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前蛋白转化酶枯草溶菌素9(PCSK9)单克隆抗体在肌酸磷酸激酶水平显著升高患者中的安全性及临床疗效分析

A safety and clinical efficacy analysis of PCSK9 monoclonal antibodies in patients with markedly elevated creatine phosphokinase levels.

作者信息

Volis Ina, Hislop Eric, Saliba Walid, Zafrir Barak

机构信息

Department of Internal Medicine, Rambam Medical Center Haifa, Israel.

Faculty of Medicine, Technion, Israel Institute of Medicine Haifa, Israel.

出版信息

Am J Blood Res. 2021 Aug 15;11(4):399-404. eCollection 2021.

Abstract

INTRODUCTION

PCSK9 inhibitors (PCSK9i) are often used in statin-intolerant patients, aiming to reduce low-density lipoprotein cholesterol (LDL-C). Along with the growing experience with their use, there is a lack of evidence regarding the safety, tolerability, and clinical utility of PCSK9i in patients with markedly elevated creatine phosphokinase (CPK) levels.

METHODS

We screened a comprehensive HMO database for patients treated with PCSK9i (Jan 2016-Dec 2019), in whom elevated CPK levels (>1,000 U/L) were documented prior to the initiation of therapy. Treatment plans, adherence, and the levels of CPK and LDL-C were analyzed.

RESULTS

Of the 1,600 patients initiating treatment with PCSK9i, 26 had prior CPK values >1,000 U/L [median (IQR): 3,687 (1,876-8,344) U/L]. All 26 patients were previously treated with statins, which presumably resulted in adverse effects (myalgia in 24, and rhabdomyolysis in 5 patients) therefore mandating their discontinuation. Concomitant secondary factors for CPK elevation were present in 11 patients, and included renal failure, rheumatoid disorders, hypothyroidism, intensive exercise, proteinuria and genetic muscular disease. Of the 26 patients treated with PCSK9i, alirocumab was administered to 12 patients, and evolocumab to 14. Following the initiation of treatment with either drug, 24 patients (92%) demonstrated a reduction in CPK of >50%, and in 12 (46%) CPK levels have returned to normal values. With regard to treatment goals, 17 patients (65%) have achieved an LDL-C level of <70 mg/dL, and 12 (46%) have reached a level of <55 mg/dL. No serious adverse reactions were documented, and only 2 patients discontinued the treatment (not due to muscle symptoms or CPK elevation).

CONCLUSIONS

PCSK9i constitute a safe, tolerable, and effective treatment for hyperlipidemia in patients with markedly elevated CPK. While statin intolerance is a major cause for CPK elevation, concomitant etiologies for increased CPK values were rather common.

摘要

引言

前蛋白转化酶枯草溶菌素9抑制剂(PCSK9i)常用于他汀类药物不耐受的患者,旨在降低低密度脂蛋白胆固醇(LDL-C)。随着其使用经验的不断积累,关于PCSK9i在肌酸磷酸激酶(CPK)水平显著升高的患者中的安全性、耐受性及临床应用价值,仍缺乏证据。

方法

我们在一个综合的健康维护组织(HMO)数据库中筛选了2016年1月至20l9年12月接受PCSK9i治疗的患者,这些患者在开始治疗前记录有CPK水平升高(>1000 U/L)。分析了治疗方案、依从性以及CPK和LDL-C水平。

结果

在1600例开始接受PCSK9i治疗的患者中,26例之前的CPK值>1000 U/L[中位数(四分位间距):3687(1876 - 8344)U/L]。所有26例患者之前均接受过他汀类药物治疗,可能因此出现了不良反应(24例有肌痛,5例有横纹肌溶解),所以不得不停药。11例患者存在导致CPK升高的伴随次要因素,包括肾衰竭、类风湿性疾病、甲状腺功能减退、剧烈运动、蛋白尿和遗传性肌肉疾病。在接受PCSK9i治疗的26例患者中,12例使用了阿利西尤单抗,14例使用了依洛尤单抗。开始使用这两种药物中的任何一种治疗后,24例患者(92%)的CPK降低>50%,12例(46%)的CPK水平恢复到正常。关于治疗目标,17例患者(65%)的LDL-C水平降至<70 mg/dL,12例(46%)降至<55 mg/dL。未记录到严重不良反应,只有2例患者停药(并非由于肌肉症状或CPK升高)。

结论

对于CPK水平显著升高的患者,PCSK9i是一种安全、耐受性良好且有效的高脂血症治疗方法。虽然他汀类药物不耐受是CPK升高的主要原因,但导致CPK值升高的伴随病因相当常见。

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本文引用的文献

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Safety and Tolerability of PCSK9 Inhibitors: Current Insights.PCSK9抑制剂的安全性与耐受性:当前见解
Clin Pharmacol. 2020 Dec 11;12:191-202. doi: 10.2147/CPAA.S288831. eCollection 2020.
3
Successful treatment of a patient with mitochondrial myopathy with alirocumab.成功用阿利西尤单抗治疗 1 例线粒体肌病患者。
J Clin Lipidol. 2020 Sep-Oct;14(5):646-648. doi: 10.1016/j.jacl.2020.07.007. Epub 2020 Jul 24.
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Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome.依洛尤单抗与急性冠脉综合征后的心血管结局。
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