Chemical structure of lovastatin
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Lovastatin

Lovastatin is a member of the drug class of statins, used for lowering cholesterol and preventing cardiovascular disease (hypolipidemic agents). The mode of action of statins is HMG-CoA reductase enzyme inhibition. more...

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Lovastatin was isolated from a strain of Aspergillus terreus and it was the first statin approved by the FDA (August 1987).

Lovastatin is also naturally produced by certain higher fungii such as Pleurotus ostreatus (oyster mushroom) and closely related Pleurotus spp. (Bobek et al., 1998)

In 1998, the US FDA placed a ban on the sale of dietary supplements derived from red yeast rice, which naturally contains lovastatin, arguing that products containing prescription agents require drug approval.

Brand names

  • Mevacor®
  • Advicor® (as a combination with niacin)
  • Altocor®
  • Altoprev®

Reference

  • Bobek P, Ozdin L, Galbavy S. Dose- and time-dependent hypocholesterolemic effect of oyster mushroom (Pleurotus ostreatus) in rats. Nutrition 1998;14:282-6. PMID 9583372.


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Use of lovastatin in blacks with hypercholesterolemia - Tips from Other Journals
From American Family Physician, 1/15/98 by Grace Brooke Huffman

Black patients have almost twice the age-adjusted risk of dying from coronary heart disease as do white patients. Lipid-lowering drugs are known to have a beneficial effect on risk factors such as hypercholesterolemia. However, few studies have evaluated the efficacy of the use of lipid-lowering drugs in this population. Fong and Ward conducted a double-blind controlled trial to evaluate the efficacy of lovastatin in black patients with primary hypercholesterolemia.

Patients were included in the study if they had a diagnosis of hypercholesterolemia and met National Cholesterol Education Program (NCEP II) guidelines for the use of medication to treat elevated cholesterol levels. Patients with diabetes mellitus, hypothyroidism and liver or renal disease were excluded from the study. Recent myocardial infarction and coronary artery bypass surgery were also exclusion criteria. A total of 41 patients completed the study. Lipid profiles and other blood chemistries were performed for each patient. Patients were then randomized to receive either placebo or 20 mg of lovastatin daily. All of the patients were counseled about the American Heart Association Step One Diet for lowering serum cholesterol.

Total cholesterol was reduced by 14.7 percent in the lovastatin group, compared with no reduction in cholesterol in the placebo group. Low-density lipoprotein levels decreased by 20 percent in the treatment group, and triglyceride levels decreased 10.5 percent in the treatment group. Several patients in the treatment group reached their target low-density lipoprotein levels (as established by the NCEP II guidelines), but none of the placebo-treated group reached the NCEP II goal. Neither group experienced any serious side effects, although four patients in the treatment group discontinued their medication for various reasons, including gastrointestinal upset. Previous studies have shown that black patients are less likely than white patients to be treated for hypercholesterolemia (odds ratio: 0.81).

The authors conclude that lovastatin and probably other HMG-CoA reductase inhibitors are efficacious in the treatment of hypercholesterolemia, and should be used more frequently in the black population when indicated for the treatment of hypercholesterolernia.

Fong RL, Ward HJ. The efficacy of lovastatin in lowering cholesterol in African Americans with primary hypercholesterolemia. Am J Med 1997,-102:387-91.

COPYRIGHT 1998 American Academy of Family Physicians
COPYRIGHT 2000 Gale Group

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