Incidence, progression and risk factors of age-related macular degeneration in 35–95-year-old individuals from three jointly designed German cohort studies

Author:

Brandl CarolineORCID,Günther Felix,Zimmermann Martina EORCID,Hartmann Kathrin I,Eberlein Gregor,Barth Teresa,Winkler Thomas W,Linkohr Birgit,Heier Margit,Peters Annette,Li Jeany QORCID,Finger Robert P,Helbig Horst,Weber Bernhard H F,Küchenhoff Helmut,Mueller Arthur,Stark Klaus J,Heid Iris M

Abstract

ObjectiveTo estimate age-related macular degeneration (AMD) incidence/progression across a wide age range.Methods and analysisAMD at baseline and follow-up (colour fundus imaging, Three Continent AMD Consortium Severity Scale, 3CACSS, clinical classification, CC) was assessed for 1513 individuals aged 35–95 years at baseline from three jointly designed population-based cohorts in Germany:Kooperative Gesundheitsforschung in derRegionAugsburg (KORA-Fit, KORA-FF4) andAltersbezogeneUntersuchungen zurGesundheit derUniversitätRegensburg (AugUR) with 18-year, 14-year or 3-year follow-up, respectively. Baseline assessment included lifestyle, metabolic and genetic markers. We derived cumulative estimates, rates and risk factor association for: (1) incident early AMD, (2) incident late AMD among no AMD at baseline (definition 1), (3) incident late AMD among no/early AMD at baseline (definition 2), (4) progression from early to late AMD.ResultsIncidence/progression increased by age, except progression in 70+-year old. We observed 35–55-year-old with 3CACSS-based early AMD who progressed to late AMD. Predominant risk factor for incident late AMD definition 2 was early AMD followed by genetics and smoking. When separating incident late AMD definition 1 from progression (instead of combined as incident late AMD definition 2), estimates help judge an individual’s risk based on age and (3CACSS) early AMD status: for example, for a 65-year old, 3-year late AMD risk with no or early AMD is 0.5% or 7%, 3-year early AMD risk is 3%; for an 85-year old, these numbers are 0.5%, 21%, 12%, respectively. For CC-based ‘early/intermediate’ AMD, incidence was higher, but progression was lower.ConclusionWe provide a practical guide for AMD risk for ophthalmology practice and healthcare management and document a late AMD risk for individuals aged <55 years.

Funder

Institute of Human Genetics, University of Regensburg

German Research Foundation

Helmholtz Zentrum München - German Research Center for Environmental Health

Department of Genetic Epidemiology, University of Regensburg

German Federal Ministry of Education and Research

National Institutes of Health

PRO RETINA Foundation

Publisher

BMJ

Subject

Ophthalmology

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