14-Year Incidence, Progression, and Visual Morbidity of Age-Related MaculopathyThe Copenhagen City Eye Study
Abstract
Purpose To describe the 14-year incidence of age-related maculopathy (ARM) lesions and the related visual loss.Design Population-based cohort study.Participants Nine hundred forty-six residents (age range, 60-80 years) of Copenhagen participated in the study from 1986 through 1988. Excluding participants who had died since baseline, 359 persons (97.3% of survivors) were reexamined from 2000 through 2002.Methods Participants underwent extensive ophthalmologic examinations. Age-related maculopathy lesions were determined by grading color fundus photographs from the examinations using a modified Wisconsin Age-Related Maculopathy Grading System.Main outcome measures Incidence of drusen type and size, pigmentary abnormalities, pure geographic atrophy, exudative ARM, visual impairment, and blindness.Results The 14-year incidences of early and late ARM were 31.5% and 14.8%, respectively. Individuals 75 to 80 years of age at baseline had significantly (P< or =0.05) higher 14-year incidences of the following lesions than those aged 60 to 64 years: medium or large drusen (> or =125 microm; 34.2% vs. 12.8%, respectively), soft drusen (45.2% vs. 21.4%), pigmentary abnormalities (31.4% vs. 17.0%), pure geographic atrophy (17.4% vs. 1.0%), and exudative ARM (23.3% vs. 5.7%). Severe drusen type, large drusen, and retinal pigmentary abnormalities at baseline were important predictors of incident late ARM. The 14-year incidences of visual impairment (<20/40 but >20/200) or legal blindness from late ARM were 6.0% and 3.4%, respectively. Late ARM caused 35.7% of all visual impairment and 66.7% of all blindness.Conclusions There is a high incidence of ARM lesions in this elderly white population. Severe drusen type and size or a combination of drusen and pigmentary abnormalities significantly increases the risk of developing late ARM, the most frequent cause of legal blindness in this population.
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Serum triglycerides are not associated with late AMD.
“Neither the two prospective cohort studies [27,46] (RR 1.0; 95% CI 0.77 - 1.30) nor the cross-sectional studies[28,52,60] (OR 1.08; 95% CI 0.89 - 1.30), found an association between serum triglycerides and late AMD (data not shown).”
From Clinical risk factors for age-related macular degeneration: a systematic review and meta-analysis (2010) · cites this paper as [27]
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References 53 · Cited by 131
- Authors
- BUCH, H., NIELSEN, N., VINDING, T., JENSEN, G., PRAUSE, J., & LACOUR, M.
- Affiliations
- Rigshospitalet (DK)
- University of Copenhagen (DK)
- Corresponding author
- BUCH, H
- Venue
- Ophthalmology
- Publisher
- Elsevier BV
- Published
- 2005-05
- Volume
- 112
- Issue
- 5
- Pages
- 787-798
- ISSN
- 0161-6420 (ISSN-L)
- OpenAlex
- W2088432960
- Cited by
- 131
- References
- 53
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 6 · 2023: 2 · 2022: 4 · 2021: 7 · 2020: 9 · 2019: 6 · 2018: 5 · 2017: 10 · 2016: 4 · 2015: 8 · 2014: 8 · 2013: 7 · 2012: 8
- FWCI
- 6.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Ophthalmology (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Topics
- Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Retinal Imaging and Analysis
- Health Sciences › Medicine › Ophthalmology › Ocular Diseases and Behçet’s Syndrome
- Keywords
- age-related maculopathy, drusen, geographic atrophy, neovascular age-related macular degeneration, visual impairment, legal blindness, incidence, disease progression, risk factors, older adults, visual morbidity, age-related macular degeneration
- MeSH terms
- Aged, Aged, 80 and over, Denmark, Female, Follow-Up Studies, Humans, Macular Degeneration, Male, Middle Aged, Retinitis Pigmentosa, Risk Factors, Vision Disorders, Visual Acuity, Retinal Drusen, Incidence, Disease Progression, Persons with Visual Disabilities
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