Macular Degeneration Research
Krysten M. Farjo, Ph.D.
University of Oklahoma Health Sciences Center
Oklahoma City, OK, United States
Title: A Novel Visual Cycle Inhibitor to Treat Macular Degeneration
Non-Technical Title: Developing a New Therapeutic for Macular Degeneration
Duration: July 1, 2012 - June 30, 2014
Award Type: Standard
Award Amount: $100,000
Many types of macular degeneration are initiated and maintained by the accumulation of toxic vitamin A derivatives in the retina. Dr. Krysten Farjo and colleages are focusing on developing a new therapeutic agent to reduce the formation of toxic vitamin A derivatives by inhibiting vitamin A uptake into the retina. The ultimate goal is to develop a drug that could be used to slow and prevent vision loss in patients with macular degeneration.
There are currently no treatment options for patients with juvenile-onset Stargardt's macular degeneration (STGD) or early-stage age-related macular degeneration (dry AMD). STGD and dry AMD are both initiated and perpetuated by the accumulation of toxic vitamin A derivatives in the form of non-degradable permanent lipofuscin retinal deposits, fatty deposits that may lead to drusen*. Lipofuscin accumulates slowly during the normal aging process, but in STGD and dry AMD patients lipofuscin levels are 2 to 5 times higher than in the rest of the population, indicating that lipofuscin formation is abnormally accelerated in both diseases.
It has been established that toxic vitamin A derivatives are generated in the special cycle of metabolism used by the retina to continuously detect light and observe visual images; this metabolic cycle has been named the "visual cycle." Studies over the past decade have shown that slight to moderate inhibition of the visual cycle can significantly reduce the formation of toxic vitamin A derivatives and prevent vision loss in mice with STGD and dry AMD. Moreover, clinical studies have shown that the visual cycle can be partially inhibited without severely impairing normal vision in human patients. Despite these promising results, the existing visual cycle inhibitors are chemicals that may have undesirable side effects, including the potential to inflict further damage on the retina.
Dr. Krysten Farjo and colleagues are developing a new non-chemical visual cycle inhibitor that is designed to reduce vitamin A uptake in the retina and thereby reduce visual cycle activity and the generation of toxic vitamin A derivatives. They have already identified several new inhibitor candidates and are currently focused on improving the effectiveness of these candidates to increase their therapeutic potential. If successful, this research has a good chance of developing a safe and effective visual cycle inhibitor for the treatment of STGD and dry AMD, fulfilling an unmet and critical need.
*Drusen are yellow (waste products from metabolism) that form and accumulate under the retina, between the retinal pigmented epithelium (RPE) layer and the Bruch's membrane, the blood-retina barrier that supports the retina.
Dr. Krysten Farjo is an Assistant Professor of Research in the Department of Physiology at the University of Oklahoma Health Sciences Center. As a native Oklahoman, she also completed her doctoral studies and postdoctoral training at the University of Oklahoma Health Sciences Center, within the departments of Cell Biology and Endocrinology, respectively. Farjo's research focuses on the regulation of vitamin A transport, metabolism, and function, particularly in the context of retinal health and disease. Her research team is largely devoted to understanding the role of vitamin A metabolism in the pathogenesis of age-related macular degeneration (AMD) and a juvenile-onset form of macular degeneration known as Stargardt disease (STGD). Farjo's research team will utilize the BrightFocus Macular Degeneration Research Award to develop a novel therapeutic mechanism to manipulate vitamin A transport in the retina. This research has direct implications for the treatment of AMD and STGD, as both forms of macular degeneration are initiated by the accumulation of toxic vitamin A derivatives in the retina. Farjo was previously awarded a grant from another organization to begin this research project and is now able to build upon these studies thanks to the support of BrightFocus donors.