Literature DB >> 7517834

Gender-related response to fluvastatin in patients with heterozygous familial hypercholesterolaemia.

E Leitersdorf1.   

Abstract

Hydroxymethylglutaryl coenzyme A (HMG CoA) reductase inhibitors are potent cholesterol reducing agents that have been successfully used for the treatment of heterozygous familial hypercholesterolaemia (FH). A recent investigation revealed that several constitutional and genetic factors significantly determined the response of plasma lipids and lipoproteins to the HMG CoA reductase inhibitor fluvastatin. Gender has been identified through multivariate analysis as a major determinant of the plasma high density lipoprotein (HDL) cholesterol response. The current analysis was undertaken to determine possible gender-related fluvastatin dose-response differences. The analysis revealed that for HDL cholesterol, gender-related differences reach statistical significance only at the highest fluvastatin dose of 40 mg/day (females 22.9%, males 12.9%, p < 0.01). In parallel, the change in low density lipoprotein (LDL) cholesterol: HDL cholesterol ratio, an indicator of ischaemic heart disease risk, was also found to be affected by gender (females -38.4%, males -32.2%, p < 0.01). For LDL cholesterol, no consistent gender-related differences were found. In conclusion, the response of plasma lipid levels to fluvastatin in heterozygote FH patients is significantly affected by gender, with females achieving a more marked overall response, as indicated by higher HDL cholesterol levels and a lower LDL cholesterol: HDL cholesterol ratio.

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Year:  1994        PMID: 7517834     DOI: 10.2165/00003495-199400472-00010

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  11 in total

1.  Influence of age and gender on the plasma profiles of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitory activity following multiple doses of lovastatin and simvastatin.

Authors:  H Cheng; J D Rogers; A E Sweany; M R Dobrinska; E A Stein; A C Tate; R D Amin; H Quan
Journal:  Pharm Res       Date:  1992-12       Impact factor: 4.200

2.  A prospective study of obesity, lipids, apolipoproteins and ischaemic heart disease in women.

Authors:  M P Coleman; T J Key; D Y Wang; C Hermon; I S Fentiman; D S Allen; M Jarvis; M C Pike; T A Sanders
Journal:  Atherosclerosis       Date:  1992-02       Impact factor: 5.162

3.  Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge.

Authors:  W T Friedewald; R I Levy; D S Fredrickson
Journal:  Clin Chem       Date:  1972-06       Impact factor: 8.327

4.  Prognosis after initial myocardial infarction: the Framingham study.

Authors:  W B Kannel; P Sorlie; P M McNamara
Journal:  Am J Cardiol       Date:  1979-07       Impact factor: 2.778

5.  Efficacy and tolerability of lovastatin in 3390 women with moderate hypercholesterolemia.

Authors:  R H Bradford; M Downton; A N Chremos; A Langendörfer; S Stinnett; D T Nash; G Mantell; C L Shear
Journal:  Ann Intern Med       Date:  1993-06-01       Impact factor: 25.391

6.  A missense mutation in the low density lipoprotein receptor gene causes familial hypercholesterolemia in Sephardic Jews.

Authors:  E Leitersdorf; A Reshef; V Meiner; E J Dann; Y Beigel; F G van Roggen; D R van der Westhuyzen; G A Coetzee
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

7.  Genetic determinants of responsiveness to the HMG-CoA reductase inhibitor fluvastatin in patients with molecularly defined heterozygous familial hypercholesterolemia.

Authors:  E Leitersdorf; S Eisenberg; O Eliav; Y Friedlander; N Berkman; E J Dann; D Landsberger; E Sehayek; V Meiner; M Wurm
Journal:  Circulation       Date:  1993-04       Impact factor: 29.690

8.  Hypercholesterolemia in five Israeli Christian-Arab kindreds is caused by the "Lebanese" allele at the low density lipoprotein receptor gene locus and by an additional independent major factor.

Authors:  A Oppenheim; Y Friedlander; E J Dann; N Berkman; S P Schwartz; E Leitersdorf
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

9.  Haplotype analysis at the low density lipoprotein receptor locus: application to the study of familial hypercholesterolemia in Israel.

Authors:  N Berkman; B S Weir; S Pressman-Schwartz; A Reshef; E Leitersdorf
Journal:  Hum Genet       Date:  1992-02       Impact factor: 4.132

10.  Intensive combination drug therapy of familial hypercholesterolemia with lovastatin, probucol, and colestipol hydrochloride.

Authors:  J L Witztum; D Simmons; D Steinberg; W F Beltz; R Weinreb; S G Young; P Lester; N Kelly; J Juliano
Journal:  Circulation       Date:  1989-01       Impact factor: 29.690

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  3 in total

Review 1.  Fluvastatin: a review of its pharmacology and use in the management of hypercholesterolaemia.

Authors:  G L Plosker; A J Wagstaff
Journal:  Drugs       Date:  1996-03       Impact factor: 9.546

2.  A gene score of nine LDL and HDL regulating genes is associated with fluvastatin-induced cholesterol changes in women.

Authors:  Viktor Hamrefors; Marju Orho-Melander; Ronald M Krauss; Bo Hedblad; Peter Almgren; Göran Berglund; Olle Melander
Journal:  J Lipid Res       Date:  2009-09-22       Impact factor: 5.922

Review 3.  Fluvastatin for lowering lipids.

Authors:  Stephen P Adams; Sarpreet S Sekhon; Michael Tsang; James M Wright
Journal:  Cochrane Database Syst Rev       Date:  2018-03-06
  3 in total

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