AMD, which is the third most prevalent cause of vision loss worldwide and is twice as common as Alzheimer disease in older persons, affects the central part of the retina causing changes to central vision leading to sight loss.
The research study recently published in Investigative Ophthalmology and Visual Science, found that retinal pigment epithelial (RPE) cells removed directly from the eye can reproduce all the major known elements of drusen, the hallmark extracellular deposit of AMD, when the cells are grown on specific surfaces.
The cell culture model developed confirms that RPE cells in early AMD are functional and that the conditions of the so called Bruch’s membrane, the layer in the eye on which RPE cells grow, is key for the formation of drusen deposits. These then increase the risk of developing later stages of AMD.
This cell culture model is the most comprehensive developed so far and will provide an insight into disease progression and the best route to early treatment before vision loss occurs.
Dr Imre Lengyel, from the Centre for Experimental (CEM) at Queen’s University, who conducted the mineralomics analysis on the study, said: “We expect that this reproducible and valid model system will be important in determining what molecules in drusen and what changes in RPE cells can cause advancement to late stages of AMD.”
The elderly are the fastest growing segment of the population. New drug targets to help older persons maintain good vision and independent living are eagerly sought. This research will be an important milestone for patients with age-related macular degeneration, their families, and eye doctors.
Dr Christine Curcio, from the Department of Ophthalmology at University of Alabama, Birmingham, added: “Based on our experiments there is a whole new way to look at how drusen form and increase the risk of developing AMD. From this research study we now believe that drusen reduction is now a viable treatment goal.”
Matthew Pilgrim, PhD student at the Institute of Ophthalmology, University College London, who worked on the research project with Dr Lengyel, said: “There is no better education for a student than to be part of an important interdisciplinary project and learn about team science in addition to advanced microanalysis. Working on a project that is important for patients is very rewarding.”
The research has been funded by a number of international funding bodies including the European Union’s Horizon 2020 research and innovation program and Research to Prevent Blindness.
ENDS
Media inquiries to Zara McBrearty, Communications Office at Queen's University Belfast on Tel: 028 90 97 3259 or email [email protected]
Notes to Editor
1. The whitepaper is available to download here: http://iovs.arvojournals.org/article.aspx?articleid=2600542 2. Dr Imre Lengyel, from the Centre for Experimental Medicine at the School of Medicine, Dentistry and Biomedical Sciences at Queen’s University Belfast is available for interview. 3. The research has been funded by the “Eye-Risk”, a European Union’s Horizon 2020 research and innovation program under grant agreement No 634479, the Bill Brown Charitable Trust Senior Research Fellowship, Moorfields Eye Hospital Special Trustees, Mercer Fund from Fight for Sight, and Bright Focus Foundation in the UK. 4. The research has been funded by the National Institutes of Health, Department of Energy, International Retinal Research Foundation, EyeSight Foundation of Alabama, and Research to Prevent Blindness in the USA.
Journal Link: Investigative Ophthalmology and Visual Science
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