Mhaimeed Omar, Burney Zain A, Schott Stacey L, Kohli Payal, Marvel Francoise A, Martin Seth S
Department of Medicine, Johns Hopkins Hospital, Baltimore, MD, United States.
Department of Medicine, Cleveland Clinic, Cleveland, OH, United States.
Am J Prev Cardiol. 2024 Mar 18;18:100649. doi: 10.1016/j.ajpc.2024.100649. eCollection 2024 Jun.
Cumulative exposure to low-density lipoprotein cholesterol (LDL-C) is a key driver of atherosclerotic cardiovascular disease (ASCVD) risk. An armamentarium of therapies to achieve robust and sustained reduction in LDL-C can reduce ASCVD risk. The gold standard for LDL-C assessment is ultracentrifugation but in routine clinical practice LDL-C is usually calculated and the most accurate calculation is the Martin/Hopkins equation. For primary prevention, consideration of estimated ASCVD risk frames decision making regarding use of statins and other therapies, and tools such as risk enhancing factors and coronary artery calcium enable tailoring of risk assessment and decision making. In patients with diabetes, lipid lowering therapy is recommended in most patients to reduce ASCVD risk with an opportunity to tailor therapy based on other risk factors. Patients with primary hypercholesterolemia and familial hypercholesterolemia (FH) with baseline LDL-C greater than or equal to 190 mg/dL are at elevated risk, and LDL-C lowering with high-intensity statin therapy is often combined with non-statin therapies to prevent ASCVD. Secondary prevention of ASCVD, including in patients with prior myocardial infarction or stroke, requires intensive lipid lowering therapy and lifestyle modification approaches. There is no established LDL-C level below which benefit ceases or safety concerns arise. When further LDL-C lowering is required beyond lifestyle modifications and statin therapy, additional medications include oral ezetimibe and bempedoic acid, or injectables such as PCSK9 monoclonal antibodies or siRNA therapy. A novel agent that acts independently of hepatic LDL receptors is evinacumab, which is approved for patients with homozygous FH. Other emerging agents are targeted at Lp(a) and CETP. In light of the expanding lipid treatment landscape, this manuscript reviews the importance of early, intensive, and sustained LDL-C-lowering for primary and secondary prevention of ASCVD.
低密度脂蛋白胆固醇(LDL-C)的累积暴露是动脉粥样硬化性心血管疾病(ASCVD)风险的关键驱动因素。一系列旨在实现LDL-C强劲且持续降低的治疗方法可降低ASCVD风险。LDL-C评估的金标准是超速离心法,但在常规临床实践中,LDL-C通常是计算得出的,最准确的计算方法是Martin/Hopkins方程。对于一级预防,考虑估计的ASCVD风险有助于决定是否使用他汀类药物和其他治疗方法,而诸如风险增强因素和冠状动脉钙化等工具可实现风险评估和决策的个性化。在糖尿病患者中,大多数患者建议进行降脂治疗以降低ASCVD风险,并可根据其他风险因素调整治疗方案。原发性高胆固醇血症和家族性高胆固醇血症(FH)且基线LDL-C大于或等于190 mg/dL的患者风险升高,高强度他汀类药物治疗降低LDL-C通常与非他汀类治疗联合使用以预防ASCVD。ASCVD的二级预防,包括既往有心肌梗死或中风的患者,需要强化降脂治疗和生活方式改变措施。目前尚无确定的LDL-C水平,低于该水平获益就会停止或出现安全问题。当生活方式改变和他汀类药物治疗之外还需要进一步降低LDL-C时,其他药物包括口服依折麦布和贝派地酸,或注射剂如PCSK9单克隆抗体或siRNA疗法。evinacumab是一种独立于肝脏LDL受体起作用的新型药物,已被批准用于纯合子FH患者。其他新兴药物针对脂蛋白(a)和胆固醇酯转运蛋白(CETP)。鉴于不断扩展的血脂治疗领域,本文综述了早期、强化和持续降低LDL-C对ASCVD一级和二级预防的重要性。