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Vascular risk levels affect the predictive value of platelet reactivity for the occurrence of MACE in patients on clopidogrel. Systematic review and meta-analysis of individual patient data

机译:血管风险水平影响氯吡格雷患者发生MACE时血小板反应性的预测价值。个别患者数据的系统审查和荟萃分析

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摘要

Prior studies have shown an association between high on-clopidogrel platelet reactivity (PR) and the risk of major adverse cardiovascular events (MACE). However, large intervention trials on PR-tailored treatments have been neutral. The role and usefulness of PR with regard to levels of cardiovascular risk are unclear. We undertook a systematic review and meta-analysis of individual patient data on MACE outcomes (acute coronary syndromes (ACS), ischaemic strokes, and vascular deaths) in relation to PR and its interaction with cardiovascular risk levels. PR was determined using ADP-induced light transmission aggregometry with a primary concentration of 20 µM ADP. Thirteen prospective studies totaled 6,478 clopidogrel-treated patients who experienced 421 MACE (6.5 %) during a median follow-up of 12 months. The strength of the association between the risk of MACE and PR increased significantly (p=0.04) with the number of risk factors present (age> 75 years, ACS at inclusion, diabetes, and hypertension). No association was detected in patients with no risk factor (p=0.48). In patients presenting one risk factor, only high-PR was associated with an increased risk of MACE (HR 3.2, p=0.001). In patients presenting ≥ 2 risk factors, the increase of risk started from medium-PR (medium-PR: HR=2.9, p=0.0004; high-PR: HR=3.7, p=0.0003). PR allowed the reclassification of 44 % of the total population to a different risk level for the outcome of MACE, mostly in intermediate or high risk patients. In conclusion, the magnitude of the association between PR and MACE risk is strongly dependent on the level of cardiovascular risk faced by patients on clopidogrel.
机译:先前的研究表明,高氯吡格雷血小板反应性(PR)与重大不良心血管事件(MACE)的风险之间存在关联。但是,针对PR量身定制的治疗方法的大型干预试验是中立的。 PR在心血管风险水平方面的作用和用途尚不清楚。我们对与PR相关的MACE结果(急性冠脉综合征(ACS),缺血性中风和血管死亡)进行了系统的回顾和荟萃分析,以了解其MACE结局及其与心血管疾病风险水平的相互作用。 PR是使用ADP诱导的光聚集法测定的,主要浓度为20 µM ADP。 13项前瞻性研究总计对6478例接受氯吡格雷治疗的患者进行了12个月的中位随访,其中有421例MACE(6.5 %%)。 MACE和PR的风险之间的关联强度随着存在的风险因素的数量(年龄> 75岁,纳入时ACS,糖尿病和高血压)而显着增加(p = 0.04)。没有危险因素的患者中未发现相关性(p = 0.48)。在表现出一种危险因素的患者中,只有高PR与MACE风险增加相关(HR 3.2,p = 0.001)。在存在≥2个危险因素的患者中,危险性的增加始于中PR(中PR:HR = 2.9,p = 0.0004;高PR:HR = 3.7,p = 0.0003)。 PR使总人口的44%重新分类为MACE结局的不同风险水平,主要是中级或高风险患者。总之,PR和MACE风险之间的关联程度在很大程度上取决于氯吡格雷患者所面临的心血管风险水平。
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