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Comparisons of three different doses of alirocumab application in patients with hypercholesterolemia: a meta-analysis
Yu-Sheng Zhang1, Ye-Hua Hao1, Hou-Long Luo2
1Department of Pharmacy, Guangdong Medical University, Guangdong, China.
Insights
The 75-150 mg dose of alirocumab every two weeks is most effective for lowering LDL cholesterol and increasing HDL cholesterol in hypercholesterolemia patients. This dosage is preferred over other alirocumab regimens for managing high cholesterol.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Clinical Trials
Background:
- Low high-density lipoprotein cholesterol (HDL-C) and high low-density lipoprotein cholesterol (LDL-C) are risk factors for cardiovascular disease (CVD).
- Alirocumab is a promising therapeutic agent for hypercholesterolemia.
- Optimizing alirocumab dosage is crucial for effective CVD risk management.
Purpose of the Study:
- To compare the efficacy of three different doses of alirocumab in patients with hypercholesterolemia.
- To determine the optimal alirocumab dosage regimen for lipid-lowering.
- To evaluate the impact of different alirocumab doses on lipid profiles and treatment goals.
Main Methods:
- A systematic review and meta-analysis of randomized controlled trials.
- Searched major databases including PubMed, EMBASE, PMC, and Cochrane Library.
- Subgroup analysis was used to compare different alirocumab doses (75-150 mg Q2W, 300 mg Q4W, 150 mg Q2W).
Main Results:
- Nine studies with 3870 patients were analyzed.
- Alirocumab 75-150 mg every two weeks (Q2W) significantly reduced LDL-C (MD, -55.17%) and increased HDL-C (MD, 7.70%) compared to other doses.
- No significant differences were observed in achieving LDL-C treatment goals (≤1.8 mmol/L), other lipid parameters, or adverse event incidence.
Conclusions:
- The alirocumab dosage of 75-150 mg Q2W is superior for improving LDL-C and HDL-C levels in hypercholesterolemia.
- This dosage regimen is recommended for patients requiring alirocumab therapy.
- Further research may explore long-term outcomes and specific patient subgroups.
Introduction:
Low high-density lipoprotein cholesterol (HDL-C) and high low-density lipoprotein cholesterol (LDL-C) levels are associated with incidence of cardiovascular disease (CVD). Alirocumab has been considered as an efficacious, safe and promising therapeutic modality for hypercholesterolemia. The purpose of this study is to compare the differences of the three different doses of alirocumab in patients with hypercholesterolemia.
Evidence Acquisition:
Randomized controlled trials were identified from PubMed, EMBASE, PMC and Cochrane-library databases. The inter-comparison of different doses were performed by subgroups analysis. Meta-analyses were performed by the Review Manager 5.3 and STATA 13.0 software.
Evidence Synthesis:
A total of nine studies involving 3870 patients were included in this meta-analysis. Alirocumab administered at 75-150 mg every 2 weeks (Q2W) resulted in a greater percent change from baseline in LDL-C concentrations (MD, -55.17; 95% CI: -64.35 to -45.99; P<0.05), and HDL-C levels (MD, 7.70; 95% CI 5.94 to 9.46; P<0.05) than other two doses (300 mg every 4 weeks [Q4W], 150 mg every 2 weeks [Q2W]). There was no difference in achieving the treatment goal of LDL-C (≤1.8 mmol/L), in other serum lipid parameters (total cholesterol [TC], triglyceride [TG]), and in the incidence of adverse events.
Conclusions:
The results demonstrate that alirocumab at a dose of 75-150 mg Q2W should be preferred in patients with hypercholesterolemia.
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