Literature DB >> 2390138

Influence of apo E polymorphism on the response to simvastatin treatment in patients with heterozygous familial hypercholesterolemia.

P De Knijff1, A F Stalenhoef, M J Mol, J A Gevers Leuven, J Smit, D W Erkelens, J Schouten, R R Frants, L M Havekes.   

Abstract

In a group of 120 patients with heterozygous familial hypercholesterolemia (FH) the influence of the apolipoprotein E (apoE) polymorphism on pre-treatment plasma lipid levels and on the response to treatment with simvastatin was studied. The apoE phenotype distribution did not differ significantly between the FH group and a sample group of the Dutch population. Differences in pre-treatment lipid levels were not related to the apoE polymorphism in this FH population. After 12 weeks use of a daily dose of 40 mg simvastatin, the plasma total cholesterol, low density lipoprotein (LDL)-cholesterol and plasma triglyceride levels were reduced on average by 33%, 38% and 19%, respectively. At the same time high density lipoprotein (HDL)-cholesterol concentration increased on average by 7%. In the combined FH patient group (males and females) a considerable interindividual variation in response to simvastatin was observed, but was not related to the apoE polymorphism. However, considering males and females separately, we found that female FH patients with the apoE3E3 phenotype responded better on simvastatin treatment with respect to LDL-cholesterol than male FH patients with the apoE3E3 phenotype.

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Year:  1990        PMID: 2390138     DOI: 10.1016/0021-9150(90)90134-5

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


  9 in total

1.  Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews.

Authors:  R Durst; R Colombo; S Shpitzen; L B Avi; Y Friedlander; R Wexler; F J Raal; D A Marais; J C Defesche; M Y Mandelshtam; M J Kotze; E Leitersdorf; V Meiner
Journal:  Am J Hum Genet       Date:  2001-04-17       Impact factor: 11.025

2.  Role of rs3846662 and HMGCR alternative splicing in statin efficacy and baseline lipid levels in familial hypercholesterolemia.

Authors:  Valerie Leduc; Lucienne Bourque; Judes Poirier; Robert Dufour
Journal:  Pharmacogenet Genomics       Date:  2016-01       Impact factor: 2.089

Review 3.  Simvastatin. A reappraisal of its pharmacology and therapeutic efficacy in hypercholesterolaemia.

Authors:  G L Plosker; D McTavish
Journal:  Drugs       Date:  1995-08       Impact factor: 9.546

4.  Exploratory data analysis of hyperlipidemia on the Macintosh: software tools for analysis of biochemical, clinical, and genetic variables in 1677 consecutive lipid clinic patients.

Authors:  V Bhushan; M J Malloy; M M Engler; M B Engler; D Drown; J P Kane
Journal:  J Med Syst       Date:  1993-08       Impact factor: 4.460

Review 5.  Benefits and risks of simvastatin in patients with familial hypercholesterolaemia.

Authors:  Pedro Mata; Rodrigo Alonso; Juan Badimón
Journal:  Drug Saf       Date:  2003       Impact factor: 5.606

Review 6.  Pharmacogenetics of lipid diseases.

Authors:  Jose M Ordovas
Journal:  Hum Genomics       Date:  2004-01       Impact factor: 4.639

7.  Factors explaining the gender disparity in lipid-lowering treatment goal attainment rate in Chinese patients with statin therapy.

Authors:  Rui Zhang; Liancheng Zhao; Lirong Liang; Gaoqiang Xie; Yangfeng Wu
Journal:  Lipids Health Dis       Date:  2012-05-29       Impact factor: 3.876

8.  Treatment of dyslipidemia: genetic interactions with diet and drug therapy.

Authors:  J M Ordovas; E J Schaefer
Journal:  Curr Atheroscler Rep       Date:  1999-07       Impact factor: 5.967

9.  [Apolipoprotein E polymorphism in the population of northern Morocco: frequency and effect on lipid parameters].

Authors:  Fatiha Benyahya; Amina Barakat; Naima Ghailani; Mohcine Bennani
Journal:  Pan Afr Med J       Date:  2013-08-31
  9 in total

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