Department of Pharmacotherapy and Translational Research and Center for Pharmacogenomics, University of Florida College of Pharmacy, Gainesville, FL.
College of Medicine, University of Florida, Gainesville, FL.
J Am Heart Assoc. 2017 Nov 2;6(11):e006522. doi: 10.1161/JAHA.117.006522.
The majority of hypertensive individuals require combination antihypertensive therapy to achieve adequate blood pressure (BP) control. This study aimed to identify genetic variants associated with uncontrolled BP on combination therapy with a thiazide diuretic and a β-blocker.
A genome-wide association study of uncontrolled BP on combination therapy was conducted among 314 white participants of the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) trial. Multivariable logistic regression analysis was used. Genetic variants meeting a suggestive level of significance (<1.0E-05) were tested for replication in an external cohort, INVEST (International Verapamil-SR Trandolapril study). We also examined genome-wide variant associations with systolic and diastolic BP response on combination therapy and tested for replication. We discovered a single nucleotide polymorphism, the rs261316 major allele, at chromosome 15 in the gene associated with an increased odds of having uncontrolled BP on combination therapy (odds ratio: 2.56, 95% confidence interval, 1.69-3.88, =8.64E-06). This single nucleotide polymorphism replicated (odds ratio: 1.86, 95% confidence interval, 1.35-2.57, =0.001) and approached genome-wide significance in the meta-analysis between discovery and replication cohorts (odds ratio: 2.16, 95% confidence interval, 1.63-2.86, =8.60E-08). Other genes in the region surrounding rs261316 ( include and .
A single nucleotide polymorphism in the gene may be associated with uncontrolled BP following treatment with a thiazide diuretic/β-blocker combination.
URL: https://www.clinicaltrials.gov. Unique identifier: NCT00246519.
大多数高血压患者需要联合降压治疗才能达到足够的血压(BP)控制。本研究旨在确定与噻嗪类利尿剂和β受体阻滞剂联合治疗时血压控制不佳相关的遗传变异。
对 PEAR(降压反应的药物基因组学评估)试验的 314 名白种参与者进行了联合治疗时血压控制不佳的全基因组关联研究。采用多变量逻辑回归分析。对达到提示水平显著性(<1.0E-05)的遗传变异进行了外部队列 INVEST(国际维拉帕米-SR 曲多普利研究)的复制检验。我们还检查了全基因组变异与联合治疗时收缩压和舒张压反应的关联,并进行了复制检验。我们发现了一个单核苷酸多态性,即染色体 15 上基因中的 rs261316 主要等位基因,与联合治疗时血压控制不佳的几率增加相关(比值比:2.56,95%置信区间,1.69-3.88,=8.64E-06)。这个单核苷酸多态性在发现和复制队列的荟萃分析中复制(比值比:1.86,95%置信区间,1.35-2.57,=0.001),并接近全基因组显著性(比值比:2.16,95%置信区间,1.63-2.86,=8.60E-08)。rs261316 周围区域的其他基因(包括 和 。
基因中的一个单核苷酸多态性可能与噻嗪类利尿剂/β受体阻滞剂联合治疗后血压控制不佳有关。