Mehanna Mai, McDonough Caitrin W, Smith Steven M, Gong Yan, Gums John G, Chapman Arlene B, Johnson Julie A, McIntyre Lauren, Cooper-DeHoff Rhonda M
Department of Pharmacotherapy and Translational Research and Center for Pharmacogenomics and Precision Medicine, College of Pharmacy, University of Florida, Gainesville, FL 32610, USA.
Department of Medicine, University of Chicago, Chicago, IL 60637, USA.
Metabolites. 2021 Sep 21;11(9):645. doi: 10.3390/metabo11090645.
Plasma renin activity (PRA) is a predictive biomarker of blood pressure (BP) response to antihypertensives in European-American hypertensive patients. We aimed to identify the metabolic signatures of baseline PRA and the linkages with BP response to β-blockers and thiazides. Using data from the Pharmacogenomic Evaluation of Antihypertensive Responses-2 (PEAR-2) trial, multivariable linear regression adjusting for age, sex and baseline systolic-BP (SBP) was performed on European-American individuals treated with metoprolol ( = 198) and chlorthalidone ( = 181), to test associations between 856 metabolites and baseline PRA. Metabolites with a false discovery rate (FDR) < 0.05 or < 0.01 were tested for replication in 463 European-American individuals treated with atenolol or hydrochlorothiazide. Replicated metabolites were then tested for validation based on the directionality of association with BP response. Sixty-three metabolites were associated with baseline PRA, of which nine, including six lipids, were replicated. Of those replicated, two metabolites associated with higher baseline PRA were validated: caprate was associated with greater metoprolol SBP response (β = -1.7 ± 0.6, = 0.006) and sphingosine-1-phosphate was associated with reduced hydrochlorothiazide SBP response (β = 7.6 ± 2.8, = 0.007). These metabolites are clustered with metabolites involved in sphingolipid, phospholipid, and purine metabolic pathways. The identified metabolic signatures provide insights into the mechanisms underlying BP response.
血浆肾素活性(PRA)是欧美高血压患者血压(BP)对抗高血压药物反应的预测生物标志物。我们旨在确定基线PRA的代谢特征以及与β受体阻滞剂和噻嗪类药物血压反应的联系。利用抗高血压反应的药物基因组学评估-2(PEAR-2)试验的数据,对接受美托洛尔(n = 198)和氯噻酮(n = 181)治疗的欧美个体进行多变量线性回归,调整年龄、性别和基线收缩压(SBP),以测试856种代谢物与基线PRA之间的关联。对错误发现率(FDR)<0.05或P<0.01的代谢物在463名接受阿替洛尔或氢氯噻嗪治疗的欧美个体中进行重复验证。然后根据与血压反应的关联方向对重复验证的代谢物进行验证。63种代谢物与基线PRA相关,其中9种包括6种脂质被重复验证。在这些被重复验证的代谢物中,两种与较高基线PRA相关的代谢物得到验证:癸酸盐与美托洛尔SBP反应增强相关(β=-1.7±0.6,P = 0.006),鞘氨醇-1-磷酸与氢氯噻嗪SBP反应降低相关(β = 7.6±2.8,P = 0.007)。这些代谢物与参与鞘脂、磷脂和嘌呤代谢途径的代谢物聚集在一起。所确定的代谢特征为血压反应的潜在机制提供了见解。