Revankar Shruti, Park Jong Kun, Satish Priyanka, Agarwala Anandita
Department of Internal Medicine, Baylor College of Medicine, Houston, TX, USA.
Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Am J Prev Cardiol. 2024 Feb 15;17:100639. doi: 10.1016/j.ajpc.2024.100639. eCollection 2024 Mar.
As the global population ages and cardiovascular risk factors rise, we can expect a continued increase in atherosclerotic disease. Low-density lipoprotein cholesterol (LDL-C) reduction is a cornerstone of cardiovascular risk reduction with strong, causal evidence indicating that the greatest benefit is derived from early and large decreases in LDL-C. Despite the adoption of statins as the backbone of lipid-therapy regimens, numerous studies and registry analyses reveal our collective inability to achieve LDL-C goals in high-risk patients. Combination therapy with ezetimibe has been shown to result in statistically significant decreases in LDL-C level, atheroma volume, and cardiovascular adverse event rates. A major barrier to implementing an upfront combination therapy approach is the perceived side effects from therapeutic agents although multiple studies show that a therapeutic patient-physician relationship could overcome this issue. Novel agents such as PCSK-9 inhibitors, bempedoic acid, and inclisiran have the potential to achieve similar outcomes although additional research is needed regarding the cost effectiveness of these approaches. Despite these hurdles, there is a role for the newer agents early in the disease course of high-risk patients such as those with markedly elevated LDL-C >190 mg/dL and FH. The implementation of upfront combination therapy, especially in high-risk patients, will decrease clinical inertia while allowing for earlier consideration of newer, effective agents to decrease cardiovascular burden.
随着全球人口老龄化以及心血管危险因素增加,我们预计动脉粥样硬化疾病会持续增多。降低低密度脂蛋白胆固醇(LDL-C)是降低心血管风险的基石,有力的因果证据表明,最大益处源于早期大幅降低LDL-C。尽管他汀类药物已成为脂质治疗方案的基础,但众多研究和登记分析显示,我们总体上无法使高危患者达到LDL-C目标。已证明依折麦布联合治疗可使LDL-C水平、动脉粥样硬化斑块体积和心血管不良事件发生率在统计学上显著降低。实施早期联合治疗方法的一个主要障碍是人们认为治疗药物有副作用,尽管多项研究表明,良好的医患治疗关系可以克服这个问题。新型药物如前蛋白转化酶枯草溶菌素9(PCSK-9)抑制剂、贝派地酸和英克西兰有可能取得类似效果,不过这些方法的成本效益还需要更多研究。尽管有这些障碍,但对于高危患者,如LDL-C显著升高>190mg/dL和患有家族性高胆固醇血症(FH)的患者,在疾病早期使用这些新型药物仍有作用。实施早期联合治疗,尤其是在高危患者中,将减少临床惰性,同时允许更早考虑使用更新的有效药物来减轻心血管负担。