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Published on: November 10, 2017
Systematic Review on Efficacy, Effectiveness, and Safety of Pitavastatin in Dyslipidemia in Asia
Nam Xuan Vo1, Huong Lai Pham1, Tan Trong Bui2
1Faculty of Pharmacy, Ton Duc Thang University, Ho Chi Minh City 700000, Vietnam.
Insights
Pitavastatin effectively lowers low-density lipoprotein cholesterol (LDL-C) in Asian populations, demonstrating comparable efficacy and safety to other statins for managing dyslipidemia.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Dyslipidemia is a major risk factor for cardiovascular disease (CVD).
- Statins are primary treatments for lowering low-density lipoprotein cholesterol (LDL-C).
- Pitavastatin (PIT) shows promise in lipid profile improvement.
Purpose of the Study:
- To systematically review the efficacy, effectiveness, and safety of pitavastatin in Asian dyslipidemia patients.
- To compare pitavastatin's lipid-lowering effects with other statins.
Main Methods:
- Systematic review of 17 studies (12 RCTs, 5 non-RCTs) from PubMed, Cochrane, Embase up to Nov 2024.
- Analysis focused on LDL-C reduction, safety, and adverse events, adhering to PRISMA guidelines.
- Study quality assessed using checklists to minimize bias.
Main Results:
- Pitavastatin (1-4 mg) achieved 28-47% LDL-C reduction, comparable to atorvastatin, rosuvastatin, and simvastatin.
- Pitavastatin 2 mg showed efficacy similar to atorvastatin 10 mg.
- High LDL-C target achievement rates (75-95%) with rare adverse events and low discontinuation rates.
Conclusions:
- Pitavastatin is a safe and effective alternative for dyslipidemia management in Asia.
- Further research is needed on long-term outcomes and high-risk populations.
Abstract:
Objectives: 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. Methods: 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. Results: 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. Conclusions: 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.
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