Department of Medicine, Division of Preventive Medicine and Epidemiology, Boston University School of Medicine, Boston, Massachusetts 02119, USA.
Clin Cardiol. 2013 Jan;36(1):15-20. doi: 10.1002/clc.22046. Epub 2012 Aug 9.
Given the results of the Justification for the Use of Statins in Primary Prevention: An Intervention Trial Evaluating Rosuvastatin (JUPITER) trial, statin initiation may be considered for individuals with elevated high-sensitivity C-reactive protein (hsCRP). However, if followed prospectively, many individuals with elevated CRP may become statin eligible, limiting the impact of elevated CRP as a treatment indication. This analysis estimates the proportion of people with elevated CRP that become statin eligible over time.
Most people with elevated CRP become statin eligible over a short period of time.
We followed 2153 Multi-Ethnic Study of Atherosclerosis (MESA) participants free of cardiovascular disease and diabetes with low-density lipoprotein cholesterol <130 mg/dL at baseline to determine the proportion who become eligible for statins over 4.5 years. The proportion eligible for statin therapy, defined by the National Cholesterol Education Program (NCEP) 2004 updated guidelines, was calculated at baseline and during follow-up stratified by baseline CRP level (≥2 mg/L).
At baseline, 47% of the 2153 participants had elevated CRP. Among participants with elevated CRP, 29% met NCEP criteria for statins, compared with 28% without elevated CRP at baseline. By 1.5 years later, 26% and 22% (P = 0.09) of those with and without elevated CRP at baseline reached NCEP low-density lipoprotein cholesterol criteria and/or had started statins, respectively. These increased to 42% and 39% (P = 0.24) at 3 years and 59% and 52% (P = 0.01) at 4.5 years following baseline.
A substantial proportion of those with elevated CRP did not achieve NCEP-based statin eligibility over 4.5 years of follow-up. These findings suggest that many patients with elevated CRP may not receive the benefits of statins if CRP is not incorporated into the NCEP screening strategy.
鉴于“他汀类药物在一级预防中的应用理由:评估瑞舒伐他汀的干预试验(JUPITER)”试验的结果,对于高敏 C 反应蛋白(hsCRP)升高的个体,可能会考虑开始使用他汀类药物。然而,如果进行前瞻性随访,许多 CRP 升高的个体可能会符合他汀类药物治疗标准,从而限制 CRP 升高作为治疗指标的影响。本分析估计随着时间的推移,hsCRP 升高的人群中符合他汀类药物治疗标准的比例。
大多数 CRP 升高的人在短时间内会符合他汀类药物治疗标准。
我们对 2153 名无心血管疾病和糖尿病且基线时 LDL 胆固醇<130mg/dL 的多民族动脉粥样硬化研究(MESA)参与者进行了随访,以确定在 4.5 年内有多少人符合他汀类药物治疗标准。根据国家胆固醇教育计划(NCEP)2004 年更新的指南,定义了他汀类药物治疗的标准(NCEP 标准),并在基线和随访期间根据基线 CRP 水平(≥2mg/L)进行分层。
在基线时,2153 名参与者中有 47%的 CRP 升高。在 CRP 升高的参与者中,有 29%符合 NCEP 标准,而基线时 CRP 不升高的参与者中这一比例为 28%。在 1.5 年后,基线时 CRP 升高和不升高的参与者中,分别有 26%和 22%(P=0.09)达到了 NCEP 低密度脂蛋白胆固醇标准和/或开始服用他汀类药物。这一比例在 3 年时分别增加到 42%和 39%(P=0.24),在 4.5 年时分别增加到 59%和 52%(P=0.01)。
在 4.5 年的随访中,有相当一部分 CRP 升高的人未达到 NCEP 标准的他汀类药物治疗标准。这些发现表明,如果 CRP 未纳入 NCEP 筛查策略,许多 CRP 升高的患者可能无法从他汀类药物治疗中获益。