Literature DB >> 3924065

A comparative study of the effects of acipimox and clofibrate in type III and type IV hyperlipoproteinemia.

P M Stuyt, A F Stalenhoef, P N Demacker, A Van 't Laar.   

Abstract

Acipimox, an analogue of nicotinic acid, is a hypolipidemic drug with antilipolytic activity. Ten patients with type III and 10 with type IV hyperlipoproteinemia participated in a comparative open cross-over study of the effect of acipimox (750 mg/day) and clofibrate (2 g/day) on lipoproteins, apoliproproteins and postheparin lipase activities during 6 weeks. During acipimox treatment 2 type III patients complained of flushing, resulting in one drop-out. In the type III patients serum cholesterol decreased 30% (P less than 0.01) during treatment with acipimox and 24% (P less than 0.01) with clofibrate, and serum triglycerides 48% (P less than 0.01) and 34% (P less than 0.01), respectively. In the type IV patients serum cholesterol remained unchanged and serum triglycerides decreased 34% (P less than 0.05) and 35% (P less than 0.01), respectively. HDL cholesterol increased during treatment with both drugs in both groups between 6 and 15% (P less than 0.05) mainly due to a rise in HDL3 cholesterol (d greater than 1.100 g/ml). LDL cholesterol increased significantly during treatment with clofibrate, but not with acipimox. There were no or slight changes in the apoproteins A and B. Postheparin lipoprotein lipase increased during clofibrate treatment and hepatic lipase decreased during acipimox treatment. We concluded that acipimox in a dose of 750 mg/day has a similar hypolipidemic effect as 2 g clofibrate daily in type III and IV hyperlipoproteinemia.

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Year:  1985        PMID: 3924065     DOI: 10.1016/0021-9150(85)90165-0

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  7 in total

1.  A comparison of acipimox and nicotinic acid in type 2b hyperlipidaemia.

Authors:  M J O'Kane; T R Trinick; M B Tynan; E R Trimble; D P Nicholls
Journal:  Br J Clin Pharmacol       Date:  1992-04       Impact factor: 4.335

2.  Mechanism of anti-lipolytic action of acipimox in isolated rat adipocytes.

Authors:  A W Christie; D K McCormick; N Emmison; F B Kraemer; K G Alberti; S J Yeaman
Journal:  Diabetologia       Date:  1996-01       Impact factor: 10.122

3.  Increased affinity of LDL for their receptors after acipimox treatment in hypertriglyceridemia.

Authors:  G Franceschini; F Bernini; S Michelagnoli; S Bellosta; V Vaccarino; C Torre; F Pazzucconi; R Fumagalli; C R Sirtori
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

4.  Acipimox stimulates skin blood flow by a cyclo-oxygenase-dependent mechanism.

Authors:  A Edlund; L Musatti; A Wennmalm
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

5.  Effects of acipimox on haemorheology and plasma lipoproteins in patients with mixed hyperlipoproteinaemia.

Authors:  C Otto; K G Parhofer; M M Ritter; W O Richter; P Schwandt
Journal:  Br J Clin Pharmacol       Date:  1998-11       Impact factor: 4.335

6.  Acipimox-induced facial skin flush: frequency, thermographic evaluation and relationship to plasma acipimox level.

Authors:  A E Pontiroli; B Fattor; G Pozza; E Pianezzola; M Strolin Benedetti; L Musatti
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

7.  Effects of acipimox and cholestyramine on serum lipoproteins, non-cholesterol sterols and cholesterol absorption and elimination.

Authors:  H Gylling; H Vanhanen; T A Miettinen
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

  7 in total

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