Literature DB >> 11931715

Pharmacogenetics of Lipid-lowering Therapies.

Jose M Ordovas1, Haiqing Shen.   

Abstract

Cardiovascular disease is associated with nonmodifiable risk factors such as age, gender, and genetic background, and with modifiable risk factors such as lipid concentrations. Lowering serum lipid levels has been demonstrated to slow the progression of, or even induce regression in, atherosclerosis. However, like any other drug treatment, the magnitude of plasma lipid responses to drug therapies varies considerably among individuals. Pharmacogenetics provides the experimental basis to understand the variability in response to drugs as a function of the individual genetic makeup. Information from small clinical trials reveals that several candidate genes may hold some promise in our quest to predict individual success to hypolipemic drug treatment. However, the current clinical relevance of this knowledge is quite limited due to the small effects observed for each of the genetic markers examined. Future progress in this area will be driven by studying gene-gene and gene-treatment interactions in much larger patient populations.

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Year:  2002        PMID: 11931715     DOI: 10.1007/s11883-002-0018-2

Source DB:  PubMed          Journal:  Curr Atheroscler Rep        ISSN: 1523-3804            Impact factor:   5.113


  47 in total

Review 1.  Gene-diet interaction and plasma lipid response to dietary intervention.

Authors:  J M Ordovas
Journal:  Curr Atheroscler Rep       Date:  2001-05       Impact factor: 5.113

2.  Interactions between angiotensin-I converting enzyme insertion/deletion polymorphism and response of plasma lipids and coronary atherosclerosis to treatment with fluvastatin: the lipoprotein and coronary atherosclerosis study.

Authors:  A J Marian; F Safavi; L Ferlic; J K Dunn; A M Gotto; C M Ballantyne
Journal:  J Am Coll Cardiol       Date:  2000-01       Impact factor: 24.094

Review 3.  State-of-the-art update and review: clinical trials of lipid-lowering agents.

Authors:  P O Kwiterovich
Journal:  Am J Cardiol       Date:  1998-12-17       Impact factor: 2.778

Review 4.  Matrix metalloproteinases and cardiovascular disease.

Authors:  C M Dollery; J R McEwan; A M Henney
Journal:  Circ Res       Date:  1995-11       Impact factor: 17.367

5.  Interethnic variability in human drug responses.

Authors:  D A Evans; H L McLeod; S Pritchard; M Tariq; A Mobarek
Journal:  Drug Metab Dispos       Date:  2001-04       Impact factor: 3.922

Review 6.  Genetic diversity in the matrix metalloproteinase family. Effects on function and disease progression.

Authors:  A M Henney; S Ye; B Zhang; S Jormsjö; C Whatling; P Eriksson; A Hamsten
Journal:  Ann N Y Acad Sci       Date:  2000-05       Impact factor: 5.691

Review 7.  Pharmacogenomics: the inherited basis for interindividual differences in drug response.

Authors:  W E Evans; J A Johnson
Journal:  Annu Rev Genomics Hum Genet       Date:  2001       Impact factor: 8.929

8.  Baseline characteristics of subjects in the Lipoprotein and Coronary Atherosclerosis Study (LCAS) with fluvastatin.

Authors:  J A Herd; M S West; C Ballantyne; J Farmer; A M Gotto
Journal:  Am J Cardiol       Date:  1994-05-26       Impact factor: 2.778

9.  Impact of apolipoprotein E polymorphism in determining interindividual variation in total cholesterol and low density lipoprotein cholesterol in Hispanics and non-Hispanic whites.

Authors:  M I Kamboh; C E Aston; R E Ferrell; R F Hamman
Journal:  Atherosclerosis       Date:  1993-01-25       Impact factor: 5.162

10.  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

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  1 in total

Review 1.  Genetics, the environment, and lipid abnormalities.

Authors:  Jose M Ordovas; And Haiqing Shen
Journal:  Curr Cardiol Rep       Date:  2002-11       Impact factor: 2.931

  1 in total

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