Literature DB >> 1648647

[Lipid status and basal steroid hormone level following 16 weeks of lovastatin therapy in primary hypercholesterolemia].

W Stürmer1, E P Kromer, A J Riegger, K Kochsiek.   

Abstract

We examined the effect of a 16 week therapy with the HMG CoA reductase inhibitor lovastatin in 29 patients (mean age 43 years) with primary hypercholesterolemia. All patients had cholesterol levels above 250 mg/dl (mean 348 +/- 96 mg/dl) inspite of a lipid lowering diet and a therapy with conventional lipid lowering drugs during a three month screening period. After 4 weeks on placebo 20 mg lovastatin was given orally for 4 weeks. If total cholesterol exceeded 200 mg/dl the dose of lovastatin was increased monthly by 20 mg up to the maximal dose of 80 mg/day. After 16 weeks lipid values changed compared with the placebo period: total-cholesterol -25%, triglycerides -8.6%, LDL-cholesterol -31%, APO B -25%, HDL-cholesterol +5.8%, APO AI +0.8%, total-cholesterol/HDL-cholesterol -25%. There was a significant improvement of lipid parameters after lovastatin therapy compared with conventional lipid lowering drugs at the end of the screening period. Lovastatin was well tolerated. A small and reversible rise of transaminases and/or creatinine kinase was observed in 6 patients. Basal levels of ACTH in the morning increased significantly during lovastatin therapy within the normal range. This observation was more frequent in females (10/12) than in males (10/17).

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Year:  1991        PMID: 1648647     DOI: 10.1007/bf01644764

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  25 in total

1.  [Lowering of the plasma lipid concentration with lovastatin. A clinical study in patients with primary hypercholesterolemia].

Authors:  S Grüneberger; M Dreyer; R Kangah; A Reinicke; C Staisch; E Steinhagen-Thiessen; P Müller; B Simon; H G Dammann
Journal:  Dtsch Med Wochenschr       Date:  1989-11-10       Impact factor: 0.628

Review 2.  Lipoprotein receptors in the liver. Control signals for plasma cholesterol traffic.

Authors:  M S Brown; J L Goldstein
Journal:  J Clin Invest       Date:  1983-09       Impact factor: 14.808

3.  New developments in lipid-lowering therapy: the role of inhibitors of hydroxymethylglutaryl-coenzyme A reductase.

Authors:  J A Tobert
Journal:  Circulation       Date:  1987-09       Impact factor: 29.690

4.  Testicular function in type II hyperlipoproteinemic patients treated with lovastatin (mevinolin) or neomycin.

Authors:  W H Farnsworth; J M Hoeg; M Maher; E H Brittain; R J Sherins; H B Brewer
Journal:  J Clin Endocrinol Metab       Date:  1987-09       Impact factor: 5.958

Review 5.  3-Hydroxy-3-methylglutaryl--coenzyme A reductase inhibitors in the treatment of hypercholesterolemia.

Authors:  J M Hoeg; H B Brewer
Journal:  JAMA       Date:  1987-12-25       Impact factor: 56.272

Review 6.  Discovery, biochemistry and biology of lovastatin.

Authors:  A W Alberts
Journal:  Am J Cardiol       Date:  1988-11-11       Impact factor: 2.778

7.  Regulation of low-density lipoprotein receptors: implications for pathogenesis and therapy of hypercholesterolemia and atherosclerosis.

Authors:  J L Goldstein; M S Brown
Journal:  Circulation       Date:  1987-09       Impact factor: 29.690

Review 8.  Bezafibrate. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hyperlipidaemia.

Authors:  J P Monk; P A Todd
Journal:  Drugs       Date:  1987-06       Impact factor: 9.546

9.  Mevinolin plus colestipol in therapy for severe heterozygous familial hypercholesterolemia.

Authors:  D R Illingworth
Journal:  Ann Intern Med       Date:  1984-11       Impact factor: 25.391

10.  The influence of mevinolin on the adrenal cortical response to corticotropin in heterozygous familial hypercholesterolemia.

Authors:  D R Illingworth; D Corbin
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205

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