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Lovastatin wins cholesterol battle.


Lovastatin lovastatin /lo·va·stat·in/ (lo´vah-stat?in) an antihyperlipidemic agent that acts by inhibiting cholesterol synthesis, used in the treatment of hypercholesterolemia and other forms of dyslipidemia and to lower the risks associated with  wins cholesterol battle

In the first large clinical study comparing two of the major drugs used to treat high serum cholesterol, researchers have concluded that lovastatin, a new drug approved last September (SN: 9/12/87, p.166), works more effectively and causes fewer side effects Side effects

Effects of a proposed project on other parts of the firm.
 than the standard cholestyramine cholestyramine /cho·le·sty·ra·mine/ (ko?le-sti´rah-men) see cholestyramine resin, under resin.

cho·le·styr·a·mine
n.
 resin therapy. The drugs are among the six approved for use in lowering the level of low-density lipoprotein low-density lipoprotein
n. Abbr. LDL
A lipoprotein that contains relatively high amounts of cholesterol and is associated with an increased risk of atherosclerosis and coronary artery disease.
 (LDL LDL - ["LDL: A Logic-Based Data-Language", S. Tsur et al, Proc VLDB 1986, Kyoto Japan, Aug 1986, pp.33-41]. ) cholesterol in the bloodstream. High LDL levels are believed to contribute to heart disease in some people.

Involving 264 men and women from 12 clinical centers across the United States, the study was coordinated by Merck, Sharp & Dohme of West Point, Pa., which makes lovastatin. Researchers found the average LDL cholesterol level dropped by 32 percent when a 20-milligram dose of lovastatin was given twice a day for 12 weeks. Patients experienced a 42 percent average reduction in LDL cholesterol after taking a 40-milligram dose over the same period. For patients taking cholestyramine resin, researchers reported a 23 percent lower LDL level after 12 grams of cholestyramine resin therapy twice a day (the maximum recommended dosage) for the same 12 weeks. All groups saw 85 percent of the reduction within two weeks after the study began.

Writing in the July 15 JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION JAMA: The Journal of the American Medical Association is an international peer-reviewed general medical journal, published 48 times per year by the American Medical Association. JAMA is the most widely circulated medical journal in the world. , the researchers report that only one serious side effect -- regional muscle pain experienced by a 65-year-old woman in the 40-mg dosage group--was thought to be directly linked to lovastatin, and ended when the patient stopped taking the drug. Less serious effects, such as constipation, were more common in the cholestyramine resin therapy group.

Both drugs slightly increased patients' levels of high-density lipoprotein cholesterol high-density lipoprotein cholesterol See HDL-cholesterol.  -- the so called "good cholesterol" that appears to protect against heart disease.

"Our study clearly demonstrates that lovastatin is both considerably more effective and much better tolerated than cholestyramine resin therapy," the researchers state. They recommend further testing on one aspect of the study: Women seemed to respond to lovastatin better than men, although there were no gender differences in responses to cholestyramine resin therapy.
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Copyright 1988, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:Science News
Date:Jul 23, 1988
Words:345
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