Suppr超能文献

血清甲状旁腺激素与冠状动脉疾病风险:使用孟德尔随机化探索因果关系。

Serum Parathyroid Hormone and Risk of Coronary Artery Disease: Exploring Causality Using Mendelian Randomization.

机构信息

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

出版信息

J Clin Endocrinol Metab. 2019 Nov 1;104(11):5595-5600. doi: 10.1210/jc.2019-01063.

Abstract

CONTEXT

Elevated circulating parathyroid hormone concentrations have been associated with increased risk of cardiovascular disease in observational studies, but whether the association is causal is unknown.

OBJECTIVE

We used the Mendelian randomization design to test whether genetically increased serum parathyroid hormone (S-PTH) concentrations are associated with coronary artery disease (CAD).

DESIGN, SETTING, AND PARTICIPANTS: Five single-nucleotide polymorphisms robustly associated with S-PTH concentrations were used as instrumental variables to estimate the association of genetically higher S-PTH concentrations with CAD. Summary statistics data for CAD were obtained from a genetic consortium with data from 184,305 individuals (60,801 CAD cases and 123,504 noncases).

MAIN OUTCOME MEASURE

OR of CAD per genetically predicted one SD increase of S-PTH concentrations.

RESULTS

Genetically higher S-PTH concentration was not associated with CAD as a whole or myocardial infarction specifically (∼70% of total cases). The ORs per genetically predicted one SD increase in S-PTH concentration were 1.01 (95% CI: 0.93 to 1.09; P = 0.88) for CAD and 1.02 (95% CI: 0.94 to 1.10; P = 0.64) for myocardial infarction. The lack of association remained in various sensitivity analyses.

CONCLUSION

Genetic predisposition to higher S-PTH concentrations does not appear to be an independent risk factor for CAD.

摘要

背景

在观察性研究中,循环甲状旁腺激素浓度升高与心血管疾病风险增加相关,但这种关联是否具有因果关系尚不清楚。

目的

我们使用孟德尔随机化设计来检验遗传上甲状旁腺激素(S-PTH)浓度升高是否与冠状动脉疾病(CAD)相关。

设计、环境和参与者:使用与 S-PTH 浓度密切相关的五个单核苷酸多态性作为工具变量,以估计遗传上较高的 S-PTH 浓度与 CAD 的相关性。CAD 的汇总统计数据来自一个遗传联盟,该联盟的数据来自 184305 人(60801 例 CAD 病例和 123504 例非病例)。

主要观察指标

CAD 的 OR 每增加一个 S-PTH 浓度的遗传预测标准差。

结果

总体而言,遗传上较高的 S-PTH 浓度与 CAD 或心肌梗死无关(约 70%的总病例)。每增加一个 S-PTH 浓度的遗传预测标准差的 OR 分别为 1.01(95%CI:0.93 至 1.09;P=0.88)用于 CAD 和 1.02(95%CI:0.94 至 1.10;P=0.64)用于心肌梗死。在各种敏感性分析中,缺乏相关性仍然存在。

结论

S-PTH 浓度升高的遗传易感性似乎不是 CAD 的独立危险因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验