Vo Nam Xuan, Pham Huong Lai, Bui Tan Trong, Bui Tien Thuy
Faculty of Pharmacy, Ton Duc Thang University, Ho Chi Minh City 700000, Vietnam.
Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 700000, Vietnam.
Healthcare (Basel). 2024 Dec 31;13(1):59. doi: 10.3390/healthcare13010059.
Dyslipidemia, a significant risk factor for cardiovascular disease (CVD), is marked by abnormal lipid levels, such as the elevated lowering of low-density lipoprotein cholesterol (LDL-C). Statins are the first-line treatment for LDL-C reduction. Pitavastatin (PIT) has shown potential in lowering LDL-C and improving high-density lipoprotein cholesterol (HDL-C). This review assesses pitavastatin's efficacy, effectiveness, and safety in dyslipidemia management in Asia. A systematic review was conducted using PubMed, Cochrane, and Embase databases up to November 2024, adhering to Preferred Reporting Items of Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Seventeen studies (12 RCTs and 5 non-RCTs) were analyzed, focusing on LDL-C reduction, safety profiles, and adverse events. The quality of the studies was assessed using checklists to ensure the selection of the best studies and to limit bias. Pitavastatin doses (1-4 mg) reduced LDL-C by 28-47%, comparable to atorvastatin, rosuvastatin, and simvastatin. The 2 mg dose matched atorvastatin's 10 mg dose in efficacy for both short-term (35-42%) and long-term (28-36%) use. LDL-C target achievement rates were 75-95%. Adverse events, including mild myalgia and elevated liver enzymes, were rare, and discontinuation rates were low. Pitavastatin is an effective and safe alternative to traditional statins for dyslipidemia management in Asia. Further research on long-term outcomes and high-risk groups is warranted.
血脂异常是心血管疾病(CVD)的一个重要危险因素,其特征是血脂水平异常,如低密度脂蛋白胆固醇(LDL-C)升高或降低。他汀类药物是降低LDL-C的一线治疗药物。匹伐他汀(PIT)在降低LDL-C和提高高密度脂蛋白胆固醇(HDL-C)方面已显示出潜力。本综述评估了匹伐他汀在亚洲血脂异常管理中的疗效、有效性和安全性。使用PubMed、Cochrane和Embase数据库进行了一项系统综述,截至2024年11月,遵循系统评价和Meta分析的首选报告项目(PRISMA)指南。分析了17项研究(12项随机对照试验和5项非随机对照试验),重点关注LDL-C降低、安全性概况和不良事件。使用清单评估研究质量,以确保选择最佳研究并限制偏倚。匹伐他汀剂量(1-4毫克)可使LDL-C降低28-47%,与阿托伐他汀、瑞舒伐他汀和辛伐他汀相当。2毫克剂量在短期(35-42%)和长期(28-36%)使用时,在疗效上与阿托伐他汀的10毫克剂量相当。LDL-C目标达成率为75-95%。不良事件,包括轻度肌痛和肝酶升高,很少见,停药率也很低。在亚洲,匹伐他汀是血脂异常管理中传统他汀类药物的有效且安全的替代药物。有必要对长期结局和高危人群进行进一步研究。