Author Affiliations: Scheie Eye Institute (Drs Ying and Maguire and Mss Alexander and Martin), University of Pennsylvania, Philadelphia; and Charlotte Eye, Ear, Nose, and Throat, Charlotte, North Carolina (Dr Antoszyk).Group Information: A list of the CAPT Research Group appears in the eAppendix.
To describe characteristics of the Age-Related Eye Disease Study (AREDS) 9-step severity scale applied to participants in the Complications of Age-related Macular Degeneration Prevention Trial (CAPT).
Eligibility criteria for CAPT required 10 or more large (≥125 μm) drusen in each eye. Readers graded baseline photographs from all participants and all follow-up photographs from 402 untreated eyes. Drusen and pigment characteristics were used to assign the AREDS scale score. Choroidal neovascularization was identified from fluorescein angiograms. Geographic atrophy involving the macular center was identified from color photographs.
Among 1001 untreated eyes, 90% were at steps 5 to 7 at baseline. The 5-year incidence of advanced age-related macular degeneration (AMD) increased with each step from 8% (step 4) to 40% (steps 8 and 9 combined). These rates were similar to those reported in AREDS. Among 261 eyes with all 5 annual photograph gradings available and without progression to advanced AMD, 55% of eyes had scores that indicated improvement at least once. Before progression to advanced AMD, only 32% of 141 eyes either went through step 8 or 9 or had an increase of 2 or more steps from baseline.
The AREDS 9-step severity scale was predictive of development of advanced AMD. The AREDS scale has deficiencies as a surrogate outcome for progression to advanced AMD.
Population-based epidemiological studies1,2 and cohort studies involving clinical trial participants3- 5 have demonstrated that the characteristics of early and intermediate age-related macular degeneration (AMD), including drusen size, area, and pigment abnormalities, are strong risk factors for the progression to advanced AMD. The Age-Related Eye Disease Study (AREDS) recently developed a complicated 9-step AMD severity scale for eyes6 and a simplified 5-step severity scale for persons7 based on gradings of stereoscopic color photographs for drusen features and pigment abnormalities. The AREDS 9-step severity scale, which will be referred to as the AREDS scale, was developed with the intention
to provide baseline risk categories, to allow tracking of progression along the scale, and to define surrogate outcomes for progression to advanced AMD.6(p1484)
The AREDS scale was found to be highly associated with progression to advanced AMD in AREDS participants, with eyes classified in the lowest category at baseline having a 5-year risk of progression of less than 1% and eyes in the highest category having a risk of approximately 50%. The AREDS investigators performed an initial assessment of longitudinal changes in the AREDS scale score by examining the pattern of 4 scale steps ordered in time (baseline and 2, 4, and 5 years of follow-up) in a subgroup of 366 eyes that had changed between baseline and 5 years by at least 3 steps. In 334 eyes (91%), the AREDS scale step at 5 years was higher than at baseline and in 259 (78%) of these eyes there were no reversals toward improvement at 2 and 4 years. On the basis of these analyses, the AREDS investigators concluded that progression on the AREDS scale may prove to be useful as a surrogate for progression to advanced AMD.
Before any severity scale is adopted for clinical or research purposes, the risk estimates should be validated in an independent sample.8 However, to our knowledge, the AREDS scale has not been validated in any population-based cohorts or in other large groups of people with early or intermediate AMD. In addition, much additional information is needed about the characteristics of the changes in scale step over time in eyes with and without progression to advanced AMD before changes in the AREDS scale score can be considered as a surrogate outcome measure.
The Complications of Age-related Macular Degeneration Prevention Trial (CAPT) was a multicenter randomized clinical trial in a large cohort of participants (n = 1052). Each participant was followed up for at least 5 years to observe the development of advanced AMD (about 20% of eyes developed advanced AMD within 5 years), and color photographs and fluorescein angiograms were obtained at least yearly and graded following a protocol similar to AREDS. Thus, the CAPT data provide a unique opportunity to validate risk estimates associated with the AREDS scale and to assess patterns of severity scale score changes over time in eyes with and without subsequent progression to advanced AMD.
Details of the design and methods have been reported elsewhere5,9,10; only major features related to this article are described herein. A total of 1052 participants were enrolled into CAPT between May 1999 and March 2001. One eye of each participant was randomized to laser treatment, with the contralateral eye assigned to observation. CAPT eligibility criteria specified that each eye had 10 or more large drusen (≥125 μm in diameter). Neither eye was to have evidence of choroidal neovascularization (CNV), serous pigment epithelial detachment, geographic atrophy (GA) within 500 μm of foveal center or total area more than 1 Macular Photocoagulation Study disc area (DA), or other ocular conditions that were likely to compromise visual acuity or contraindicate application of laser treatment.
At the initial visit and annual visits thereafter, certified photographers adhering to a standardized protocol for field definition and image sequencing took stereoscopic, color fundus photographs on film and a fluorescein angiogram on film, with frames from each eye. Color photographs were taken also at 6 months. Fluorescein angiograms were taken also when there were signs or symptoms of CNV. All photographic images were graded independently by 2 trained readers in the CAPT Reading Center who later openly discussed their discrepancies to arrive at consensus. The fundus features described in the grading included number of drusen, largest drusen size, drusen area, drusen confluence, GA, focal hyperpigmentation, and retinal pigment epithelium depigmentation. Because the initial grading of fundus photographs was slightly different from the AREDS grading with respect to categorization of drusen size, drusen area, GA, and pigmentation abnormalities, we regraded the photographs for AMD characteristics needed for determination of the AREDS scale step, following the AREDS grading protocol.11 The regrading involved all the baseline photographs of treated and untreated eyes, all follow-up photographs of a random sample of 261 untreated eyes without progression to advanced AMD, and 141 untreated eyes with progression to advanced AMD after 12 months' follow-up.
Readers in the CAPT Reading Center also evaluated the follow-up images for the presence of CNV and GA involving the center of the macula (CGA). Fluorescein angiograms were used to identify CNV, defined as expansion or persistent staining of an area of hyperfluorescence as the time from injection increased. Geographic atrophy was considered present when the color photographs showed an area of atrophy of the retinal pigment epithelium with a diameter of at least 250 μm with 2 of the following 3 features: visible choroidal vessels, sharp edges, and a more or less circular shape. Geographic atrophy involving the center of the macula was defined as development of GA involving the center of the macula. Evaluation of CGA was not performed after an eye developed CNV because the neovascular complex and subsequent scarring often occupied or obscured the retinal area most likely to develop GA.
The institutional review board associated with each clinical center approved the study protocol and written informed consent was obtained from each participant. Data management was compliant with Health Insurance Portability and Accountability Act guidelines. The conduct of the clinical trial adhered to the tenets of the Declaration of Helsinki.
Statistical analyses were restricted to the data from the untreated eye of each CAPT participant. A computer algorithm was used to assign an AREDS scale step to each eye derived from the gradings of the photograph, following the definition of the AREDS scale.6 A descriptive analysis was performed to examine the distribution of the AREDS severity scale steps at baseline. Crude 5-year incidence rates and their 95% confidence intervals (CIs) of advanced AMD (CNV or CGA separately and combined) by baseline AREDS scale step were calculated. These rates were compared with those reported by the AREDS investigators using χ2 tests or Fisher exact tests (when an expected number in a cell was <5) of proportions. These tests did not account for the intereye correlation between the outcomes of the 2 eyes of the same participant used in the AREDS estimates. Accounting for the positive correlation requires the use of raw data from each eye from AREDS and would increase the P values. Longitudinal patterns of the AREDS scale steps were examined with descriptive statistics. All data analyses were performed in SAS 9.1 (SAS Institute Inc, Cary, North Carolina).
At baseline, the drusen area and pigmentation abnormalities necessary for application of the AREDS scale could be determined from fundus photographs in 1018 untreated eyes (96.8%) of 1052 CAPT participants. Among these, 1001 eyes (98.3%) met the drusen eligibility criteria (at least 10 large drusen >125 μm) and were free of advanced AMD (CNV or CGA) at baseline. The distribution of baseline AREDS scale steps from 1001 eyes is shown in Figure 1. About half (52%) of the eyes had a severity step of 7 and more than a quarter (28%) of eyes had a step of 6, indicating that the majority of eyes had drusen area more than 0.5 DA or drusen area more than 0.028 DA with the definite presence of increased pigment or depigmentation. The steps 8 (ie, drusen area >0.5 DA and depigmentation area of 0.056-0.5 DA or depigmentation area >0.5 DA) and 9 (ie, presence of noncentral GA) were uncommon (<5%) among the CAPT eyes.
The distribution of Age-Related Eye Disease Study (AREDS) 9-step severity scale scores among Complications of Age-related Macular Degeneration Prevention Trial untreated eyes at baseline (N = 1001 eyes).
Among 1001 participants with an eligible untreated eye at baseline, 866 (87%) survived and completed 5-year follow-up. Within 5 years of follow-up, 178 eyes (20.5%) developed advanced AMD, either CNV (12.6%) or CGA (8.4%). Four eyes (0.5%) developed CNV after developing CGA. The crude 5-year incidence of advanced AMD increased with the AREDS 9-step scale score, 8% (95% CI, 3%-21%) for step 4, 9% (95% CI, 5%-16%) for step 5, 19% (95% CI, 15%-25%) for step 6, 23% (95% CI, 20%-27%) for step 7, and 40% (95% CI, 26%-55%) for steps 8 and 9 combined. The CAPT estimated 5-year incidence rates were higher than the AREDS estimates for eyes with baseline steps of 4 to 6 and lower for eyes with baseline steps of 7 to 9 (Table 1) (Figure 2); however, none of these differences were statistically significant (P > .05). The 5-year incidence of CNV and incidence of CGA each also increased with higher steps on the AREDS scale. In both CAPT and AREDS eyes, the incidence of CGA was very low (<1%) for baseline steps 4 or 5 and increased sharply at steps 7 and higher. Those with baseline steps 4 to 6 were more likely to develop CNV than CGA, those with step 7 were approximately equally likely to develop CNV as CGA, and those with steps 8 or 9 were more likely to develop CGA than CNV.
The crude 5-year incidence of advanced age-related macular degeneration (AMD) by Age-Related Eye Disease Study (AREDS) scale step in Complications of Age-related Macular Degeneration Prevention Trial (CAPT) eyes and AREDS eyes.
The progression of the AREDS scale step over 5 years was assessed among a randomly selected subset of 261 of 644 untreated eyes (41%) without the development of advanced AMD during 5-year follow-up and with all 5 annual gradings available. Among these 261 eyes, 47 eyes (18%) maintained the same scale step through 5 years and 71 eyes (27%) increased 1 or more steps without reversals (Table 2), including 12 eyes (5%) with scale steps that increased more than 2 steps within 5 years. The scale step decreased at least once between 2 annual photographs during the 5 years of follow-up in the remaining 143 eyes (55%). Among these eyes, 13 eyes (5%) decreased 1 or more steps without reversals, including 1 eye that decreased more than 2 steps; 107 eyes (41%) fluctuated within 1 or 2 steps, and 23 eyes (9%) fluctuated more than 2 steps. At baseline or during the 5-year course of follow-up, 73 eyes (28%) reached the scale steps of 8 or 9, and 82 of 249 eyes (33%) ever had at least a 2-step increase from baseline scale step of 7 or less.
To assess the pattern of scale steps before an eye developed advanced AMD, baseline and annual follow-up AREDS scale steps were analyzed in 141 untreated eyes that developed advanced AMD (CNV or CGA) within 5 years and had at least 1 annual grading available. The median number of annual gradings available before the development of advanced AMD was 3, with 24 eyes (17%) having only 1 annual grading. Of these 141 eyes, 52 eyes (37%) maintained the baseline scale step until development of advanced AMD (Table 2); however, 17 of these eyes had only 1 annual grading. Thirty-six eyes (26%) showed a stepwise increase, including 23 eyes (16%) that increased by 2 or more steps. The scale step decreased at least once between 2 annual photographs before development of advanced AMD in the remaining 53 eyes (38%). Among these eyes, 16 eyes (11%) showed a stepwise decrease in scale steps, while 37 eyes (26%) fluctuated over time, including 9 eyes (6%) that changed more than 2 steps. Prior to progression to advanced AMD, 41 eyes (29%) reached the highest AREDS scale steps of 8 or 9, and 33 eyes (26%) had a 2-step increase or greater from baseline among 129 eyes that had a baseline scale step of 7 or less.
The pattern of AREDS scale steps over time was also examined within type of advanced AMD (Table 2). The median number of annual gradings available before development of advanced AMD was 3 for both those developing CNV and those developing CGA. A higher proportion of eyes developing CGA went through steps 8 or 9 than eyes developing CNV (56% vs 14%; P < .001) (Table 2). Also, increases of 2 or more steps from baseline were more common in eyes that later developed CGA than eyes that later developed CNV (44% vs 17%; P = .002).
The large number and long-term follow-up of CAPT participants along with the similarity of the CAPT photograph grading protocol to the AREDS protocol provided an excellent opportunity to validate the AREDS 9-step AMD severity scale in an independent sample. As in AREDS, the risk of advanced AMD among CAPT participants increased with each successive step of the AREDS scale. Furthermore, the estimates of the level of risk for each of the steps among CAPT participants were relatively close to the AREDS estimates (Figure 2). Thus, the CAPT data validate the predictive power of the AREDS 9-step severity scale for the progression to advanced AMD for the range of steps present in CAPT patients at baseline (4-9). Although the AREDS simplified 5-step severity scale for persons has been recently validated in a population-based Blue Mountains cohort,2 to our knowledge, ours is the first study to validate the AREDS complicated 9-step scale for eyes in a large, independent cohort.
Decreases in the AREDS scale step over time were common in CAPT participants (Table 2). Among eyes that did not progress to advanced AMD and had all 5 follow-up annual photographs, the AREDS scale step for 55% of eyes either decreased from baseline and did not later increase (5%) or decreased and later increased (50%). Some fluctuation in steps may be due to grading variation, because the grading-regrading agreement for drusen and pigmentary characteristics was moderate to substantial in both CAPT and AREDS, with the percentage of exact agreement ranging from 78% to 94% in CAPT5 and 63% to 78% in AREDS.11 However, fluctuation greater than 2 steps is less likely due to grading variation, as grading-regrading agreement within 2 steps of the AREDS scale was 94% in the AREDS study6; instead, it is more likely due to the true disappearance of drusen or pigment. In 1973, Gass12 noted that drusen appear and disappear naturally, a finding that has been confirmed by others.13,14 Sarks et al15,16 have described the natural progression of soft drusen as growth to confluence, leading to a small retinal pigment epithelial detachment, then fading to leave behind pigment mottling and/or atrophy in some, but not all, cases. A recent report based on 95 AREDS eyes that developed GA during AREDS follow-up provided results consistent with the Sarks et al description. Klein et al17 noted that the development of GA was nearly always preceded by regression of drusen and pigment followed by the appearance of hypopigmentation. On the AREDS scale, smaller drusen area and disappearance of pigment results in a lower step unless there is a simultaneous increase in the area of hypopigmentation.
In their report on the construction of the 9-step severity scale, AREDS investigators concluded that the AREDS scale might prove useful as a surrogate outcome. This conclusion was based on the assessment of changes in scale steps over time (baseline, years 2, 4, and 5) in 366 eyes that had changed by at least 3 steps between baseline and 5 years.6 One possible candidate for a surrogate outcome measure would be a change in step greater than the variation attributable to grading error (ie, ≥2 steps). Our detailed path analyses of CAPT eyes showed that 33% of eyes that did not progress to advanced AMD within 5 years had such a change, while such a change occurred in 26% of eyes that did progress to advanced AMD. To accommodate the eyes with severity scale steps of 8 or 9 that did not have the opportunity to increase 2 or more steps, another possible candidate for a surrogate outcome is the change to steps 8 or 9 or an increase of 2 or more steps from baseline. We found that about 36% of eyes reached scale steps 8 or 9 or ever had increases of 2 or more steps from baseline, yet did not progress to advanced AMD within 5 years. More than two-thirds of eyes neither reached the most severe scale steps (steps 8 or 9) nor had a substantial increase in scale step (≥2 steps) from baseline before eyes progressed to advanced AMD. Thus, using change in the AREDS scale step as a surrogate outcome would not decrease the time to observing an outcome relative to development of advanced AMD in the majority of eyes. This, along with the fact that fluctuations in scale step often occur over time, compromises the usefulness of change in step on the severity scale as a surrogate outcome for progression of AMD.18
The pattern of scale steps over time was different between eyes that later developed CNV and those that developed CGA. Before progression to CGA, about 50% of eyes ever had reached the steps 8 or 9 or had experienced an increase of 2 or more steps from baseline; this occurred in less than 20% of eyes that later progressed to CNV. This may be because the AREDS 9-step scale algorithm assigns step 9 to eyes with noncentral GA and step 8 to eyes whose predominant feature is hypopigmentation. This suggests that the AREDS 9-step severity scale is better used to monitor the development of CGA than of CNV.
The CAPT study is limited by the homogeneity of CAPT participants. The eligibility criteria of CAPT required each eye to have at least 10 large drusen (≥125 μm in diameter, 0.0069 DA in area); thus, at baseline the majority of eyes (>80%) in CAPT participants were at steps 6 or 7, and no eyes were at steps 1, 2, or 3 (drusen area <0.056 DA). This fact prevents us from assessing and validating the 5-year incidence rate for steps 1, 2, and 3. Also, because steps 8 and 9 were uncommon (<5%) in both CAPT and AREDS participants, we lack power to reliably validate the incidence rate of advanced AMD for these steps.
In conclusion, we validated the predictive power of the AREDS 9-step severity scale for advanced AMD in CAPT participants. The severity scale provides convenient risk categories for patients with AMD. However, our longitudinal path analyses show that change in the AREDS scale step has deficiencies in serving as a surrogate outcome for progression to advanced AMD.
Correspondence: Gui-shuang Ying, PhD, CAPT Coordinating Center, University of Pennsylvania, 3535 Market St, Ste 700, Philadelphia, PA 19104-3309 (email@example.com).
Submitted for Publication: December 3, 2008; final revision received February 3, 2009; accepted February 9, 2009.
Financial Disclosure: None reported.
Funding/Support: Supported by grants EY012211, EY012261, and EY012279 from the National Eye Institute, National Institutes of Health, Department of Health and Human Services.
Previous Presentation: Presented in part at the meeting of the Association for Research and Vision in Ophthalmology; April 28, 2008; Fort Lauderdale, Florida.
Additional Information: The eAppendix is available at http://www.archophthalmol.com.
Thank you for submitting a comment on this article. It will be reviewed by JAMA Ophthalmology editors. You will be notified when your comment has been published. Comments should not exceed 500 words of text and 10 references.
Do not submit personal medical questions or information that could identify a specific patient, questions about a particular case, or general inquiries to an author. Only content that has not been published, posted, or submitted elsewhere should be submitted. By submitting this Comment, you and any coauthors transfer copyright to the journal if your Comment is posted.
* = Required Field
Disclosure of Any Conflicts of Interest*
Indicate all relevant conflicts of interest of each author below, including all relevant financial interests, activities, and relationships within the past 3 years including, but not limited to, employment, affiliation, grants or funding, consultancies, honoraria or payment, speakers’ bureaus, stock ownership or options, expert testimony, royalties, donation of medical equipment, or patents planned, pending, or issued. If all authors have none, check "No potential conflicts or relevant financial interests" in the box below. Please also indicate any funding received in support of this work. The information will be posted with your response.
Some tools below are only available to our subscribers or users with an online account.
Download citation file:
Web of Science® Times Cited: 2
Customize your page view by dragging & repositioning the boxes below.
Enter your username and email address. We'll send you a link to reset your password.
Enter your username and email address. We'll send instructions on how to reset your password to the email address we have on record.
Athens and Shibboleth are access management services that provide single sign-on to protected resources. They replace the multiple user names and passwords necessary to access subscription-based content with a single user name and password that can be entered once per session. It operates independently of a user's location or IP address. If your institution uses Athens or Shibboleth authentication, please contact your site administrator to receive your user name and password.