Sears Avery E, Bernstein Paul S, Cideciyan Artur V, Hoyng Carel, Charbel Issa Peter, Palczewski Krzysztof, Rosenfeld Philip J, Sadda SriniVas, Schraermeyer Ulrich, Sparrow Janet R, Washington Ilyas, Scholl Hendrik P N
Department of Pharmacology, School of Medicine, Cleveland Center for Membrane and Structural Biology, Case Western Reserve University, Cleveland, OH, USA.
Moran Eye Center, University of Utah, Salt Lake City, UT, USA.
Transl Vis Sci Technol. 2017 Sep 14;6(5):6. doi: 10.1167/tvst.6.5.6. eCollection 2017 Sep.
Accumulation of fluorescent metabolic byproducts of the visual (retinoid) cycle is associated with photoreceptor and retinal pigment epithelial cell death in both Stargardt disease and atrophic (nonneovascular) age-related macular degeneration (AMD). As a consequence of this observation, small molecular inhibitors of enzymes in the visual cycle were recently tested in clinical trials as a strategy to protect the retina and retinal pigment epithelium in patients with atrophic AMD. To address the clinical translational needs for therapies aimed at both diseases, a workshop organized by the Foundation Fighting Blindness was hosted by the Department of Pharmacology at Case Western Reserve University on February 17, 2017, at the Tinkham Veale University Center, Cleveland, OH, USA. Invited speakers highlighted recent advances in the understanding of the pathophysiology of Stargardt disease, in terms of its clinical characterization and the development of endpoints for clinical trials, and discussed the comparability of therapeutic strategies between atrophic age-related macular degeneration (AMD) and Stargardt disease. Investigators speculated that reducing the concentrations of visual cycle precursor substances and/or their byproducts may provide valid therapeutic options for the treatment of Stargardt disease. Here we review the workshop's presentations in the context of published literature to help shape the aims of ongoing research endeavors and aid the development of therapies for Stargardt disease.
在斯塔加特病和萎缩性(非新生血管性)年龄相关性黄斑变性(AMD)中,视觉(视黄醛)循环的荧光代谢副产物的积累与光感受器和视网膜色素上皮细胞死亡有关。基于这一观察结果,视觉循环中酶的小分子抑制剂最近在临床试验中进行了测试,作为保护萎缩性AMD患者视网膜和视网膜色素上皮的一种策略。为满足针对这两种疾病的治疗方法的临床转化需求,2017年2月17日,由抗击失明基金会组织的一次研讨会在美国俄亥俄州克利夫兰市廷卡姆·维尔大学中心的凯斯西储大学药理学系举办。受邀演讲者强调了在斯塔加特病病理生理学理解方面的最新进展,包括其临床特征以及临床试验终点的制定,并讨论了萎缩性年龄相关性黄斑变性(AMD)和斯塔加特病治疗策略的可比性。研究人员推测,降低视觉循环前体物质及其副产物的浓度可能为斯塔加特病的治疗提供有效的治疗选择。在此,我们结合已发表的文献回顾该研讨会的报告内容,以帮助明确正在进行的研究工作的目标,并助力斯塔加特病治疗方法的开发。