Abstract
Aims
To determine the risk of age-related macular degeneration (AMD) progression posed by the presence of each early AMD characteristic.
Methods
A prospective cohort study of 254 participants aged 50 years and older, all with early AMD features at their baseline visit followed for an average of 7 years. Stereoscopic colour fundus photographs were graded for early AMD features using the International Classification System. AMD status was stratified into six exclusive levels along a continuum of disease severity according to drusen type, pigmentary abnormalities, or late AMD. Progression was assessed according to three definitions: a change between or within a severity level, or by side by side grading.
Results
The progression rate of early AMD ranged between 3.4 and 4.67% per annum depending upon the definition used. In total, 15 (6%) cases progressed from early AMD to the late complication of AMD. After controlling for age and smoking, cases with soft indistinct drusen at baseline were at a greater risk of progressing from early to late AMD than were cases without this characteristic (OR=3.72, 95%CI 1.20–11.54; P=0.02).
Conclusion
Our proposed definitions of AMD progression give rates that are consistent with current knowledge of progression and its determinants. Each early AMD characteristic conveys its own risk of progression to an eye, with soft indistinct drusen carrying the greater risk. An international consensus on what defines AMD progression would greatly help the research community when trying to assess the importance of new risk factors and the effectiveness of novel interventions.
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References
VanNewkirk MR, Nanjan MR, Wang JJ, Mitchell P, Taylor HR, McCarty CA . The prevalence of age-related maculopathy: the visual impairment project. Ophthalmology 2000; 107: 1593–1600.
Klaver C, Assink J, van Leeuwen R, Wolfs RC, Vingerling JR, Stijnen T et al. Incidence and progression rates of age-related maculopathy: The Rotterdam Study. Invest Ophthalmol Vis Sci 2001; 42: 2237–2241.
Bressler N, Munoz B, Maguire M, Vitale SE, Schein OD, Taylor HR et al. Five-year incidence and disappearance of drusen and retinal pigment epithelial abnormalities. Waterman Study. Arch Ophthalmol 1995; 113: 301–308.
Klein R, Klein BEK, Jensen S, Meuer S . The five-year incidence and progression of age-related maculopathy: The Beaver Dam Eye Study. Ophthalmology 1997; 104: 7–21.
Sparrow J, Dickinson A, Duke A, Thompson J, Gibson J, Rosenthal A . Seven year follow-up of age-related maculopathy in an elderly British population. Eye 1997; 11: 315–324.
Age-related Eye Disease Study Research Group. A randomized, placebo-controlled, clinical trial of high-dose supplementation with vitamins C and E, beta carotene, and zinc for age-related macular degeneration and vision loss. Arch Ophthalmol 2001; 119: 1417–1436.
van Leeuwen R, Klaver C, Vingerling J, Hofman A, de Jong PTVM . The risk and natural course of age-related maculopathy. Follow-up at 6 1/2 years in the Rotterdam Study. Arch Ophthalmol 2003; 121: 519–526.
Robman L, McNeil JJ, Dimitrov P, Dowrick A, Tikellis G, Nicolas C et al. Methodology of the cardiovascular health and age-related maculopathy (CHARM) Study. Ophthal Epidemiol 2004; 11: 161–179.
Livingston P, Carson C, Stanislavsky Y, Lee S, Guest C, Taylor H . Methods for a population-based study of eye disease: the Melbourne Visual Impairment Project. Ophthalmic Epidemiol 1994; 1: 139–148.
Garrett SKM, McNeil JJ, Silagy C . Methodology of the VECAT Study: vitamin E intervention in cataract and age-related maculopathy. Ophthal Epidemiol 1999; 6: 195–208.
Taylor HR, Tikellis G, Robman LD, McCarty CA, McNeil JJ . Vitamin E supplementation and macular degeneration: randomised controlled trial. BMJ 2002; 325: 7354–7360.
Mc Neil JJ, Robman LD, Tikellis G, Sinclair M, McCarty CA, Taylor HR . Vitamin E supplementation and cataract: randomized controlled trial. Ophthalmology 2004; 111: 75–84.
Bird A, Bressler N, Bressler S, Chisholm IH, Coscas G, Davis MD et al. An international classification and GRADING system for age-related maculopathy and age-related macular degeneration. The International ARM Epidemiological Study Group. Surv Ophthalmol 1995; 39: 333–339.
Tikellis G, Robman LD, Harper CA, Garrett SKM, McNeil JJ, Taylor HR et al. The VECAT Study: methodology and statistical power for measurement of age-related macular features. Ophthal Epidemiol 1999; 6: 181–194.
Robman LD, Tikellis G, Garrett SK, Harper CA, McNeil JJ, Taylor HR et al. Baseline ophthalmic findings in the vitamin E, cataract and age-related maculopathy (VECAT) study. Aust NZ J Ophthalmol 1999; 27: 410–416.
Klein R, Davis M, Magli Y, Segal P, Klein BEK, Hubbard L . The Wisconsin age-related maculopathy grading system. Ophthalmology 1991; 98: 1128–1134.
Mitchell P, Smith W, Attebo K, Wang J . Prevalence of age-related maculopathy in Australia. The Blue Mountains Eye Study. Ophthalmology 1995; 102: 1450–1460.
Bressler SB, Maguire M, Bressler NM, Fine S . Relationship of drusen and abnormalities of the retinal pigment epithelium to the prognosis of neovascular macular degeneration. The Macular Photocoagulation Study Group. Arch Ophthalmol 1990; 108: 1442–1447.
Holz F, Wolfensberger T, Piguet B, Gross-Jendroska M, Wells JA, Minassian DC et al. Bilateral macular drusen in age-related macular degeneration. Prognosis and risk factors. Ophthalmology 1994; 101: 1522–1528.
Klein R, Klein BEK, Tomany S, Meuer SM, Huang GH . Ten-year incidence and progression of age-related maculopathy. The Beaver Dam Eye Study. Ophthalmology 2002; 109: 1767–1779.
Klein R, Klein BEK, Linton K, DeMets D . The Beaver Dam Eye Study: the relation of age-related maculopathy to smoking. Am J Epidemiol 1993; 137: 190–200.
Vingerling J, Hofman A, Grobbee D, de Jong P . Age-related macular degeneration and smoking. The Rotterdam study. Arch Ophthalmol 1996; 114: 1193–1196.
Smith W, Mitchell P, Leeder S . Smoking and age-related maculopathy. The Blue Mountains Eye Study. Arch Ophthalmol 1996; 114: 1518–1523.
Chan D . Cigarette smoking and age-related macular degeneration. Optom Vis Sci 1998; 75: 476–484.
Azad R, Tewari H, Khosla P . Fellow eye in senile disciform degeneration of the macula. Indian J Ophthalmol 1983; 31: 878–881.
Acknowledgements
The CHARM Study is a recipient of a Project Grant from the National Health and Medical Research Council of Australia. Additional support is provided by the Perpetual Trustees Australia Ltd (Ramaciotti Foundation), ANZ Executors & Trustee Company Ltd (The Hugh DT Williamson Foundation under the Medical Research and Technology in Victoria Program), The Royal Victorian Institute for the Blind, The Royal Victorian Eye & Ear Hospital Research Committee, The Lions Club of Victoria, and The Australian Institute of Health and Welfare.
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Tikellis, G., Robman, L., Dimitrov, P. et al. Characteristics of progression of early Age-related macular degeneration: the Cardiovascular Health and Age-related maculopathy Study. Eye 21, 169–176 (2007). https://doi.org/10.1038/sj.eye.6702151
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DOI: https://doi.org/10.1038/sj.eye.6702151
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