Pharmacogenetics of ophthalmic topical β-blockers

被引:12
作者
Sidjanin, Duska J. [1 ,2 ]
McCarty, Catherine A. [3 ]
Patchett, Richard [3 ]
Smith, Edward [2 ]
Wilke, Russell A. [2 ,3 ,4 ,5 ]
机构
[1] Med Coll Wisconsin, Dept Cell Biol Neurobiol & Anat, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Human & Mol Genet Ctr, Milwaukee, WI 53226 USA
[3] Marshfield Clin Fdn Med Res & Educ, Marshfield, WI 54449 USA
[4] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
[5] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
关键词
D O I
10.2217/17410541.5.4.377
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glaucoma is the second leading cause of blindness worldwide. The primary glaucoma risk factor is elevated intraocular pressure. Topical beta-blockers are affordable and widely used to lower intraocular pressure. Genetic variability has been postulated to contribute to interpersonal differences in efficacy and safety of topical beta-blockers. This review summarizes clinically significant polymorphisms that have been identified in the p-adrenergic receptors (ADRB1, ADRB2 and ADRB3). The implications of polymorphisms in CYP2D6 are also discussed. Although the candidate-gene approach has facilitated significant progress in our understanding of the genetic basis of glaucoma treatment response, most drug responses involve a large number of genes, each containing multiple polymorphisms. Genome-wide association studies may yield a more comprehensive set of polymorphisms associated with glaucoma outcomes. An understanding of the genetic mechanisms associated with variability in individual responses to topical beta-blockers may advance individualized treatment at a lower cost.
引用
收藏
页码:377 / 385
页数:9
相关论文
共 65 条
[51]  
STEWART WC, 1987, ARCH OPHTHALMOL-CHIC, V115, P853
[52]   Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21 [J].
Stoilov, I ;
Akarsu, AN ;
Sarfarazi, M .
HUMAN MOLECULAR GENETICS, 1997, 6 (04) :641-647
[53]   Identification of a gene that causes primary open angle glaucoma [J].
Stone, EM ;
Fingert, JH ;
Alward, WLM ;
Nguyen, TD ;
Polansky, JR ;
Sunden, SLF ;
Nishimura, D ;
Clark, AF ;
Nystuen, A ;
Nichols, BE ;
Mackey, DA ;
Ritch, R ;
Kalenak, JW ;
Craven, ER ;
Sheffield, VC .
SCIENCE, 1997, 275 (5300) :668-670
[54]   Mutations in the TIGR gene in familial primary open-angle glaucoma in Japan [J].
Suzuki, Y ;
Shirato, S ;
Taniguchi, F ;
Ohara, K ;
Nishimaki, K ;
Ohta, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (05) :1202-1204
[55]   Pharmacogenetics of the human beta-adrenergic receptors [J].
Taylor, M. R. G. .
PHARMACOGENOMICS JOURNAL, 2007, 7 (01) :29-37
[56]   Association between β-adrenergic receptor polymorphisms and their G- protein-coupled receptors with body mass index and obesity in women:: a report from the NHLBI-sponsored WISE study [J].
Terra, SG ;
McGorray, SP ;
Wu, R ;
McNamara, DM ;
Cavallari, LH ;
Walker, JR ;
Wallace, MR ;
Johnson, BD ;
Merz, CNB ;
Sopko, G ;
Pepine, CJ ;
Johnson, JA .
INTERNATIONAL JOURNAL OF OBESITY, 2005, 29 (07) :746-754
[57]   β-2 adrenoceptor genetic variation is associated with genetic predisposition to essential hypertension:: The Bergen Blood Pressure Study [J].
Timmermann, B ;
Mo, R ;
Luft, FC ;
Gerdts, E ;
Busjahn, A ;
Omvik, P ;
Li, GH ;
Schuster, H ;
Wienker, TF ;
Hoehe, MR ;
Lund-Johansen, P .
KIDNEY INTERNATIONAL, 1998, 53 (06) :1455-1460
[58]   GENETIC POLYMORPHISMS OF THE BETA(2)-ADRENERGIC RECEPTOR IN NOCTURNAL AND NONNOCTURNAL ASTHMA - EVIDENCE THAT GLY16 CORRELATES WITH THE NOCTURNAL PHENOTYPE [J].
TURKI, J ;
PAK, J ;
GREEN, SA ;
MARTIN, RJ ;
LIGGETT, SB .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1635-1641
[59]  
VANBUSKIRK EM, 1980, OPHTHALMOLOGY, V87, P447
[60]  
WAX MB, 1987, INVEST OPHTH VIS SCI, V28, P420