Almutairi Abdulaali R, Alshahrani Walaa A, Alhathlol Ghaida K, Alsheikh Fatimah, Alakeel Abdulaziz, Al Yami Majed S, Fouda Mohammad, Almohammed Omar A, Alhamed Meshal S, Hafiz Awatif, Kutbi Hussam, Bagalagel Alaa, Alharbi Aisha, Alaboud Mashael, Aljohani Sarah, Ashram Waddah
Drug Sector, Saudi Food and Drug Authority, Riyadh, Saudi Arabia.
Department of Pharmacy Practice, College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Pharmacy Practice, Riyadh, Saudi Arabia.
Saudi Pharm J. 2024 Dec;32(12):102203. doi: 10.1016/j.jsps.2024.102203. Epub 2024 Nov 4.
Evolocumab's short-term efficacy and safety were proven in phase-3 clinical trial, but its long-term safety and effectiveness in the Saudi population are yet to be studied. The aim of this study was to assess the long-term safety and effectiveness of evolocumab in Saudi patients with primary hypercholesterolemia or mixed dyslipidemia.
A retrospective cohort study evaluated adult patients who had newly been prescribed evolocumab for hypercholesterolemia or mixed dyslipidemia. Safety events included myocardial infarction, unstable angina, stroke, transient ischemic attack, heart failure, rhabdomyolysis, renal dysfunction, and myalgia. Effectiveness outcomes included changes in lipid profiles from baseline, assessed at 6-, 12-, 18-, and 24-month.
The study sample were 469 who newly prescribed evolocumab, from which 69.1 % being male, were included. The most prevalent comorbidities were coronary artery disease, diabetes, and hypertension. Statin was the most commonly used therapy. The most common adverse events at 6-month follow-up, based on the incidence rate per 1000 person-years, were coronary revascularization (63.20), myalgia (44.96), myocardial infarction (31.53), unstable angina (31.49), heart failure (26.94), rhabdomyolysis without renal dysfunction (8.93), transient ischemic attack (4.46), and rhabdomyolysis with renal dysfunction (4.46). Stroke incidence increased with follow-up length, from 8.87 per 1000 person-years at 6 months to 12.84 per 1000 person-years at 24 months. Evolocumab use significantly reduced LDL and total cholesterol levels at 6, 12, 18, and 24 months follow-up, while having no significant effect on HDL or triglycerides levels.
Evolocumab appeared to be safe and effective therapeutic option for patients with primary hypercholesterolemia or mixed dyslipidemia to potentially reduce LDL levels to therapeutic levels when statins are insufficient.
依洛尤单抗的短期疗效和安全性已在3期临床试验中得到证实,但其在沙特人群中的长期安全性和有效性尚未得到研究。本研究的目的是评估依洛尤单抗在沙特原发性高胆固醇血症或混合性血脂异常患者中的长期安全性和有效性。
一项回顾性队列研究评估了新开具依洛尤单抗治疗高胆固醇血症或混合性血脂异常的成年患者。安全事件包括心肌梗死、不稳定型心绞痛、中风、短暂性脑缺血发作、心力衰竭、横纹肌溶解、肾功能不全和肌痛。有效性结果包括在6、12、18和24个月时评估的血脂谱相对于基线的变化。
该研究样本包括469名新开具依洛尤单抗的患者,其中69.1%为男性。最常见的合并症是冠状动脉疾病、糖尿病和高血压。他汀类药物是最常用的治疗方法。在6个月随访时,基于每1000人年发病率计算,最常见的不良事件是冠状动脉血运重建(63.20)、肌痛(44.96)、心肌梗死(31.53)、不稳定型心绞痛(31.49)、心力衰竭(26.94)、无肾功能不全的横纹肌溶解(8.93)、短暂性脑缺血发作(4.46)和伴有肾功能不全的横纹肌溶解(4.46)。中风发病率随随访时间延长而增加,从6个月时的每1000人年8.87例增加到24个月时的每1000人年12.84例。在6、12、18和24个月随访时,使用依洛尤单抗可显著降低低密度脂蛋白和总胆固醇水平,而对高密度脂蛋白或甘油三酯水平无显著影响。
对于原发性高胆固醇血症或混合性血脂异常患者,当他汀类药物治疗不足时,依洛尤单抗似乎是一种安全有效的治疗选择,有可能将低密度脂蛋白水平降低到治疗水平。