Do A N, Lynch A I, Claas S A, Boerwinkle E, Davis B R, Ford C E, Eckfeldt J H, Tiwari H K, Arnett D K, Irvin M R
Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
Human Genetics Center, University of Texas Health Science Center at Houston, Houston, TX, USA.
J Hum Hypertens. 2016 Sep;30(9):549-54. doi: 10.1038/jhh.2015.121. Epub 2016 Jan 21.
African Americans have the highest prevalence of hypertension in the United States. Blood pressure (BP) control is important to reduce cardiovascular disease-related morbidity and mortality in this ethnic group. Genetic variants have been found to be associated with BP response to treatment. Previous pharmacogenetic studies of BP response to treatment in African Americans suffer limitations of small sample size as well as a limited number of candidate genes, and often focused on one antihypertensive treatment. Using 1131 African-American treatment-naive participants from the Genetics of Hypertension Associated Treatment Study, we examined whether variants in 35 candidate genes might modulate BP response to four different antihypertensive medications, including an angiotensin-converting enzyme inhibitor (lisinopril), a calcium channel blocker (amlodipine), and an a-adrenergic blocker (doxazosin) as compared with a thiazide diuretic (chlorthalidone) after 6 months of follow-up. Several suggestive gene by treatment interactions were identified. For example, among participants with two minor alleles of renin rs6681776, diastolic BP response was much improved on doxazosin compared with chlorthalidone (on average -9.49 mm Hg vs -1.70 mm Hg) (P=0.007). Although several suggestive loci were identified, none of the findings passed significance criteria after correction for multiple testing. Given the impact of hypertension and its sequelae in this population, this research highlights the potential for genetic factors to contribute to BP response to treatment. Continued concerted research efforts focused on genetics are needed to improve treatment response in this high-risk group.
非裔美国人在美国高血压患病率最高。血压控制对于降低该种族群体中心血管疾病相关的发病率和死亡率至关重要。已发现基因变异与血压对治疗的反应有关。先前针对非裔美国人血压对治疗反应的药物遗传学研究存在样本量小以及候选基因数量有限的局限性,并且通常只关注一种抗高血压治疗。我们利用来自高血压相关治疗遗传学研究的1131名未接受过治疗的非裔美国参与者,研究了35个候选基因的变异是否可能调节血压对四种不同抗高血压药物的反应,这四种药物包括一种血管紧张素转换酶抑制剂(赖诺普利)、一种钙通道阻滞剂(氨氯地平)、一种α-肾上腺素能阻滞剂(多沙唑嗪),并与一种噻嗪类利尿剂(氯噻酮)进行比较,随访6个月后观察效果。我们识别出了一些提示性的基因与治疗的相互作用。例如,在具有肾素rs6681776两个次要等位基因的参与者中,与氯噻酮相比,多沙唑嗪使舒张压反应有显著改善(平均-9.49 mmHg对-1.70 mmHg)(P = 0.007)。尽管识别出了一些提示性位点,但在进行多重检验校正后,没有一项发现达到显著性标准。鉴于高血压及其后遗症对该人群的影响,这项研究凸显了遗传因素对血压治疗反应产生影响的可能性。需要继续集中开展针对遗传学的协同研究工作,以改善这个高危群体的治疗反应。