Amici Serena, Paciaroni Maurizio, Agnelli Giancarlo, Caso Valeria
Stroke Unit, Division of Cardiovascular Medicine, University of Perugia, Santa Maria della Misericordia Hospital, Sant'Andrea delle Fratte, 06126 Perugia, Italy.
Stroke Res Treat. 2011;2011:212485. doi: 10.4061/2011/212485. Epub 2011 Nov 10.
Stroke is the third cause of mortality and one of most frequent causes of long-term neurological disability, as well as a complex disease that results from the interaction of environmental and genetic factors. The focus on genetics has produced a large number of studies with the objective of revealing the genetic basis of cerebrovascular diseases. Furthermore, pharmacogenetic research has investigated the relation between genetic variability and drug effectiveness/toxicity. This review will examine the implications of pharmacogenetics of stroke; data on antihypertensives, statins, antiplatelets, anticoagulants, and recombinant tissue plasminogen activator will be illustrated. Several polymorphisms have been studied and some have been associated with positive drug-gene interaction on stroke, but the superiority of the genotype-guided approach over the clinical approach has not been proved yet; for this reason, it is not routinely recommended.
中风是导致死亡的第三大原因,也是长期神经功能残疾最常见的原因之一,它是一种由环境因素和遗传因素相互作用导致的复杂疾病。对遗传学的关注催生了大量旨在揭示脑血管疾病遗传基础的研究。此外,药物遗传学研究探讨了基因变异性与药物疗效/毒性之间的关系。本综述将探讨中风药物遗传学的意义;将举例说明有关抗高血压药、他汀类药物、抗血小板药、抗凝药和重组组织型纤溶酶原激活剂的数据。已经对几种多态性进行了研究,其中一些与中风的药物-基因阳性相互作用有关,但基因型指导方法相对于临床方法的优越性尚未得到证实;因此,不常规推荐这种方法。