IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


(Investigative Ophthalmology and Visual Science. 2008;49:55-65.)
© 2008 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.06-1048

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dimitrov, P. N.
Right arrow Articles by Vingrys, A. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dimitrov, P. N.
Right arrow Articles by Vingrys, A. J.

Measuring Rod and Cone Dynamics in Age-Related Maculopathy

Peter N. Dimitrov,1 Robyn H. Guymer,1 Andrew J. Zele,2,3 Andrew J. Anderson,4 and Algis J. Vingrys4

1From the Centre for Eye Research Australia, Department of Ophthalmology, The University of Melbourne, East Melbourne, Victoria, Australia; the 2School of Optometry and the 3Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia; and the 4Department of Optometry and Vision Sciences, The University of Melbourne, Parkville, Victoria, Australia.

PURPOSE. A cathode-ray-tube (CRT) monitor–based technique was used to isolate clinically significant components of dark adaptation. The utility of the technique in identifying adaptation abnormalities in eyes with age-related maculopathy (ARM) is described.

METHODS. A CRT dark adaptometer was developed to assess cone and rod recovery after photopigment bleach. The following measures were obtained: cone recovery rate (Rc; in decades per minute) and absolute threshold (Tfc; log candelas per square meter), rod recovery rate (Rr; decades per minute), and rod–cone transition (rod–cone break [RCB], in minutes). These components were isolated by appropriately selecting stimulus size, stimulus location, pigment bleach, and test duration and by coupling the CRT with judiciously selected neutral-density (ND) filters. The protocol was developed by using 5 young observers and was tested on 27 subjects with ARM in the study eye and 22 age-matched control subjects.

RESULTS. The parameters necessary for effective isolation of cone and early phase rod dark adaptation were a 2.6 ND filter (for a standard CRT monitor, 0.08–80 cd · m–2 luminance output); a 4° foveated, 200-ms, achromatic spot; ~30% pigment bleaching; and a 30-minute test duration. These settings returned obvious rod and cone recovery curves in control and ARM eyes that were compatible with conventional test methods and identified 93% of participants with ARM as having delayed dynamics in at least one of the parameters. Cone recovery dynamics were significantly slower in the ARM group when compared with age-matched control subjects (Rc, 0.99 ± 0.35 vs. 2.63 ± 0.61 decades · min–1, P < 0.0001). Three of the 27 eyes with ARM did not achieve RCB during the allowed duration (30 minutes). The remaining eyes with ARM (n = 24) exhibited a significant delay in rod recovery (Rr, ARM, 0.16 ± 0.03 vs. controls, 0.22 ± 0.02 decades · min–1, P < 0.0001) and the average time to RCB (±SD) in the ARM group was significantly longer than in the control subjects (19.12 ± 5.17 minutes vs. 10.40 ± 2.49 minutes, P < 0.0001).

CONCLUSIONS. The CRT dark-adaptation technique described in this article is an effective test for identifying abnormalities in cone and rod recovery. Slowed cone and rod recovery and a delayed RCB were evident in the eyes with ARM. The test method is potentially useful for clinical intervention trials in which ARM progression is monitored.








HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by the Association for Research in Vision and Ophthalmology