Ridker Paul M
From the Center for Cardiovascular Disease Prevention, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Circ Res. 2016 Jan 8;118(1):145-56. doi: 10.1161/CIRCRESAHA.115.306656.
Plasma levels of the inflammatory biomarker high-sensitivity C-reactive protein (hsCRP) predict vascular risk with an effect estimate as large as that of total or high-density lipoprotein cholesterol. Further, randomized trial data addressing hsCRP have been central to understanding the anti-inflammatory effects of statin therapy and have consistently demonstrated on-treatment hsCRP levels to be as powerful a predictor of residual cardiovascular risk as on-treatment levels of low-density lipoprotein cholesterol. Yet, although hsCRP is clinically useful as a biomarker for risk prediction, most mechanistic studies suggest that CRP itself is unlikely to be a target for intervention. Moving upstream in the inflammatory cascade from CRP to interleukin (IL)-6 to IL-1 provides novel therapeutic opportunities for atheroprotection that focus on the central IL-6 signaling system and ultimately on inhibition of the IL-1β-producing NOD-like receptor family pyrin domain containing 3 inflammasome. Cholesterol crystals, neutrophil extracellular traps, atheroprone flow, and local tissue hypoxia activate the NOD-like receptor family pyrin domain containing 3 inflammasome. As such, a unifying concept of hsCRP as a downstream surrogate biomarker for upstream IL-1β activity has emerged. From a therapeutic perspective, small ischemia studies show reductions in acute-phase hsCRP production with the IL-1 receptor antagonist anakinra and the IL-6 receptor blocker tocilizumab. A phase IIb study conducted among diabetic patients at high vascular risk indicates that canakinumab, a human monoclonal antibody that targets IL-1β, markedly reduces plasma levels of IL-6, hsCRP, and fibrinogen with little change in atherogenic lipids. Canakinumab in now being tested as a method to prevent recurrent cardiovascular events in a randomized trial of 10 065 post-myocardial infarction patients with elevated hsCRP that is fully enrolled and due to complete in 2017. Clinical trials using alternative anti-inflammatory agents active against the CRP/IL-6/IL-1 axis, including low-dose methotrexate and colchicine, are being explored. If successful, these trials will close the loop on the inflammatory hypothesis of atherosclerosis and serve as examples of how fundamental biologic principles can be translated into personalized medical practice.
炎症生物标志物高敏C反应蛋白(hsCRP)的血浆水平可预测血管风险,其效应估计值与总胆固醇或高密度脂蛋白胆固醇的效应估计值一样大。此外,针对hsCRP的随机试验数据对于理解他汀类药物治疗的抗炎作用至关重要,并且一致表明治疗期间的hsCRP水平与治疗期间低密度脂蛋白胆固醇水平一样,都是残余心血管风险的有力预测指标。然而,尽管hsCRP作为风险预测的生物标志物在临床上很有用,但大多数机制研究表明,CRP本身不太可能成为干预靶点。从炎症级联反应的上游从CRP到白细胞介素(IL)-6再到IL-1,为动脉粥样硬化保护提供了新的治疗机会,这些机会聚焦于核心的IL-6信号系统,并最终聚焦于抑制产生IL-1β的含NOD样受体家族吡啉结构域3的炎性小体。胆固醇晶体、中性粒细胞胞外陷阱、易致动脉粥样硬化的血流和局部组织缺氧会激活含NOD样受体家族吡啉结构域3的炎性小体。因此,已经出现了一个将hsCRP作为上游IL-1β活性的下游替代生物标志物的统一概念。从治疗角度来看,小型缺血研究表明,使用IL-1受体拮抗剂阿那白滞素和IL-6受体阻滞剂托珠单抗可降低急性期hsCRP的产生。在高血管风险的糖尿病患者中进行的一项IIb期研究表明,靶向IL-1β的人单克隆抗体卡那单抗可显著降低血浆IL-6、hsCRP和纤维蛋白原水平,而致动脉粥样硬化脂质变化不大。卡那单抗目前正在一项针对10065例hsCRP升高的心肌梗死后患者的随机试验中作为预防心血管事件复发的方法进行测试,该试验已完全入组,预计2017年完成。正在探索使用对CRP/IL-6/IL-1轴有活性的其他抗炎药物进行临床试验,包括低剂量甲氨蝶呤和秋水仙碱。如果成功,这些试验将完善动脉粥样硬化的炎症假说,并成为将基本生物学原理转化为个性化医疗实践的范例。