PMID- 24135755 OWN - NLM STAT- MEDLINE DCOM- 20140124 LR - 20211021 IS - 1552-5783 (Electronic) IS - 0146-0404 (Print) IS - 0146-0404 (Linking) VI - 54 IP - 12 DP - 2013 Nov 15 TI - Cone structure imaged with adaptive optics scanning laser ophthalmoscopy in eyes with nonneovascular age-related macular degeneration. PG - 7498-509 LID - 10.1167/iovs.13-12433 [doi] AB - PURPOSE: To evaluate cone spacing using adaptive optics scanning laser ophthalmoscopy (AOSLO) in eyes with nonneovascular AMD, and to correlate progression of AOSLO-derived cone measures with standard measures of macular structure. METHODS: Adaptive optics scanning laser ophthalmoscopy images were obtained over 12 to 21 months from seven patients with AMD including four eyes with geographic atrophy (GA) and four eyes with drusen. Adaptive optics scanning laser ophthalmoscopy images were overlaid with color, infrared, and autofluorescence fundus photographs and spectral domain optical coherence tomography (SD-OCT) images to allow direct correlation of cone parameters with macular structure. Cone spacing was measured for each visit in selected regions including areas over drusen (n = 29), at GA margins (n = 14), and regions without drusen or GA (n = 13) and compared with normal, age-similar values. RESULTS: Adaptive optics scanning laser ophthalmoscopy imaging revealed continuous cone mosaics up to the GA edge and overlying drusen, although reduced cone reflectivity often resulted in hyporeflective AOSLO signals at these locations. Baseline cone spacing measures were normal in 13/13 unaffected regions, 26/28 drusen regions, and 12/14 GA margin regions. Although standard clinical measures showed progression of GA in all study eyes, cone spacing remained within normal ranges in most drusen regions and all GA margin regions. CONCLUSIONS: Adaptive optics scanning laser ophthalmoscopy provides adequate resolution for quantitative measurement of cone spacing at the margin of GA and over drusen in eyes with AMD. Although cone spacing was often normal at baseline and remained normal over time, these regions showed focal areas of decreased cone reflectivity. These findings may provide insight into the pathophysiology of AMD progression. (ClinicalTrials.gov number, NCT00254605). FAU - Zayit-Soudry, Shiri AU - Zayit-Soudry S AD - Department of Ophthalmology, University of California at San Francisco, San Francisco, California. FAU - Duncan, Jacque L AU - Duncan JL FAU - Syed, Reema AU - Syed R FAU - Menghini, Moreno AU - Menghini M FAU - Roorda, Austin J AU - Roorda AJ LA - eng SI - ClinicalTrials.gov/NCT00254605 GR - P30 EY002162/EY/NEI NIH HHS/United States GR - R01 EY014375/EY/NEI NIH HHS/United States GR - EY014375/EY/NEI NIH HHS/United States GR - EY002162/EY/NEI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20131115 PL - United States TA - Invest Ophthalmol Vis Sci JT - Investigative ophthalmology & visual science JID - 7703701 SB - IM MH - Aged MH - Disease Progression MH - Female MH - Fluorescein Angiography MH - Follow-Up Studies MH - Geographic Atrophy/*diagnosis MH - Humans MH - Male MH - Middle Aged MH - Ophthalmoscopy MH - Retinal Cone Photoreceptor Cells/*pathology MH - Retinal Drusen/*diagnosis MH - Tomography, Optical Coherence/*methods MH - Visual Acuity PMC - PMC3832216 OTO - NOTNLM OT - adaptive optics OT - age-related macular degeneration OT - cones OT - scanning laser ophthalmoscopy EDAT- 2013/10/19 06:00 MHDA- 2014/01/25 06:00 PMCR- 2014/05/01 CRDT- 2013/10/19 06:00 PHST- 2013/10/19 06:00 [entrez] PHST- 2013/10/19 06:00 [pubmed] PHST- 2014/01/25 06:00 [medline] PHST- 2014/05/01 00:00 [pmc-release] AID - iovs.13-12433 [pii] AID - 10.1167/iovs.13-12433 [doi] PST - epublish SO - Invest Ophthalmol Vis Sci. 2013 Nov 15;54(12):7498-509. doi: 10.1167/iovs.13-12433.