Zineh Issam
University of Florida College of Pharmacy, Department of Pharmacy Practice and Center for Pharmacogenomics, Gainesville, FL 32610, USA.
Curr Atheroscler Rep. 2007 Sep;9(3):187-94. doi: 10.1007/s11883-007-0018-3.
The 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase inhibitors (statins) are among the most commonly prescribed drugs worldwide. On average, statins improve lipid profiles and have been shown to have ancillary beneficial effects on inflammation, platelet activity, and endothelial function. However, variability in drug response exists regardless of the measured phenotype, and genetic variability may be a contributing factor. Recently, there has been an interesting shift in statin pharmacogenetic studies. Novel study designs have been employed and nontraditional candidate genes have been investigated in relation to both lipid and nonlipid responses to statins. This review outlines earlier pharmacogenetic studies and highlights newly published findings that expand on previous work. Furthermore, a framework is provided in which the necessary next steps in research are described, with the ultimate goal of translating pharmacogenetic findings into clinically meaningful changes in patient care.
3-羟基-3-甲基戊二酰辅酶A(HMG CoA)还原酶抑制剂(他汀类药物)是全球最常用的处方药之一。平均而言,他汀类药物可改善血脂水平,并已显示出对炎症、血小板活性和内皮功能具有辅助有益作用。然而,无论所测量的表型如何,药物反应都存在变异性,遗传变异性可能是一个促成因素。最近,他汀类药物的药物遗传学研究出现了一个有趣的转变。采用了新的研究设计,并针对他汀类药物的脂质和非脂质反应研究了非传统候选基因。本综述概述了早期的药物遗传学研究,并强调了在先前工作基础上扩展的新发表的研究结果。此外,还提供了一个框架,其中描述了研究中必要的后续步骤,最终目标是将药物遗传学研究结果转化为患者护理中具有临床意义的变化。