Literature DB >> 3638181

Comparative efficacy of once versus twice daily mevinolin in the therapy of familial hypercholesterolemia.

D R Illingworth.   

Abstract

Mevinolin, a competitive inhibitor of the rate-limiting enzyme in cholesterol biosynthesis, is an effective hypocholesterolemic agent in patients with primary hypercholesterolemia when given in a twice-daily regimen. The present study compares the hypocholesterolemic effects of mevinolin given in a twice-daily dosage regimen with the same total dosage given either once in the morning or once in the evening in 12 patients with heterozygous familial hypercholesterolemia. Ten patients took a total daily dose of 40 mg of mevinolin and two took 20 mg. On the twice-daily dosage regimen, plasma concentrations of total cholesterol decreased 29.5% and 35.9% as compared with 21.4% and 26.9% with mevinolin given once in the morning and 27% and 32.2% with the drug given once in the evening. These values are all significantly different from baseline, but differences between the three treatment regimens do not reach statistical significance (P = 0.07 for the twice-daily versus once-in-the-morning dosage regimens). We conclude that once-daily administration of mevinolin, particularly in the evening, is an effective hypocholesterolemic regimen in patients with familial hypercholesterolemia.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3638181     DOI: 10.1038/clpt.1986.185

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  11 in total

1.  Clinical pharmacology of the hypocholesterolemic agent K 12.148 (lifibrol) in healthy volunteers.

Authors:  H Hasibeder; H J Staab; K Seibel; B Heibel; G Schmidle; W März
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

Review 2.  Clinical implications of new drugs for lowering plasma cholesterol concentrations.

Authors:  D R Illingworth
Journal:  Drugs       Date:  1991-02       Impact factor: 9.546

3.  Timing of intake of lipid lowering drugs: is that of importance?

Authors:  M Hanefeld
Journal:  Klin Wochenschr       Date:  1989-05-02

Review 4.  Lovastatin. A preliminary review of its pharmacodynamic properties and therapeutic use in hyperlipidaemia.

Authors:  J M Henwood; R C Heel
Journal:  Drugs       Date:  1988-10       Impact factor: 9.546

Review 5.  Chronotherapy versus conventional statins therapy for the treatment of hyperlipidaemia.

Authors:  Jose Manuel Izquierdo-Palomares; Jesus Maria Fernandez-Tabera; Maria N Plana; Almudena Añino Alba; Pablo Gómez Álvarez; Inmaculada Fernandez-Esteban; Luis Carlos Saiz; Pilar Martin-Carrillo; Óscar Pinar López
Journal:  Cochrane Database Syst Rev       Date:  2016-11-26

6.  Actual versus prescribed timing of lovastatin doses assessed by electronic compliance monitoring.

Authors:  W Kruse; T Nikolaus; J Rampmaier; E Weber; G Schlierf
Journal:  Eur J Clin Pharmacol       Date:  1993       Impact factor: 2.953

7.  Effects of pravastatin on plasma and urinary mevalonate concentrations in subjects with familial hypercholesterolaemia: a comparison of morning and evening administration.

Authors:  S Nozaki; T Nakagawa; A Nakata; S Yamashita; K Kameda-Takemura; T Nakamura; Y Keno; K Tokunaga; Y Matsuzawa
Journal:  Eur J Clin Pharmacol       Date:  1996       Impact factor: 2.953

8.  Pharmacodynamic effects and pharmacokinetics of a new HMG-CoA reductase inhibitor, rosuvastatin, after morning or evening administration in healthy volunteers.

Authors:  Paul D Martin; Patrick D Mitchell; Dennis W Schneck
Journal:  Br J Clin Pharmacol       Date:  2002-11       Impact factor: 4.335

9.  Time-dependent change in the effect of probucol in subjects with elevated cholesterol.

Authors:  A Fujimura; K Ohashi; A Ebihara
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

Review 10.  Drug-food interactions in hospitalised patients. Methods of prevention.

Authors:  I Gauthier; M Malone
Journal:  Drug Saf       Date:  1998-06       Impact factor: 5.606

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.