J Lipid Atheroscler.  2023 Sep;12(3):277-289. 10.12997/jla.2023.12.3.277.

Lipid-Lowering Efficacy of Combination Therapy With ModerateIntensity Statin and Ezetimibe Versus High-Intensity Statin Monotherapy: A Randomized, Open-Label, NonInferiority Trial From Korea

Affiliations
  • 1Cardiovascular Center, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea
  • 2Department of Cardiology, Korea University Ansan Hsopital, Ansan, Korea
  • 3Division of Cardiology, Department of Internal Medicine, NHIS Ilsan Hospital, Goyang, Korea
  • 4Department of Cardiology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam, Korea
  • 5Cardiovascular Center Kangdong Sacred Heart Hospital Hallym University, Seoul, Korea
  • 6Department of Internal Medicine, Bundang Jaesang General Hospital, Seongnam, Korea

Abstract


Objective
This phase IV, multicenter, randomized controlled, open-label, and parallel clinical trial aimed to compare the efficacy and safety of ezetimibe and moderate intensity rosuvastatin combination therapy to that of high intensity rosuvastatin monotherapy in patients with atherosclerotic cardiovascular disease (ASCVD).
Methods
This study enrolled patients with ASCVD and after a four-week screening period, patients were randomly assigned to receive either rosuvastatin and ezetimibe (RE 10/10 group) or high-intensity rosuvastatin (R20 group) only in a 1:1 ratio. The primary outcome was the difference in the percent change in the mean low-density lipoprotein cholesterol (LDL-C) level from baseline to 12 weeks between two groups after treatment.
Results
The study found that after 12 and 24 weeks of treatment, the RE10/10 group had a greater reduction in LDL-C level compared to the R20 group (−22.9±2.6% vs. −15.6 ± 2.5% [p=0.041] and −24.2±2.5% vs. −12.9±2.4% [p=0.001] at 12 and 24 weeks, respectively). Moreover, a greater number of patients achieved the target LDL-C level of ≤70 mg/dL after the treatment period in the combination group (74.6% vs. 59.9% [p=0.012] and 76.2% vs. 50.8% [p<0.001] at 12 and 24 weeks, respectively). Importantly, there were no significant differences in the occurrence of overall adverse events and adverse drug reactions between two groups.
Conclusion
Moderate-intensity rosuvastatin and ezetimibe combination therapy had better efficacy in lowering LDL-C levels without increasing adverse effects in patients with ASCVD than high-intensity rosuvastatin monotherapy.

Keyword

Rosuvastatin calcium; Ezetimibe; Cholesterol, LDL; Cardiovascular diseases
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