Preservation of ganglion cell layer neurons in age-related macular degeneration

Citation
Ne. Medeiros et Ca. Curcio, Preservation of ganglion cell layer neurons in age-related macular degeneration, INV OPHTH V, 42(3), 2001, pp. 795-803
Citations number
44
Categorie Soggetti
da verificare
Journal title
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
ISSN journal
01460404 → ACNP
Volume
42
Issue
3
Year of publication
2001
Pages
795 - 803
Database
ISI
SICI code
0146-0404(200103)42:3<795:POGCLN>2.0.ZU;2-J
Abstract
PURPOSE. TO determine the number of neurons remaining in the ganglion cell layer (GCL) of eyes with nonexudative and exudative age-related macular deg eneration (NEAMD and EXAMD, respectively) in relation to photoreceptor loss in the same retinas. METHODS. The study design was a clinicopathologic correlation. Macular phot oreceptors and GCL neurons were counted in unstained retinal wholemounts fr om eyes of patients with NEAMD (n = 6) and EXAMD (n = 5) and from control p atients without grossly visible drusen or pigmentary change (n = 15; age ra nge, 60-95 years). The authors determined the percentage of counting sites with significant cell loss relative to control eyes and for photoreceptors, the percentage of sites where rod or cone loss predominated. The total num bers of cones, rods, and GCL neurons were determined within the 6-mm-diamet er macula. Fellow eyes were prepared for light and electron microscopic eva luation of retinal pigment epithelium and Bruch's membrane disease. RESULTS. EXAMD eyes had severe photoreceptor loss. The total number of macu lar photoreceptors in NEAMD eyes was similar to the number in control eyes, despite moderate loss in the parafovea. In 9 of 11 AMD eyes, rod loss was greater than cone loss at the same locations. EXAMD eyes had 47% fewer GCL neurons than control eyes. GCL neurons in NEAMD eyes did not differ signifi cantly from control eyes. CONCLUSIONS. Interventions targeted at the outer retina early in the progre ssion of neovascular disease should benefit from the full age-appropriate c omplement of GCL neurons.