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前蛋白转化酶枯草溶菌素9(PCSK9)单克隆抗体依洛尤单抗和阿利西尤单抗的治疗潜力及批判性分析

Therapeutic Potential and Critical Analysis of the PCSK9 Monoclonal Antibodies Evolocumab and Alirocumab.

作者信息

White C Michael

机构信息

University of Connecticut School of Pharmacy and UCONN and Hartford Hospital, Storrs, CT, USA

出版信息

Ann Pharmacother. 2015 Dec;49(12):1327-35. doi: 10.1177/1060028015608487. Epub 2015 Sep 30.

DOI:10.1177/1060028015608487
PMID:26424774
Abstract

OBJECTIVE

To review the mechanism of action for PCSK9 monoclonal antibodies and critically evaluate the therapeutic potential of evolocumab and alirocumab in the treatment of hypercholesterolemia.

DATA SOURCES

Ovid MEDLINE search from 1980 to August 2015 using the terms PCSK9, evolocumab, and alirocumab with forward and backward citation tracking.

STUDY SELECTION AND DATA EXTRACTION

English-language trials and studies assessing the mechanism, efficacy, or safety of PCSK9 monoclonal antibodies were included.

DATA SYNTHESIS

PCSK9 monoclonal antibodies have a potent ability to reduce low-density lipoprotein (LDL) by almost 50% in controlled trials: -47.49% (95% CI = -69.6% to -25.4%). They have an acceptable safety profile with no significant elevations in Creatine Kinase (CK) (odds ratio [OR] = 0.72; 95% CI = 0.54 to 0.96) or serious adverse events (OR = 1.01; 95% CI = 0.87 to 1.18), and preliminary evidence suggests reductions in myocardial infarction (OR = 0.49; 95% CI = 0.26 to 0.93). Although it is effective in several familial hypercholesterolemia (FH) patient types, it does not work in homozygous patients with dual allele LDL receptor negative polymorphisms or those who are homozygous for autosomal recessive hypercholesterolemia.

CONCLUSIONS

Although not preferred over statins because of limited clinical trial evidence of cardiovascular event reductions, dosing convenience, and expense, PCSK9 monoclonal antibodies will have a prominent role to play in the treatment of hypercholesterolemia, especially in patients needing large LDL reductions, including patients with many types of FH.

摘要

目的

回顾前蛋白转化酶枯草溶菌素9(PCSK9)单克隆抗体的作用机制,并严格评估依洛尤单抗和阿利西尤单抗在治疗高胆固醇血症方面的治疗潜力。

数据来源

使用PCSK9、依洛尤单抗和阿利西尤单抗等检索词,在1980年至2015年8月期间对Ovid MEDLINE进行检索,并进行前后引文跟踪。

研究选择与数据提取

纳入评估PCSK9单克隆抗体作用机制、疗效或安全性的英文试验和研究。

数据综合

在对照试验中,PCSK9单克隆抗体具有强大的降低低密度脂蛋白(LDL)的能力,可降低近50%:-47.49%(95%置信区间=-69.6%至-25.4%)。它们具有可接受的安全性,肌酸激酶(CK)无显著升高(优势比[OR]=0.72;95%置信区间=0.54至0.96)或严重不良事件(OR=1.01;95%置信区间=0.87至1.18),初步证据表明心肌梗死有所减少(OR=0.49;95%置信区间=0.26至0.93)。尽管它对几种家族性高胆固醇血症(FH)患者类型有效,但对双等位基因LDL受体阴性多态性的纯合患者或常染色体隐性高胆固醇血症纯合患者无效。

结论

尽管由于在降低心血管事件、给药便利性和费用方面的临床试验证据有限,PCSK9单克隆抗体不如他汀类药物受青睐,但它在高胆固醇血症治疗中将发挥重要作用,尤其是在需要大幅降低LDL的患者中,包括多种类型的FH患者。

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