Cited by 186Retinal Diseases and TreatmentsRetinal Imaging and AnalysisRetinal Development and Disorders

Histologic Features of the Early Stages of Age-related Macular Degeneration

van der Schaft, Theo L., Mooy, Cornelia M., de Bruijn, Wim C., Oron, Frans G., Mulder, Paul G.H., de Jong, Paul T.V.M.·1992·Ophthalmology

Abstract

The age distribution, frequency, and correlation among histologic macular changes, including formation of a basal laminar deposit, drusen, and thickening and calcification of Bruch's membrane, were studied by light microscopy. The authors studied 182 unpaired postmortem human maculae from patients between 8 and 100 years of age. In addition, 45 maculae of contralateral eyes and the peripheral retina of 50 eyes were studied. In 92%, Bruch's membrane was thickened starting at age 19, and calcifications in this membrane were found in 59% starting at age 33. In 37% of the maculae, hard drusen were found starting at age 34. Soft drusen were found in 10% beginning at age 54. Basal laminar deposit was found in 39% of the maculae starting at age 40. All changes correlated strongly with age (P less than 0.0001). No sex differences were found. Fellow eyes showed similar aging changes (P less than 0.001). The presence of basal laminar deposit in the macula correlated with basal laminar deposit-like material in the peripheral retina (correlation coefficient, 0.39; P less than 0.003), whereas drusen in the macula correlated with drusen in the peripheral retina (correlation coefficient, 0.42; P = 0.001). Geographic atrophy was found in 6.6% of the eyes from subjects older than 70 years and subretinal neovascularization in 3.8%, especially in the maculae with basal laminar deposit.

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Crossref · 10.1016/s0161-6420(92)31982-7

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

  • BlinD are a more specific marker of AMD progression to late disease, and BlamD are a more reliable indicator of RPE atrophy and photoreceptor degeneration.

    “BlinD are a more specific marker of AMD progression to late disease, and BlamD are a more reliable indicator of RPE atrophy and photoreceptor degeneration (van der Schaft et al., 1992; Curcio and Millican, 1999; Sarks, 1976).”

    From Retinal ultrastructure of murine models of dry age-related macular degeneration (AMD) (2010) · cites this paper as van der Schaft et al., 1992

  • The presence of an inflammatory cell component at the site of breaks in Bruch's membrane strongly suggests that the immune system is intricately involved in disease progression.

    “The presence of an inflammatory cell component at the site of breaks in Bruch’s membrane strongly suggests that the immune system is intricately involved in disease progression (van der Schaft et al., 1992; Spraul and Grossniklaus, 1997; Anderson et al., 2002; Chan et al., 2008; Patel and Chan, 2008).”

    From Retinal ultrastructure of murine models of dry age-related macular degeneration (AMD) (2010) · cites this paper as van der Schaft et al., 1992

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References 22 · Cited by 186

Authors
van der Schaft, T. L., Mooy, C. M., de Bruijn, W. C., Oron, F. G., Mulder, P. G. H., & de Jong, P. T. V. M.
Affiliations
Erasmus University Rotterdam (NL)
Venue
Ophthalmology
Publisher
Elsevier BV
Published
1992-02
Volume
99
Issue
2
Pages
278-286
ISSN
0161-6420 (ISSN-L)
OpenAlex
W1967507509
Cited by
186
References
22
Citations by year
2026: 6 · 2025: 7 · 2024: 4 · 2023: 4 · 2022: 1 · 2021: 4 · 2020: 11 · 2019: 7 · 2018: 4 · 2017: 1 · 2016: 7 · 2015: 4 · 2014: 3 · 2013: 5 · 2012: 7
FWCI
8.76
Type
journal article
Language
en
Open access
closed
Locations
Ophthalmology (publishedVersion)
Topics
  • Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Retinal Imaging and Analysis
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
Keywords
age-related macular degeneration, drusen, basal laminar deposits, geographic atrophy, subretinal neovascularization, peripheral retina, histopathology

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