Di Fusco Stefania Angela, Maggioni Aldo Pietro, Bernelli Chiara, Perone Francesco, De Marzo Vincenzo, Conte Edoardo, Musella Francesca, Uccello Giuseppe, Luca Leonardo De, Gabrielli Domenico, Gulizia Michele Massimo, Oliva Fabrizio, Colivicchi Furio
Emergency Department, Clinical and Rehabilitation Cardiology Unit, San Filippo Neri Hospital, ASL Roma 1, 00135 Rome, Italy.
ANMCO Research Center, Heart Care Foundation, 50121 Florence, Italy.
Rev Cardiovasc Med. 2022 Nov 3;23(11):375. doi: 10.31083/j.rcm2311375. eCollection 2022 Nov.
Therapeutic approaches based on gene silencing technologies represent a new opportunity to manage hypercholesterolemia. Inclisiran is a small interfering RNA that targets proprotein convertase subtilisin/kexin type 9 (PCSK9) mRNA. Clinical studies have demonstrated that inclisiran is effective, safe, and well-tolerated in reducing low-density lipoprotein cholesterol (LDL-C) in patients with familial hypercholesterolemia, atherosclerotic cardiovascular disease, and atherosclerotic cardiovascular disease risk equivalents. A meta-analysis of phase 3 trials demonstrated a 51% reduction in LDL-C levels at 18 months as compared with placebo. Adverse event incidence was found to be comparable in individuals treated with inclisiran and those receiving placebo, though the reactions at the site of injection were more common in patients receiving inclisiran as compared with those receiving placebo. The recommended inclisiran dose is 284 mg administered as a subcutaneous injection to be repeated after three months with a subsequent 6-month maintenance regimen. Overall, since the pharmacological efficacy of inclisiran in LDL-C reduction is comparable to that of monoclonal antibodies against PCSK9, the longer effect duration and the favorable safety profile may favor this newer approach for hypercholesterolemia management.
基于基因沉默技术的治疗方法为高胆固醇血症的治疗带来了新机遇。英克西兰是一种靶向前蛋白转化酶枯草溶菌素9型(PCSK9)信使核糖核酸(mRNA)的小干扰RNA。临床研究表明,英克西兰在降低家族性高胆固醇血症、动脉粥样硬化性心血管疾病及动脉粥样硬化性心血管疾病风险等同症患者的低密度脂蛋白胆固醇(LDL-C)方面有效、安全且耐受性良好。一项对3期试验的荟萃分析表明,与安慰剂相比,18个月时英克西兰治疗组的LDL-C水平降低了51%。虽然与接受安慰剂的患者相比,接受英克西兰治疗的患者注射部位反应更常见,但发现英克西兰治疗组和接受安慰剂组的不良事件发生率相当。英克西兰的推荐剂量为284毫克,皮下注射,三个月后重复给药,随后进行6个月的维持治疗方案。总体而言,由于英克西兰降低LDL-C的药理疗效与抗PCSK9单克隆抗体相当,其更长的作用持续时间和良好的安全性可能使这种新方法更有利于高胆固醇血症的治疗。