Ewha Med J.  2001 Sep;24(3):103-108. 10.12771/emj.2001.24.3.103.

Clinical Efficacy and Safety of Cerivastatin(LIPOBAY(R)) in Patients with Hypercholesterolemia

Affiliations
  • 1Department of Internal Medicine, Medical Research Center, College of Medicine, Ewha Womans University, Korea.
  • 2Department of Internal Medicine, Seoul Red Cross Hospital, Korea.

Abstract


OBJECTIVES
Cerivastain(LIPOBAY(R)) is recently developed HMG-CoA reductase inhibitor which is effective in lowering serum cholesterol levels at microgram does. We evaluated the clinical efficacy and safety of cerivastatin(LIPOBAY(R)) in patients with hypercholesterolemia. METHOD: Thirty-seven patients(male : 13, female : 24) with hypercholesteolemia defined as baseline serum total cholesterol > or =240mg/dl, or > or =220mg/dl in patients with known coronary artery disease were included for this study. After 2 weeks of low cholesterol diet, if the serum total choesterol level meet the criteria, cerivastain 0.4mg/day was prescribed for 8 weeks. Clinical follow-up and laboratory tests were performed 4 weeks and 8 weeks after medication.
RESULTS
After 4 weeks of cerivastain 0.4mg/day treatment, low density lipoprotein(LDL) cholesterol decreased 38% and total cholesterol decreased 28.8% from baseline. Triglyceride decreased 11.6%, and high density lipoprotein(HDL) cholesterol decreased 7.8% from baseline. Total cholesterol/HDL ratio decreased 20.8% and LDL/HDL ratio decreased 31.1% from baseline. After 8 weeks of treatment, no further significant changes were noted compared with the values at 4 weeks. Cervastatin was discontinued in one patient(2.7%) due to continuous liver enzyme elevation.
CONCLUSION
Cerivastatin 0.4mg/day is effective in lowering serum cholesterol levels without significant adverse reactions. Cerivastatin is effective and safe for patients with hypercholesterolemia who needs aggressive LDL cholesterol lowering.

Keyword

Cerivastatin; Hypercholesterolemia

MeSH Terms

Cholesterol
Cholesterol, LDL
Coronary Artery Disease
Diet
Female
Follow-Up Studies
Humans
Hypercholesterolemia*
Liver
Oxidoreductases
Triglycerides
Cholesterol
Cholesterol, LDL
Oxidoreductases
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