Literature DB >> 17270675

Fifteen-year cumulative incidence of age-related macular degeneration: the Beaver Dam Eye Study.

Ronald Klein1, Barbara E K Klein, Michael D Knudtson, Stacy M Meuer, Maria Swift, Ronald E Gangnon.   

Abstract

PURPOSE: To describe the 15-year cumulative incidence of signs of early and late age-related macular degeneration (AMD).
DESIGN: Population-based cohort study. PARTICIPANTS: We included 3917 persons, 43 to 86 years of age at the time of a baseline examination in 1988 through 1990 and with information collected in follow-up in 1993 through 1995, and/or 1998 through 2000, and/or 2003 through 2005.
METHODS: Grading of stereoscopic fundus photographs using the Wisconsin Age-Related Maculopathy Grading System. MAIN OUTCOME MEASURES: Cumulative incidence of drusen type and size, pigmentary abnormalities, geographic atrophy, and exudative AMD accounting for competing risk of death.
RESULTS: The 15-year cumulative incidence was 14.3% for early AMD (the presence of either soft indistinct drusen or the presence of pigmentary abnormalities together with any type of drusen) and 3.1% for late AMD (presence of exudative AMD or geographic atrophy). There was an increased incidence of AMD lesions with age (P<0.05). Individuals > or = 75 years of age at baseline had significantly (P<0.01) higher 15-year incidences of the following characteristics than people 43 to 54 years of age: larger drusen (125 mum in diameter, 24.1% vs 10.6%), soft indistinct drusen (18.7% vs 6.5%), retinal pigmentary abnormalities (20.2% vs 3.7%), exudative macular degeneration (4.4% vs 0.4%), and pure geographic atrophy (3.2% vs 0%). Controlling for age, compared with those with small numbers of only small hard drusen (1-2), those with large numbers of only hard drusen (> or =8) had an increased 15-year age-adjusted incidence of both soft indistinct drusen (16.3% vs 4.7%) and pigmentary abnormalities (10.6% vs 2.7%). Eyes with soft indistinct drusen or pigmentary abnormalities at baseline were more likely to develop late AMD at follow-up than eyes without these lesions (17.8% vs 1.2% and 12.9% vs 1.7%, respectively).
CONCLUSIONS: We document the long-term incidence of signs of AMD and a continuum from small hard drusen to late AMD in older persons in the population. The 15-year cumulative incidence of late AMD in people > or = 75 years of age (8%) indicates a public health problem of significant proportions because the United States population this age is expected to increase by 54% between 2005 and 2025.

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Mesh:

Year:  2007        PMID: 17270675     DOI: 10.1016/j.ophtha.2006.10.040

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  227 in total

1.  Drusen characterization with multimodal imaging.

Authors:  Richard F Spaide; Christine A Curcio
Journal:  Retina       Date:  2010-10       Impact factor: 4.256

2.  Intra and interobserver agreement in the classification of fundus autofluorescence patterns in geographic atrophy secondary to age-related macular degeneration.

Authors:  Marc Biarnés; Jordi Monés; Fabio Trindade; Jordi Alonso; Luis Arias
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2011-10-28       Impact factor: 3.117

3.  Treatment of geographic atrophy by the topical administration of OT-551: results of a phase II clinical trial.

Authors:  Wai T Wong; Waynekid Kam; Denise Cunningham; Molly Harrington; Keri Hammel; Catherine B Meyerle; Catherine Cukras; Emily Y Chew; Srinivas R Sadda; Frederick L Ferris
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-06-23       Impact factor: 4.799

Review 4.  [Clinical characteristics, progression and risk factors of geographic atrophy].

Authors:  C K Brinkmann; C Adrion; U Mansmann; S Schmitz-Valckenberg; F G Holz
Journal:  Ophthalmologe       Date:  2010-11       Impact factor: 1.059

5.  [Geographic atrophy in AMD].

Authors:  S Schmitz-Valckenberg; F G Holz
Journal:  Ophthalmologe       Date:  2010-11       Impact factor: 1.059

6.  Macular pigment density at the site of altered fundus autofluorescence.

Authors:  Simon Paul Rothenbuehler; Ute E K Wolf-Schnurrbusch; Sebastian Wolf
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2010-09-28       Impact factor: 3.117

7.  Angiogenic and Immunologic Proteins Identified by Deep Proteomic Profiling of Human Retinal and Choroidal Vascular Endothelial Cells: Potential Targets for New Biologic Drugs.

Authors:  Justine R Smith; Larry L David; Binoy Appukuttan; Phillip A Wilmarth
Journal:  Am J Ophthalmol       Date:  2018-03-17       Impact factor: 5.258

8.  FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression.

Authors:  Leah A Owen; Margaux A Morrison; Jeeyun Ahn; Se Joon Woo; Hajime Sato; Rosann Robinson; Denise J Morgan; Fani Zacharaki; Marina Simeonova; Hironori Uehara; Usha Chakravarthy; Ruth E Hogg; Balamurali K Ambati; Maria Kotoula; Wolfgang Baehr; Neena B Haider; Giuliana Silvestri; Joan W Miller; Evangelia E Tsironi; Lindsay A Farrer; Ivana K Kim; Kyu Hyung Park; Margaret M DeAngelis
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-05-08       Impact factor: 4.799

9.  Misclassification can explain most apparent regression of age-related macular degeneration: results from multistate models with misclassification.

Authors:  Ronald E Gangnon; Kristine E Lee; Barbara E K Klein; Sudha K Iyengar; Theru A Sivakumaran; Ronald Klein
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-03-20       Impact factor: 4.799

Review 10.  Complement activation and choriocapillaris loss in early AMD: implications for pathophysiology and therapy.

Authors:  S Scott Whitmore; Elliott H Sohn; Kathleen R Chirco; Arlene V Drack; Edwin M Stone; Budd A Tucker; Robert F Mullins
Journal:  Prog Retin Eye Res       Date:  2014-12-05       Impact factor: 21.198

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