Saborowski Michael, Dölle Michael, Manns Michael P, Leitolf Holger, Zender Steffen
Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
Cardiol J. 2018;25(1):32-41. doi: 10.5603/CJ.a2017.0137. Epub 2017 Nov 23.
Proprotein convertase subtilisin/kexin type 9 (PCSK9)-inhibitors have shown great po-tential in efficient lipid lowering to achieve low-density lipoprotein-cholesterol (LDL-C) treatment goals. The aim of the study was too describe the clinical use of PCSK9-inhibitors and to investigate therapy adherence and safety outside of clinical trials.
Thirty-eight patients were treated with PSCK9-inhibitors. Patients were eligible for this therapy based on their individual cardiovascular risk and when all other available lipid-lowering regi-men had failed. Every patient answered a questionnaire concerning medical history and relevant side effects and therapy adherence.
Conventional therapy reduced patient LDL-C levels by about 38%. However, in 26 of the 38 patients, LDL-C treatment goals were not fulfilled because patients did not tolerate further dose es-calation due to side effects. Using a PCSK9 inhibitor, LDL-C levels were reduced by another 54% and 42% of patients reaching treatment goals. The results show that most patients still require concomitant therapy to reach LDL-C target levels. Three patients required dose reduction or change of the PCSK9 inhibitor. 16% did not inject the PCSK9 inhibitor regularly.
Only a minority of patients reached the recommended LDL-C goals. PCSK9-inhibitors were generally well tolerated. Despite low rates of reported side effects, therapy adherence was incom-plete, with 6 patients not injecting PCSK9-inhibitors on a regular basis. In-depth information about the medication and close supervision is advisable. PCSK9 inhibitors have shown great potential in aggressive lipid lowering therapy, but basic therapy is still required in most cases. Close supervision is recommended to improve therapy adherence. (Cardiol J 2018; 25, 1: 32-41).
前蛋白转化酶枯草溶菌素9型(PCSK9)抑制剂在有效降低血脂以实现低密度脂蛋白胆固醇(LDL-C)治疗目标方面显示出巨大潜力。本研究的目的是描述PCSK9抑制剂的临床应用,并调查临床试验之外的治疗依从性和安全性。
38例患者接受PCSK9抑制剂治疗。根据个体心血管风险以及所有其他可用降脂方案均失败的情况,患者符合该治疗条件。每位患者回答了一份关于病史、相关副作用和治疗依从性的问卷。
传统治疗使患者LDL-C水平降低约38%。然而,38例患者中有26例未达到LDL-C治疗目标,因为患者因副作用无法耐受进一步的剂量增加。使用PCSK9抑制剂后,LDL-C水平又降低了54%,42%的患者达到了治疗目标。结果表明,大多数患者仍需要联合治疗才能达到LDL-C目标水平。3例患者需要减少PCSK9抑制剂的剂量或更换药物。16%的患者未定期注射PCSK9抑制剂。
只有少数患者达到了推荐的LDL-C目标。PCSK9抑制剂总体耐受性良好。尽管报告的副作用发生率较低,但治疗依从性仍不完全,有6例患者未定期注射PCSK9抑制剂。建议提供关于药物的详细信息并进行密切监测。PCSK9抑制剂在积极的降脂治疗中显示出巨大潜力,但大多数情况下仍需要基础治疗。建议密切监测以提高治疗依从性。(《心脏病学杂志》2018年;25卷,第1期:32 - 41页)