Lynch Amy I, Irvin Marguerite R, Davis Barry R, Ford Charles E, Eckfeldt John H, Arnett Donna K
Department of Epidemiology, University of Alabama at Birmingham, RPHB 220E, 1530 3rd Avenue South, Birmingham, AL 55294-0022, USA.
Int J Hypertens. 2013;2013:578578. doi: 10.1155/2013/578578. Epub 2013 Oct 31.
Treatment resistant hypertension (TRH) is defined as uncontrolled hypertension (HTN) despite the use of ≥3 antihypertensive medication classes or controlled HTN while treated with ≥4 antihypertensive medication classes. Risk factors for TRH include increasing age, diminished kidney function, higher body mass index, diabetes, and African American (AA) race. Importantly, previous studies suggest a genetic role in TRH, although the genetics of TRH are largely understudied. With 2203 treatment resistant cases and 2354 treatment responsive controls (36% AA) from the Genetics of Hypertension Associated Treatment Study (GenHAT), we assessed the association of 78 candidate gene polymorphisms with TRH status using logistic regression. After stratifying by race and adjusting for potential confounders, there were 2 genetic variants in the AGT gene (rs699, rs5051) statistically significantly associated with TRH among white participants. The Met allele of rs699 and the G allele of rs5051 were positively associated with TRH: OR = 1.27 (1.12-1.44), P = 0.0001, and OR = 1.36 (1.20-1.53), P < 0.0001, respectively. There was no similar association among AA participants (race interaction P = 0.0004 for rs699 and P = 0.0001 for rs5051). This research contributes to our understanding of the genetic basis of TRH, and further genetic studies of TRH may help reach the goal of better clinical outcomes for hypertensive patients.
难治性高血压(TRH)的定义为,尽管使用了≥3类抗高血压药物但高血压仍未得到控制,或在使用≥4类抗高血压药物治疗时高血压得到控制。TRH的危险因素包括年龄增长、肾功能减退、体重指数较高、糖尿病以及非裔美国人(AA)种族。重要的是,既往研究表明基因在TRH中发挥作用,尽管TRH的遗传学在很大程度上尚未得到充分研究。利用高血压相关治疗遗传学研究(GenHAT)中的2203例难治性病例和2354例治疗反应性对照(36%为AA种族),我们采用逻辑回归评估了78个候选基因多态性与TRH状态的关联。在按种族分层并对潜在混杂因素进行校正后,AGT基因中的2个基因变异(rs699、rs5051)在白人参与者中与TRH存在统计学显著关联。rs699的Met等位基因和rs5051的G等位基因与TRH呈正相关:OR分别为1.27(1.12 - 1.44),P = 0.0001,以及OR为1.36(1.20 - 1.53),P < 0.0001。在AA参与者中未观察到类似关联(rs699的种族交互作用P = 0.0004,rs5051的种族交互作用P = 0.0001)。这项研究有助于我们理解TRH的遗传基础,TRH的进一步遗传学研究可能有助于实现改善高血压患者临床结局的目标。