News Releases

December 4, 2008

Clinical Trial Aims to Help Those with Macular Degeneration Find New Way of Seeing

• The brain’s ability to reorganize itself can help compensate for vision loss.
• For those with age-related macular degeneration, behavioral improvements can lead to change in brain activity.
• A Phase 2 trial at Emory and Georgia Institute of Technology will study how to use remaining vision and design new rehabilitation therapies.

RetinaATLANTA - The brain’s remarkable ability to reorganize itself to compensate for vision loss, the ability called plasticity, may be the key in helping those with age-related macular degeneration (AMD) see better. This theory is the impetus behind a study between Emory Eye Center and the Georgia Institute of Technology (Psychology). Patients who have retinal damage because of AMD sometimes begin to see by using other parts of the intact retina. By “training” these patients to focus on using those good retinal cells, they may experience increased visual acuity.

Susan Primo, OD, MPH, of Emory Eye Center, says the Phase 2 portion of the clinical trial “Age-Related Macular Degeneration and Cortical Reorganization” will help bridge the knowledge gap between cortical plasticity and visual function.

“Results from these studies will begin to provide answers for how behavioral improvements in AMD patients can lead to changes in underlying brain activity and, most importantly, how we can influence those changes to maximize use of remaining vision,” Primo says. “Once this link is made, clinicians and healthcare engineers can use the information to design and implement rehabilitation therapies and technologies that will expedite efficient use of fixation strategies ultimately fostering cortical reorganization.”

Age–related macular degeneration is the leading cause of blindness in the elderly, accounting for 10 million people who have reduced vision in the United States (Research to Prevent Blindness). AMD is a disease associated with aging that gradually destroys sharp, central vision. Central vision is needed for seeing objects clearly and for common daily tasks such as reading and driving. People in middle-age have about a 2 percent risk of getting AMD, but this risk increases to nearly 30 percent in those over age 75. More than 200,000 develop AMD each year in this country.

“Visual rehabilitation is entering an exciting area of research that expands our current understanding of neuroplasticity of the visual system,” says Timothy W. Olsen, director of Emory Eye Center and a retina specialist. “Findings from this study and others may help us understand the tremendous capacity of our central nervous system, especially as it relates to sensory deficits. Combining expertise of the Emory Eye Center with Georgia Tech opens exciting new opportunities in vision research.”

Phase 1 of the study appears in the December edition of the journal Restorative Neurology and Neuroscience (Restor Neurol Neurosci. 2008;26(4-5):391-402.) Phase 1 of the trial at Emory involved seven patients, and the Phase 2 portion at Emory will have 10 patients. The goal will be to study hundreds of patients in the near future. Results will be disseminated in late 2009.

Funding is provided through the Health Systems Institute (HSI) Seed Grant, a collaboration between Georgia Institute of Technology and Emory University/Children’s Healthcare of Atlanta/Egleston. The HSI Seed Grant supports collaborative and interdisciplinary research projects that will help stimulate innovative healthcare research and promote improvements in healthcare. The seed grant awards are specifically designed to provide funding for novel projects that demonstrate a high potential for enhanced diagnostic capabilities of diseases, lead to new inventions that yield new patents, licenses and/or commercial products, lead to high quality peer-reviewed publications and those with high potential to leverage seed funding into extra-mural support.

Media contact: Joy Bell, 404-778-3711

Photo caption: Small yellowish deposits known as drusen are seen forming under the retina blurring the sharp central area of vision or macula. Individual drusen, coalesce forming larger areas of damage. Blood vessels growing up from below the retina leak blood under the retina. Pressure from these pockets of blood, damage the light sensing cells, destroying the ability to see straight ahead.

Photo credit:  National Eye Institute, National Institutes of Health


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