Pharmacogenomics in cardiovascular medicine

被引:2
作者
Carlquist, JF [1 ]
Anderson, JL [1 ]
机构
[1] Univ Utah, Sch Med, Salt Lake City, UT USA
关键词
pharmacogenomics; cardiovascular drugs; single nucleotide polymorphisms;
D O I
10.1002/ddr.10355
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The completion of the Human Genome Project (HGP) holds promise for further insight into how genetic differences contribute to an individual's response to a medicine(s). Even before the completion of the HGP, cardiovascular medicine was thrust into the arena of pharmacogenomics by the observation that many drugs, cardiovascular and noncardiovascular, promote cardiac arrhythmias. It is now recognized that these adverse responses as well as beneficial responses to cardiovascular medicines can be influenced by alterations in the genes for metabolizing enzymes, drug transporters, and drug targets. To the present, much basic information regarding gene-drug interactions has accumulated, but translation to clinical care has been slow. It is anticipated that the pace of clinical cardiovascular pharmacogenomics will increase as the result of better-designed studies and technological advances. The final adoption of this area of investigation into clinical practice will also be influenced by financial, psychosocial, and legal factors. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:180 / 190
页数:11
相关论文
共 80 条
[71]   A pharmacogenetic approach to blood pressure in Lyon hypertensive rats - A chromosome 2 locus influences the response to a calcium antagonist [J].
Vincent, M ;
Samani, NJ ;
Gauguier, D ;
Thompson, JR ;
Lathrop, GM ;
Sassard, J .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (08) :2000-2006
[72]   Torsade de pointes with an antihistamine metabolite: Potassium channel blockade with desmethylastemizole [J].
Vorperian, VR ;
Zhou, ZF ;
Mohammad, S ;
Hoon, TJ ;
Studenik, C ;
January, CT .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1996, 28 (06) :1556-1561
[73]  
Walker DK, 1996, DRUG METAB DISPOS, V24, P447
[74]   Using genome-wide mapping in the mouse to identify genes that influence drug response [J].
Watters, JW ;
McLeod, HL .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2003, 24 (02) :55-58
[75]  
Weiss S. T., 2001, Pharmacogenomics Journal, V1, P157
[76]   Reduced inhibition by abciximab in platelets with the PIA2 polymorphism [J].
Wheeler, GL ;
Braden, GA ;
Bray, PF ;
Marciniak, SJ ;
Mascelli, MA ;
Sane, DC .
AMERICAN HEART JOURNAL, 2002, 143 (01) :76-82
[77]   MECHANISM OF THE CARDIOTOXIC ACTIONS OF TERFENADINE [J].
WOOSLEY, RL ;
CHEN, YW ;
FREIMAN, JP ;
GILLIS, RA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 269 (12) :1532-1536
[78]   Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes [J].
Yang, P ;
Kanki, H ;
Drolet, B ;
Yang, T ;
Wei, J ;
Viswanathan, PC ;
Hohnloser, SH ;
Shimizu, W ;
Schwartz, PJ ;
Stanton, M ;
Murray, KT ;
Norris, K ;
George, AL ;
Roden, DM .
CIRCULATION, 2002, 105 (16) :1943-1948
[79]   Validation of methods for CYP2C9 genotyping:: Frequencies of mutant alleles in a Swedish population [J].
Yasar, Ü ;
Eliasson, E ;
Dahl, ML ;
Johansson, I ;
Ingelman-Sundberg, M ;
Sjoqvist, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 254 (03) :628-631
[80]   Common hepatic lipase gene promoter variant determines clinical response to intensive lipid-lowering treatment [J].
Zambon, A ;
Deeb, SS ;
Brown, BG ;
Hokanson, JE ;
Brunzell, JD .
CIRCULATION, 2001, 103 (06) :792-798