Neuroprotection in glaucoma: recent advances and clinical translation

被引:48
|
作者
Guymer, Chelsea [1 ]
Wood, John P. M. [1 ]
Chidlow, Glyn [1 ]
Casson, Robert J. [1 ]
机构
[1] Univ Adelaide, South Australian Inst Ophthalmol, Ophthalm Res Lab, WS7062-46,Level 7,Adelaide Hlth & Med Sci Bldg, Adelaide, SA 5000, Australia
来源
关键词
bioenergetics; clinical translation; glaucoma; neuroprotection; retinal ganglion cell; OPEN-ANGLE GLAUCOMA; RETINAL GANGLION-CELLS; CILIARY NEUROTROPHIC FACTOR; GENOME-WIDE ASSOCIATION; OPTIC-NERVE HEAD; OXIDATIVE STRESS; INTRAOCULAR-PRESSURE; STEM-CELLS; COMMON VARIANTS; ETHYL PYRUVATE;
D O I
10.1111/ceo.13336
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Intraocular pressure (IOP) reduction is currently the only evidence-based treatment strategy for glaucoma. However, IOP control in some individuals is challenging. Despite optimal treatment, a significant proportion of individuals will progress, with loss of visual field, loss of driving vision and impaired quality of life. A new modality that could augment current treatment and reduce the rate of neurodegeneration to preserve vision throughout life would be a major breakthrough. A vast number of studies have reported effective neuroprotection in animal models of glaucoma; however, translation to the clinic remains a major hurdle. Herein, we explore the therapeutic advancements in non-IOP-dependent neuroprotection research based upon potential pathogenic mechanisms and propose strategies to improve the clinical translation of neuroprotective research in glaucoma.
引用
收藏
页码:88 / 105
页数:18
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