Am J Epidemiol. 2021 Oct 1;190(10):2000-2014. doi: 10.1093/aje/kwab031.
Cardiovascular disease (CVD) risk-prediction models are used to identify high-risk individuals and guide statin initiation. However, these models are usually derived from individuals who might initiate statins during follow-up. We present a simple approach to address statin initiation to predict "statin-naive" CVD risk. We analyzed primary care data (2004-2017) from the UK Clinical Practice Research Datalink for 1,678,727 individuals (aged 40-85 years) without CVD or statin treatment history at study entry. We derived age- and sex-specific prediction models including conventional risk factors and a time-dependent effect of statin initiation constrained to 25% risk reduction (from trial results). We compared predictive performance and measures of public-health impact (e.g., number needed to screen to prevent 1 event) against models ignoring statin initiation. During a median follow-up of 8.9 years, 103,163 individuals developed CVD. In models accounting for (versus ignoring) statin initiation, 10-year CVD risk predictions were slightly higher; predictive performance was moderately improved. However, few individuals were reclassified to a high-risk threshold, resulting in negligible improvements in number needed to screen to prevent 1 event. In conclusion, incorporating statin effects from trial results into risk-prediction models enables statin-naive CVD risk estimation and provides moderate gains in predictive ability but had a limited impact on treatment decision-making under current guidelines in this population.
心血管疾病 (CVD) 风险预测模型用于识别高危个体并指导他汀类药物的起始使用。然而,这些模型通常是基于随访期间可能开始使用他汀类药物的个体推导得出的。我们提出了一种简单的方法来解决他汀类药物起始使用的问题,以预测“他汀类药物初治”的 CVD 风险。我们分析了来自英国临床实践研究数据链的初级保健数据(2004-2017 年),该数据来自 1678727 名无 CVD 或他汀类药物治疗史的个体(年龄 40-85 岁)。我们推导出了年龄和性别特异性预测模型,包括常规风险因素和他汀类药物起始的时间依赖性效应,限制为降低 25%的风险(来自试验结果)。我们比较了不考虑他汀类药物起始使用的模型的预测性能和公共卫生影响指标(例如,预防 1 次事件所需的筛查人数)。在中位随访 8.9 年期间,有 103163 名患者发生了 CVD。在考虑(与忽略)他汀类药物起始使用的模型中,10 年 CVD 风险预测值略高;预测性能得到适度改善。然而,只有少数个体被重新分类为高风险阈值,导致预防 1 次事件所需的筛查人数几乎没有改善。总之,将试验结果中的他汀类药物效果纳入风险预测模型可实现他汀类药物初治 CVD 风险估计,并适度提高预测能力,但在当前指南下对该人群的治疗决策影响有限。