a Department of Ophthalmology, The Second Xiangya Hospital , Central South University , Changsha , China.
b Department of Ophthalmology, The Hamilton Eye Institute , The University of Tennessee Health Science Center , Memphis , TN , USA.
Expert Opin Investig Drugs. 2017 Oct;26(10):1103-1114. doi: 10.1080/13543784.2017.1369042. Epub 2017 Aug 24.
Age-related macular degeneration (AMD) is the leading cause of vision loss among the elderly. Atrophic AMD, including early, intermediate and geographic atrophy (GA), accounts for ~90% of all cases. It is a multifactorial degeneration characterized by chronic inflammation, oxidative stress and aging components. Although no FDA-approved treatment yet exists for the late stage of atrophic AMD, multiple pathological mechanisms are partially known and several promising therapies are in various stages of development. Areas covered: Underlying mechanisms that define atrophic AMD will help provide novel therapeutic targets that will address this largely unmet clinical need. The purpose of this paper is to review current promising drugs that are being evaluated in clinical trials. Because no pharmacological treatments are currently available for late stage of atrophic AMD, any new therapy would have extensive market potential. Expert opinion: The number of AMD patients is predicted to increase to ~30 million worldwide by 2020. In response to this enormous unmet clinical need, new promising therapies are being developed and evaluated in clinical trials. We propose that the assessment of novel interventions will also need to consider the genotypes of participants, as the benefit may be determined by polymorphisms in an individual's genetic background.
年龄相关性黄斑变性(AMD)是老年人视力丧失的主要原因。萎缩性 AMD,包括早期、中期和地图状萎缩(GA),占所有病例的~90%。它是一种多因素变性,其特征为慢性炎症、氧化应激和衰老成分。尽管目前还没有 FDA 批准的治疗晚期萎缩性 AMD 的方法,但部分已知的多种病理机制和几种有前途的疗法正在不同阶段的开发中。
定义萎缩性 AMD 的潜在机制将有助于提供新的治疗靶点,以满足这一主要未满足的临床需求。本文的目的是回顾正在临床试验中评估的当前有前途的药物。由于目前尚无治疗晚期萎缩性 AMD 的药物,任何新疗法都将具有广泛的市场潜力。
预计到 2020 年,全球 AMD 患者人数将增加到~3000 万。为了应对这一巨大的未满足的临床需求,新的有前途的疗法正在临床试验中进行开发和评估。我们提出,对新干预措施的评估还需要考虑参与者的基因型,因为个体遗传背景中的多态性可能决定其获益。