Cited by 1,062Retinal Diseases and TreatmentsRetinal Imaging and AnalysisOcular Diseases and Behçet’s Syndrome

The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.

Prevalence of Age-related Maculopathy in Australia

Abstract

Purpose To examine the prevalence of age-related maculopathy (drusen and retinal pigmentary abnormalities) and end-stage age-related macular degeneration lesions (neovascular maculopathy or geographic atrophy) in a defined older Australian urban population.Subjects All noninstitutionalized residents 49 years of age or older who were identified in a door-to-door census of two postcode areas west of Sydney, Australia.Methods All participants received a detailed eye examination, including stereoscopic photographs of each macula. Two trained graders used the Wisconsin Age-related Maculopathy Grading System to assess the presence and severity of typical lesions.Results A marked age-related increase in all typical lesions of age-related maculopathy and macular degeneration was observed. End-stage age-related macular degeneration was present in 1.9% of the population, rising from 0% among people younger than 55 years of age to 18.5% among those 85 years of age or older. Soft drusen were found in 13.3% of people, with distinct drusen more frequent than indistinct soft drusen. Retinal pigmentary abnormalities were found in 12.6% of people. For end-stage lesions and soft drusen, females had higher age-specific prevalence rates than males, whereas retinal pigmentary abnormalities were more frequent in males, although most of these differences were not significant. Prevalence rates for all lesions were lower (statistically significant for retinal pigmentary abnormalities and soft drusen) than for the United States Beaver Dam Eye Study which examined a similar population.Conclusions These data provide detailed prevalence rates for most components of ARM in an Australian population and reinforce the Beaver Dam Eye Study findings for the relative age-specific frequency of age-related macular degeneration components.

Overview

Integrity signals

Registry

Crossref · 10.1016/s0161-6420(95)30846-9

Cites

24 of 24 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Age is the strongest risk factor for age-related macular degeneration; all population-based studies confirm that the prevalence of age-related macular degeneration increases with age in white individuals.

    “Age is the strongest risk factor for age-related macular degeneration; all population-based studies confirm that the prevalence of age-related macular degeneration increases with age in white individuals.3,22–27”

    From Age-related macular degeneration (2008) · cites this paper as [22]

  • The 5-year incidence of soft drusen in the Reykjavik Eye Study was similar to that of the Beaver Dam Eye Study and the Blue Mountains Eye Study.

    “The 5-y incidence of soft drusen in the Reykjavik Eye Study, a population-based epidemiological study of individuals aged 50 y and older [28,29], was found to be similar to that of the Beaver Dam Eye Study in the US [30], and the Blue Mountains Eye Study in Australia [31].”
  • Neovascular AMD outnumbers GA by approximately three to one in the Beaver Dam Eye Study and the Blue Mountains Eye Study.

    “Neovascular AMD outnumbers GA by approximately three to one in both the Beaver Dam Eye Study and the Blue Mountains Eye Study.”

Citations

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Metadata

Authors
Mitchell, P., Smith, W., Attebo, K., & Wang, J. J.
Affiliations
The University of Sydney (AU)
Corresponding author
Mitchell, Paul
Venue
Ophthalmology
Publisher
Elsevier BV
Published
1995-10
Volume
102
Issue
10
Pages
1450-1460
ISSN
0161-6420 (ISSN-L)
OpenAlex
W1882214116
Cited by
1,062
References
24
Citations by year
2026: 10 · 2025: 8 · 2024: 16 · 2023: 23 · 2022: 21 · 2021: 20 · 2020: 28 · 2019: 16 · 2018: 30 · 2017: 35 · 2016: 29 · 2015: 48 · 2014: 52 · 2013: 60 · 2012: 42
FWCI
26.73
Type
journal article
Language
en
Open access
closed
Locations
  • Ophthalmology (publishedVersion)
  • PubMed (publishedVersion)
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, age-related macular degeneration, drusen, geographic atrophy, neovascular age-related macular degeneration, prevalence, older adults, sex differences, age-specific prevalence, Australian population
MeSH terms
Aged, Aged, 80 and over, Australia, Female, Humans, Macular Degeneration, Male, Middle Aged, Reproducibility of Results, Observer Variation, Prevalence, Age Distribution

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review