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Plasma lipid lowering effects of doxazosin, a new selective alpha1 adrenergic inhibitor for systemic hypertension.

Abstract
Hypertension and hypercholesterolemia are 2 major risk factors for atherosclerotic coronary artery disease (CAD). Elevations of both blood pressure and serum cholesterol levels should be reduced to control CAD risk. Doxazosin is a once-daily, long-acting, selective alpha 1-adrenergic inhibitor that is effective for the treatment of essential hypertension. During controlled studies of doxazosin's antihypertensive efficacy, 3 serum lipid parameters were measured; total cholesterol, total triglyceride and high density lipoprotein (HDL) cholesterol. In 10- to 12-week placebo-controlled studies, 142 doxazosin-treated patients were compared with 155 placebo-controlled subjects. Doxazosin patients had an increase of 8.9% in the HDL/total cholesterol ratio (p less than 0.05), whereas total cholesterol, HDL cholesterol and triglyceride levels were not significantly different between the 2 study groups. During a 52-week comparison of doxazosin versus atenolol, doxazosin treatment was associated with a significant decrease in total triglyceride levels (5%; p less than 0.001) and increases in HDL cholesterol levels (3.9%; p less than 0.01) and HDL/total cholesterol ratio (5.4%; p less than 0.0001). Doxazosin is an effective antihypertensive agent that has a favorable impact on serum lipid levels, thereby promoting a beneficial effect on 2 major CAD risk factors.
AuthorsJ L Pool
JournalThe American journal of cardiology (Am J Cardiol) Vol. 59 Issue 14 Pg. 46G-50G (May 29 1987) ISSN: 0002-9149 [Print] United States
PMID2884853 (Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article)
Chemical References
  • Adrenergic alpha-Antagonists
  • Adrenergic beta-Antagonists
  • Antihypertensive Agents
  • Lipids
  • Placebos
  • Hydrochlorothiazide
  • Doxazosin
  • Prazosin
Topics
  • Adrenergic alpha-Antagonists (pharmacology)
  • Adrenergic beta-Antagonists (pharmacology)
  • Antihypertensive Agents (pharmacology)
  • Double-Blind Method
  • Doxazosin
  • Humans
  • Hydrochlorothiazide (pharmacology)
  • Hypertension (blood, drug therapy)
  • Lipids (blood)
  • Placebos
  • Prazosin (analogs & derivatives, pharmacology)

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