Tziomalos Konstantinos
First Propedeutic Department of Internal Medicine, AHEPA Hospital, 1 Stilponos Kyriakidi street, Thessaloniki, 54636, Greece.
Curr Pharm Des. 2017;23(10):1495-1499. doi: 10.2174/1381612823666170201161631.
Treatment with statins substantially reduces cardiovascular morbidity and mortality both in patients with and without established cardiovascular disease. Accordingly, statins represent the cornerstone of lipid-lowering treatment. However, there are still unmet clinical needs in the management of dyslipidemia. Indeed, it is difficult to achieve low-density lipoprotein cholesterol (LDL-C) targets in many patients, particularly in those at very high cardiovascular risk or in those with very high baseline LDL-C levels [e.g. with heterozygous familial hypercholesterolemia (FH)]. Moreover, a sizable proportion of patients are not able to tolerate high doses of statins, mostly due to muscle-related adverse effects. In these patient populations, inhibition of proprotein convertase subtilisin-kexin type 9 (PCSK9) with monoclonal antibodies appears to represent a useful tool for achieving LDL-C targets.
In the present review, we summarize the current knowledge on the effects of the PCSK9 inhibitors alirocumab and evolocumab on lipid levels in various populations and discuss the role of these agents in the management of dyslipidemia.
In addition to a substantial reduction in LDL-C levels (by 50-60%), PCSK9 inhibitors also lower triglyceride, non-high-density lipoprotein cholesterol (non-HDL-C) and lipoprotein (a) levels and increase HDL-C levels. Preliminary data suggest that PCSK9 inhibitors are safe. However, ongoing randomized, placebo-controlled trials will provide definitive evidence on the safety of these novel agents and on their effects on cardiovascular morbidity and mortality.
Given the high cost of PCSK9 inhibitors, their use should be restricted to carefully selected, veryhigh risk patients until the results of these trials are available.
他汀类药物治疗可显著降低已患心血管疾病和未患心血管疾病患者的心血管发病率和死亡率。因此,他汀类药物是降脂治疗的基石。然而,在血脂异常的管理方面仍存在未满足的临床需求。事实上,许多患者难以实现低密度脂蛋白胆固醇(LDL-C)目标,特别是那些心血管风险极高或基线LDL-C水平非常高的患者[例如杂合子家族性高胆固醇血症(FH)患者]。此外,相当一部分患者无法耐受高剂量他汀类药物,主要是由于肌肉相关的不良反应。在这些患者群体中,使用单克隆抗体抑制前蛋白转化酶枯草溶菌素9型(PCSK9)似乎是实现LDL-C目标的有用工具。
在本综述中,我们总结了目前关于PCSK9抑制剂阿利西尤单抗和依洛尤单抗对不同人群血脂水平影响的知识,并讨论了这些药物在血脂异常管理中的作用。
除了使LDL-C水平大幅降低(降低50%-60%)外,PCSK9抑制剂还可降低甘油三酯、非高密度脂蛋白胆固醇(non-HDL-C)和脂蛋白(a)水平,并提高HDL-C水平。初步数据表明PCSK9抑制剂是安全的。然而,正在进行的随机、安慰剂对照试验将为这些新型药物的安全性及其对心血管发病率和死亡率的影响提供确凿证据。
鉴于PCSK9抑制剂成本高昂,在这些试验结果出来之前,其使用应仅限于经过精心挑选的极高风险患者。