Sidjanin Duska J, McCarty Catherine A, Patchett Richard, Smith Edward, Wilke Russell A
Medical College of Wisconsin, Department of Cell Biology, Neurobiology and Anatomy, Milwaukee, WI, USA, Tel.: +1 414 456 7810; ; E-mail:
Per Med. 2008;5(4):377-385. doi: 10.2217/17410541.5.4.377.
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 beta-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.
青光眼是全球第二大致盲原因。原发性青光眼的危险因素是眼压升高。局部用β受体阻滞剂价格低廉,被广泛用于降低眼压。遗传变异性被认为是导致局部用β受体阻滞剂疗效和安全性存在个体差异的原因。本综述总结了在β肾上腺素能受体(ADRB1、ADRB2和ADRB3)中已鉴定出的具有临床意义的多态性。还讨论了CYP2D6基因多态性的影响。尽管候选基因方法在我们对青光眼治疗反应的遗传基础的理解上取得了重大进展,但大多数药物反应涉及大量基因,每个基因都包含多个多态性。全基因组关联研究可能会产生一组与青光眼结局相关的更全面的多态性。了解与局部用β受体阻滞剂个体反应变异性相关的遗传机制可能会以更低的成本推进个体化治疗。