 2839639
邀请新用户注册赠送积分活动 1817000
关于科研通互助平台的介绍 1670559