Cardiovascular Medicine, University of Bologna, Italy.
Thromb Res. 2012 Mar;129(3):225-9. doi: 10.1016/j.thromres.2011.10.036. Epub 2011 Nov 25.
Although the efficacy of antiplatelet therapy is supported by numerous studies areas of uncertainty and doubt persist both in secondary and in primary prevention. In both settings it can be surmised that, with few exceptions, the relative risk reduction obtained, for instance, with aspirin, is rather uniform across the different clinical conditions and measures "efficacy" of the drug: while the absolute risk reduction varies according to the risk levels of the different conditions, and expresses the "efficiency" of the treatment. Especially in conditions at high risk as the acute coronary syndrome (ACS) the problem of "variability of response" or "resistance" to antiaggregating drugs is of remarkable importance. For aspirin resistance main factors are low compliance, interferences with other drugs, especially NSAIDS, diabetes and related glication phenomenon, and especially fast platelet turnover. Genetic polymorphism (C50T) of COX1 gene, has been described but its significance is debated. Regarding clopidogrel, drug interferences, diabetes mellitus, increased platelet turnover, and polymorphisms of the cytochrome P450 family are involved. A useful expression of antiplatelet resistance is "High on Treatment Platelet Reactivity" (HTPR). This entity has been found predictive of poor outcome in a number of studies of patients with ACS, but not in all. Similarly, genotyping patients for cytochrome P450 polymorphisms also shows predictivity, but not confirmed in all studies. Both genotyping and measuring HTPR can be useful for selection of high risk ACS patients and especially in clinical research. New antiplatelet drugs as prasugrel, ticagrelor, and the recent vorapaxar seem to overcome the problem of resistance. In primary prevention, even assuming a uniform efficacy of aspirin, the risk and hence the absolute number of events spared are much lower. Therefore, aspirin will be less efficient, and the net clinical benefit over the bleeding risk will be smaller. Inconclusive results have been found in healthy people as well as in people with diabetes but no prior cardiovascular event. However, in a recent meta-analysis including new trials bearing some factors of heterogeneity, a small but significant reduction in overall mortality suggests that, for aspirin in primary prevention, "the game is not over".
虽然抗血小板治疗的疗效得到了众多研究的支持,但在二级和一级预防中仍然存在不确定性和疑虑。在这两种情况下,可以推测,除了少数例外,例如,阿司匹林获得的相对风险降低在不同的临床情况下相当一致,这是药物的“疗效”:而绝对风险降低则根据不同情况下的风险水平而变化,表达了治疗的“效率”。特别是在急性冠状动脉综合征(ACS)等高危情况下,抗聚集药物的“反应变异性”或“耐药性”问题非常重要。对于阿司匹林耐药,主要因素是低依从性、与其他药物的相互作用,尤其是 NSAIDs、糖尿病和相关的糖基化现象,尤其是血小板快速更新。COX1 基因的遗传多态性(C50T)已经被描述,但它的意义仍存在争议。至于氯吡格雷,药物相互作用、糖尿病、血小板更新增加和细胞色素 P450 家族的多态性都与之相关。抗血小板抵抗的一个有用的表达方式是“治疗中的高血小板反应性”(HTPR)。在一些 ACS 患者的研究中,这种实体已被发现对预后不良具有预测性,但并非所有研究都如此。同样,对细胞色素 P450 多态性进行基因分型的患者也显示出预测性,但并非所有研究都得到证实。基因分型和测量 HTPR 都可以用于选择高危 ACS 患者,特别是在临床研究中。新型抗血小板药物如普拉格雷、替格瑞洛和最近的沃拉帕沙似乎克服了耐药性问题。在一级预防中,即使假设阿司匹林的疗效一致,风险也因此而避免的事件绝对数量要低得多。因此,阿司匹林的效率将更低,出血风险的净临床获益将更小。在健康人群和无心血管事件的糖尿病患者中,也得出了不确定的结果。然而,在一项包括一些异质性因素的新试验的荟萃分析中,发现总死亡率略有降低,这表明在一级预防中,阿司匹林的“游戏还没有结束”。