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      Impairments in Dark Adaptation are Associated with Age-Related Macular Degeneration Severity and Reticular Pseudodrusen

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          Abstract

          Purpose

          We investigate whether ocular and person-based characteristics are associated with dark adaptation (DA) measured using the AdaptRx™ device (Apeliotus Technologies, Atlanta, GA).

          Design

          Cross-sectional, single-center, observational study.

          Participants

          116 participants >50 years with a range in age-related macular degeneration (AMD) severity.

          Methods

          Participants underwent best-corrected visual acuity (BCVA) testing, ophthalmoscopic examination and multimodal imaging. Presence of reticular pseudodrusen (RPD) was assessed by masked grading of fundus images and confirmed with OCT. Eyes were also graded for AMD features (drusen, pigmentary changes, late AMD) to generate a person-based AMD severity groups. One eye was designated the study eye for DA testing using the AdaptRx™ device. Nonparametric statistical testing was performed on all comparisons.

          Main Outcome Measure

          The primary outcome of this study was the rod-intercept time (RIT) which is defined as the time for a participant's visual sensitivity to recover to a stimulus intensity of 5 × 10 −3 cd/m 2 (a decrease of 3 log units), or until a maximum test duration of 40 minutes was reached.

          Results

          A total of 116 study eyes in 116 participants (mean age=75.4±9.4 years, 58% female) were analyzed. Increased RIT was significantly associated with increasing age ( r=0.34, p=0.0002), decreasing BCVA ( r=−0.54, p<0.0001), pseudophakia ( p=0.03), decreasing subfoveal choroidal thickness ( r=−0.27, p=0.003). Study eyes with RPD (15/116, 13%) had a significantly greater mean RIT compared to eyes without RPD in any AMD severity group ( p<0.02 for all comparisons) with 80% reaching the DA test ceiling.

          Conclusion

          Impairments in DA increase with age, worse visual acuity, presence of RPD, AMD severity and decreased subfoveal choroidal thickness. Analysis of covariance found the multivariable model that best fit our data included age, AMD group, and presence of RPD (R 2=0.56) with the presence of RPD conferring the largest parameter estimate.

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          Author and article information

          Journal
          7802443
          6266
          Ophthalmology
          Ophthalmology
          Ophthalmology
          0161-6420
          1549-4713
          5 August 2015
          04 August 2015
          October 2015
          01 October 2016
          : 122
          : 10
          : 2053-2062
          Affiliations
          National Eye Institute, NIH Bethesda, Maryland 20892, USA.
          Author notes
          [1 ] Correspondence and Reprint requests to: Catherine Cukras, MD, PhD Division of Epidemiology and Clinical Research and Ophthalmic Genetics and Visual Function Branch National Eye Institute National Institute of Health Bethesda, Maryland 20892 Tel: (301) 435-5061. Fax: (301) 402-1214 cukrasc@ 123456nei.nih.gov
          Article
          PMC4836058 PMC4836058 4836058 nihpa705241
          10.1016/j.ophtha.2015.06.023
          4836058
          26253372
          12a04061-fe37-437b-8e5c-45f7962d1d1e
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