首页> 美国卫生研究院文献>Springer Open Choice >Do Genetic Variants of the Renin-Angiotensin System Predict Blood Pressure Response to Renin-Angiotensin System–Blocking Drugs? A Systematic Review of Pharmacogenomics in the Renin-Angiotensin System
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Do Genetic Variants of the Renin-Angiotensin System Predict Blood Pressure Response to Renin-Angiotensin System–Blocking Drugs? A Systematic Review of Pharmacogenomics in the Renin-Angiotensin System

机译:肾素-血管紧张素系统的遗传变异是否可以预测对肾素-血管紧张素系统阻滞药物的血压反应?肾素-血管紧张素系统中药物基因组学的系统评价

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摘要

The concept of “pharmacogenomics” or “pharmacogenetics” promises to offer the ultimate in personalized medicine, and the renin-angiotensin system (RAS) is one of the most plausible candidates for the application of this approach in the area of hypertension. For the past two decades, genetic variants of the RAS have been tested for association with blood pressure response, but the results have been inconsistent. The problems have been attributed to many issues, but the most fundamental concern is thought to be the statistical power of the studies. Therefore, we have tried to put together a new systematic review using a database search including only recent reports with adequate numbers of subjects, and 11 reports were identified. From the results, we were able to draw conclusions with nearly consistent findings that the conventional genetic variants of the system (i.e., the ACE I/D, AGT M235T, AT1 A1166C, and AT2 variant) are not associated with antihypertensive effects by RAS blockade, at least by one individual SNP. By contrast, significant associations have been reported (by one report each) for AGT rs7079, AT1 haplotype, REN, and ACE2. For these variants, further evaluations and confirmation are anticipated.
机译:“药物基因组学”或“药物遗传学”的概念有望提供最终的个性化药物,而肾素-血管紧张素系统(RAS)是在高血压领域应用这种方法的最合理的候选者之一。在过去的二十年中,已经测试了RAS的遗传变异与血压反应的关联,但结果不一致。这些问题归因于许多问题,但最根本的问题被认为是研究的统计能力。因此,我们尝试使用数据库搜索来汇总一个新的系统评价,其中仅包括具有足够主题数的最新报告,并且确定了11个报告。从结果中,我们能够得出几乎一致的结论,即该系统的常规遗传变异体(即ACE I / D,AGT M235T,AT1 A1166C和AT2变异体)与RAS阻断剂与降压作用无关,至少由一个单独的SNP。相比之下,已经报告了AGT rs7079,AT1单倍型,REN和ACE2的显着关联(每个报告一份)。对于这些变体,预计将进行进一步的评估和确认。

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