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没有前瞻性关联表明冠状动脉疾病的多基因风险评分与静脉血栓栓塞发生率之间存在关联。

No prospective association of a polygenic risk score for coronary artery disease with venous thromboembolism incidence.

机构信息

Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, USA.

Human Genetics Center, Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA.

出版信息

J Thromb Haemost. 2021 Nov;19(11):2841-2844. doi: 10.1111/jth.15501. Epub 2021 Aug 31.

Abstract

BACKGROUND

Previous studies are inconsistent about whether chronic coronary artery disease or generalized atherosclerosis is a causal risk factor for venous thromboembolism. No study seems to have taken a genomic approach to this question.

OBJECTIVE

To test in a prospective study whether a polygenic risk score for coronary artery disease is associated with risk of venous thromboembolism.

PARTICIPANTS/METHODS: Within the Atherosclerosis Risk in Communities Study cohort, we computed a previously validated polygenic risk score for coronary artery disease among 9144 White participants at baseline in 1987-1989. We followed the participants through 2015 for incident hospitalized venous thromboembolism events, validated by physician review. We used Cox proportional hazards regression to associate quintiles of the polygenic risk score to venous thromboembolism incidence rates.

RESULTS

Over the median of 26 years of follow-up, 476 participants had a venous thromboembolism event. There was no apparent association between the coronary artery disease polygenic risk score and incident venous thromboembolism, with age, sex, body mass index adjusted hazard ratios across quintiles being 1 (reference), 0.87 (0.65, 1.15), 1.08 (0.82, 1.42), 0.96 (0.72, 1.27), and 1.03 (0.78, 1.37).

CONCLUSIONS

A genetic disposition to coronary artery disease did not confer an increased risk of venous thromboembolism in this prospective study.

摘要

背景

先前的研究对于慢性冠状动脉疾病或全身性动脉粥样硬化是否是静脉血栓栓塞的因果风险因素存在不一致的结论。似乎没有研究从基因组学的角度来探讨这个问题。

目的

在一项前瞻性研究中,检测冠状动脉疾病的多基因风险评分与静脉血栓栓塞风险之间的相关性。

参与者/方法:在动脉粥样硬化风险社区研究队列中,我们在 1987-1989 年基线时对 9144 名白人参与者计算了之前验证过的冠状动脉疾病多基因风险评分。我们通过医生审查对参与者进行了静脉血栓栓塞事件的随访,直到 2015 年。我们使用 Cox 比例风险回归来关联多基因风险评分的五分位数与静脉血栓栓塞的发生率。

结果

在中位 26 年的随访期间,476 名参与者发生了静脉血栓栓塞事件。冠状动脉疾病多基因风险评分与静脉血栓栓塞事件之间似乎没有明显的关联,年龄、性别、体重指数调整后的风险比在五分位数中分别为 1(参照)、0.87(0.65,1.15)、1.08(0.82,1.42)、0.96(0.72,1.27)和 1.03(0.78,1.37)。

结论

在这项前瞻性研究中,冠状动脉疾病的遗传易感性并未增加静脉血栓栓塞的风险。

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