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Published on: November 10, 2017
Effect of lovastatin on serum lipids in patients with nonfamilial primary hypercholesterolemia
H D Itskovitz1, W Flamenbaum, C De Gaetano
1Department of Medicine, New York Medical College, Valhalla.
Insights
Lovastatin effectively lowers cholesterol in patients with primary hypercholesterolemia unresponsive to diet. This six-month study shows significant reductions in total cholesterol, LDL-C, and apo B-I with lovastatin treatment.
Area of Science:
- Cardiology
- Pharmacology
- Biochemistry
Background:
- Primary hypercholesterolemia (Types II-A and II-B) often requires pharmacologic intervention when diet alone is insufficient.
- Patients in this study were unresponsive to a six-week intensive dietary therapy program prior to lovastatin treatment.
Purpose of the Study:
- To evaluate the efficacy of lovastatin in reducing serum lipids.
- To assess the tolerability of lovastatin in patients with non-familial primary hypercholesterolemia.
Main Methods:
- An open-label study involving 38 patients with primary hypercholesterolemia.
- Lovastatin dosage started at 20 mg/day and titrated up to 80 mg/day, combined with ongoing dietary therapy.
- Serum lipid levels (TC, LDL-C, apo B-I, VLDL-C, triglycerides, HDL-C, apo A-I, apo A-II) were measured over a six-month period.
Main Results:
- Twenty-nine of 30 completers achieved significant reductions in total cholesterol (TC), LDL-C, and apo B-I.
- Lipid lowering effects were observed after one month and maintained throughout the six-month treatment.
- Comparative data showed TC decreased from 289 to 216 mg/dl, LDL-C from 206 to 141 mg/dl, and apo B-I from 112 to 89 mg/dl (all P < 0.0005).
- Slight, non-significant decreases in VLDL-C and triglycerides were noted, with insignificant increases in HDL-C, apo A-I, and apo A-II.
Conclusions:
- Lovastatin is effective in lowering serum lipids in patients with primary hypercholesterolemia who are unresponsive to dietary interventions.
- The drug demonstrated good tolerability and sustained lipid-lowering effects over six months.
- Lovastatin represents a viable therapeutic option for managing hypercholesterolemia when non-pharmacologic methods fail.
Abstract:
The effect of lovastatin on serum lipids and its tolerability in patients with non-familial primary hypercholesterolemia (type II-A and type II-B) during a six-month period were evaluated in this open-label study. Thirty-eight patients were enrolled in the study; tolerability was assessed in all 38 patients. Thirty patients completed the study, and the effect of lovastatin on serum lipids in these patients was assessed. Some patients had been treated for hypercholesterolemia with long-term dietary and other non-pharmacologic means before entry into the study. All patients were unresponsive to a six-week program of intensive dietary therapy and other nonpharmacologic treatment to lower their blood cholesterol levels before receiving lovastatin. While maintaining intensive dietary therapy, administration of lovastatin was instituted at a dosage of 20 mg/day, which was increased by 20-mg increments monthly, as necessary, to a maximum of 80 mg/day. In an effort to achieve goal levels of low-density lipoprotein cholesterol (LDL-C), ten patients received a daily dosage of 20 mg, 12 patients received 40 mg, seven patients 60 mg, and one patient 80 mg. Twenty-nine of the 30 patients achieved significant lowering of serum levels of total cholesterol (TC), LDL-C, and apolipoprotein (apo) B-I; this was demonstrated after the first month of therapy with lovastatin and was maintained throughout the six-month treatment period. One patient failed to demonstrate lowering of these serum lipids, despite receiving the maximum recommended dosage of lovastatin of 80 mg/day. Comparative measurements of serum lipids during dietary therapy alone and after six months of diet plus lovastatin therapy were as follows: TC, 289 +/- 5 versus 216 +/- 9 mg/dl (P less than 0.0005); LDL-C, 206 +/- 4 versus 141 +/- 5 mg/dl (P less than 0.0005); and apo B-I, 112 +/- 3 versus 89 +/- 2 mg/dl (P less than 0.0005). Serum levels of very-low-density lipoprotein cholesterol (VLDL-C) and triglycerides decreased slightly during lovastatin therapy, but the changes were not statistically significant. There were slight but statistically insignificant increases in serum levels of high-density lipoprotein cholesterol (HDL-C), apo A-I, and apo A-II.(ABSTRACT TRUNCATED AT 400 WORDS)
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