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
[61]   A common β1-adrenergic receptor polymorphism (Arg389Gly) affects blood pressure response to β-blockade [J].
Sofowora, GG ;
Dishy, V ;
Muszkat, M ;
Xie, HG ;
Kim, RB ;
Harris, PA ;
Prasad, HC ;
Byrne, DW ;
Nair, UB ;
Wood, AJJ ;
Stein, CM .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2003, 73 (04) :366-371
[62]   Amiodarone N-deethylation by CYP2C8 and its variants, CYP2C8*3 and CYP2C8 P404A [J].
Soyama, A ;
Hanioka, N ;
Saito, Y ;
Murayama, N ;
Ando, M ;
Ozawa, S ;
Sawada, J .
PHARMACOLOGY & TOXICOLOGY, 2002, 91 (04) :174-178
[63]   Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia [J].
Splawski, I ;
Timothy, KW ;
Tateyama, M ;
Clancy, CE ;
Malhotra, A ;
Beggs, AH ;
Cappuccio, FP ;
Sagnella, GA ;
Kass, RS ;
Keating, MT .
SCIENCE, 2002, 297 (5585) :1333-1336
[64]   Chemosensitivity prediction by transcriptional profiling [J].
Staunton, JE ;
Slonim, DK ;
Coller, HA ;
Tamayo, P ;
Angelo, MJ ;
Park, J ;
Scherf, U ;
Lee, JK ;
Reinhold, WO ;
Weinstein, JN ;
Mesirov, JP ;
Lander, ES ;
Golub, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) :10787-10792
[65]  
STEARNS RA, 1995, DRUG METAB DISPOS, V23, P207
[66]   Genetic analysis of the human cytochrome P450 CYP2C9 locus [J].
Stubbins, MJ ;
Harries, LW ;
Smith, G ;
Tarbit, MH ;
Wolf, CR .
PHARMACOGENETICS, 1996, 6 (05) :429-439
[67]   CYP2C9 Ile359 and Leu359 variants:: enzyme kinetic study with seven substrates [J].
Takanashi, K ;
Tainaka, H ;
Kobayashi, K ;
Yasumori, T ;
Hosakawa, M ;
Chiba, K .
PHARMACOGENETICS, 2000, 10 (02) :95-104
[68]   Influence of cytochrome P-450CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment [J].
Taube, J ;
Halsall, D ;
Baglin, T .
BLOOD, 2000, 96 (05) :1816-1819
[69]   Effects of endothelial nitric oxide synthase, α-adducin, and other candidate gene polymorphisms on blood pressure response to hydrochlorothiazide [J].
Turner, ST ;
Chapman, AB ;
Schwartz, GL ;
Boerwinkle, E .
AMERICAN JOURNAL OF HYPERTENSION, 2003, 16 (10) :834-839
[70]   Digoxin pharmacokinetics and MDR1 genetic polymorphisms [J].
Verstuyft, C ;
Schwab, M ;
Schaeffeler, E ;
Kerb, R ;
Brinkmann, U ;
Jaillon, P ;
Funck-Brentano, C ;
Bacquemont, L .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2003, 58 (12) :809-812