Roberts Robert
Heart and Vascular Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, US.
Methodist Debakey Cardiovasc J. 2025 Aug 12;21(4):101-112. doi: 10.14797/mdcvj.1617. eCollection 2025.
Early primary prevention of coronary artery disease (CAD) is limited by lack of biomarkers to detect CAD risk among young asymptomatic individuals. Although early prevention is more effective than secondary interventions, conventional risk factors such as hypertension usually do not appear until the fifth or sixth decade of life. Conversely, genetic risk, which accounts for 50% of all CAD risk, is randomly distributed at conception and does not change with age; therefore, it can be determined any time after birth using a genetic polygenic risk score (PRS). Genetic risk is markedly modified by lifestyle changes and, specifically, lowering levels of low-density lipoproteins (LDL). CAD risk depends on the concentration and duration of exposure to plasma LDL, which is estimated by the product of age times LDL (mg-years). The minimum threshold for a myocardial infarction (MI) in someone with a plasma LDL of 125 at age 40 is 5,000 mg-years. The goal of primary prevention is to delay reaching the minimal clinical threshold as long as possible. This review makes the case for a long-acting, lipid-lowering drug, administered annually starting at age 30, that could delay the threshold for MI until age 100.
冠状动脉疾病(CAD)的早期一级预防因缺乏生物标志物来检测年轻无症状个体的CAD风险而受到限制。尽管早期预防比二级干预更有效,但诸如高血压等传统风险因素通常要到生命的第五或第六个十年才会出现。相反,占所有CAD风险50%的遗传风险在受孕时随机分布且不随年龄变化;因此,出生后任何时候都可以使用遗传多基因风险评分(PRS)来确定。遗传风险会因生活方式的改变而显著改变,特别是降低低密度脂蛋白(LDL)水平。CAD风险取决于血浆LDL的浓度和暴露持续时间,这通过年龄乘以LDL(mg-年)的乘积来估计。40岁时血浆LDL为125的人发生心肌梗死(MI)的最低阈值是5000mg-年。一级预防的目标是尽可能长时间地推迟达到最低临床阈值。这篇综述支持一种长效降脂药物,从30岁开始每年给药一次,它可以将MI阈值推迟到100岁。