Metabolic Signatures of Blood Pressure and Risk of Cardiovascular Diseases.

IF 5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Maria Manou, Christos Papagiannopoulos, Christos V Chalitsios, Alexandros-Georgios Asimakopoulos, Georgios Markozannes, Monica Bulló, Konstantinos K Tsilidis, Christopher Papandreou, Ioanna Tzoulaki
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Abstract

Background: The underlying biological mechanisms linking blood pressure (BP) and cardiovascular diseases (CVD) are only partly understood. We aimed to identify metabolic signatures associated with systolic and diastolic BP and investigate their subsequent association with risk of CVD.

Methods and results: The study included 201 742 UK Biobank participants with measurements on 249 metabolic biomarkers. A multistep adaptive elastic net penalized regression with 10-fold cross-validation was employed to identify metabolic signatures for systolic BP and diastolic BP. External validation was conducted on 848 participants from the EHS (Epirus Health Study). We further assessed the associations between BP metabolic signatures and incident composite CVD (N=6742), myocardial infarction (N=4192), and stroke (N=2757) in the UK Biobank, using multivariable Cox regression models. The metabolic signatures comprised 31 and 25 metabolites, robustly correlated with systolic BP and diastolic BP, respectively, in both the UK Biobank and the EHS. Following adjustments (including BP), the metabolic signature for systolic BP was positively associated with incident myocardial infarction (hazard ratio [HR], 1.11 [95% CI, 1.07-1.15]) and CVD (HR, 1.07 [95% CI, 1.04-1.10]). Similarly, the metabolic signature for diastolic BP was associated with a higher risk of myocardial infarction (HR, 1.16 [95% CI, 1.12-1.20]) and CVD (HR, 1.09 [95% CI, 1.05-1.12]). The associations between the signatures and stroke were not significant. The metabolic signatures partly mediated the total effect of the BP traits on the risk of myocardial infarction and CVD.

Conclusions: Our findings may enhance our understanding of the biological mechanisms through which BP affects CVD.

血压与心血管疾病风险的代谢特征
背景:人们对血压(BP)与心血管疾病(CVD)之间的潜在生物学机制仅有部分了解。我们旨在确定与收缩压和舒张压相关的代谢特征,并研究它们与心血管疾病风险的后续关联:研究纳入了 201 742 名英国生物库参与者,对 249 种代谢生物标志物进行了测量。采用多步自适应弹性网惩罚回归和 10 倍交叉验证来识别收缩压和舒张压的代谢特征。外部验证在伊庇鲁斯健康研究(EHS)的 848 名参与者中进行。我们使用多变量 Cox 回归模型进一步评估了英国生物库中血压代谢特征与心血管疾病(6742 例)、心肌梗死(4192 例)和中风(2757 例)发病率之间的关系。代谢特征包括 31 和 25 个代谢物,分别与英国生物库和 EHS 的收缩压和舒张压密切相关。经过调整(包括血压)后,收缩压的代谢特征与心肌梗死事件(危险比 [HR],1.11 [95% CI,1.07-1.15])和心血管疾病(HR,1.07 [95% CI,1.04-1.10])呈正相关。同样,舒张压的代谢特征与较高的心肌梗死风险(HR,1.16 [95% CI,1.12-1.20])和心血管疾病风险(HR,1.09 [95% CI,1.05-1.12])相关。这些特征与中风之间的关系并不显著。代谢特征部分介导了血压特征对心肌梗死和心血管疾病风险的总体影响:我们的研究结果可能会加深我们对血压影响心血管疾病的生物学机制的理解。
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来源期刊
Journal of the American Heart Association
Journal of the American Heart Association CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
9.40
自引率
1.90%
发文量
1749
审稿时长
12 weeks
期刊介绍: As an Open Access journal, JAHA - Journal of the American Heart Association is rapidly and freely available, accelerating the translation of strong science into effective practice. JAHA is an authoritative, peer-reviewed Open Access journal focusing on cardiovascular and cerebrovascular disease. JAHA provides a global forum for basic and clinical research and timely reviews on cardiovascular disease and stroke. As an Open Access journal, its content is free on publication to read, download, and share, accelerating the translation of strong science into effective practice.
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