May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Association of Calcified Drusen With Progression of AMD in AREDS Participants
Author Affiliations & Notes
  • J.R. Armstrong
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • L.D. Hubbard
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • M.D. Davis
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • R.P. Danis
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • L.–Y. Lee
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • B. Zhang
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • R. Klein
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • B.E. Klein
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • AREDS Research Group
    Ophthalmology & Visual Sciences, University of Wisconsin – Madison, Madison, WI
  • Footnotes
    Commercial Relationships  J.R. Armstrong, None; L.D. Hubbard, None; M.D. Davis, None; R.P. Danis, None; L. Lee, None; B. Zhang, None; R. Klein, None; B.E. Klein, None.
  • Footnotes
    Support  NIH Grant EYE02130
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 2128. doi:
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      J.R. Armstrong, L.D. Hubbard, M.D. Davis, R.P. Danis, L.–Y. Lee, B. Zhang, R. Klein, B.E. Klein, AREDS Research Group; Association of Calcified Drusen With Progression of AMD in AREDS Participants . Invest. Ophthalmol. Vis. Sci. 2006;47(13):2128.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To assess the association of calcified drusen with progression of AMD, and to illustrate the course of such eyes, in the Age–Related Eye Disease Study (AREDS).

Methods: : Calcified drusen are small refractile deposits associated with AMD, particularly geographic atrophy (GA). We compared 5–year rates of progression to advanced AMD (neovascular AMD and/or central GA), and to the development of noncentral GA, in eyes with and without calcified drusen. We limited the analysis to eyes that at baseline (a) were in AREDS category 3 (having at least one large ordinary druse [>= 125µm] or extensive intermediate drusen), (b) did not already have non–central GA, and (c) had 5 years of follow–up. We used the extended AREDS severity scale to concentrate this analysis on eyes in levels 6–8, defined as having extensive drusen area and/or pigment abnormalities but without GA. Because both eyes of one subject could have calcified drusen, we present our results based upon only right eyes.

Results: : Among 1086 right eyes in AREDS category 3, 75 eyes (4%) had calcified drusen and 2069 eyes (96%) did not. Progression rates to advanced AMD were 39% vs.13% respectively (p<0.0001 by chi–square). Dividing these progressions, neovascular AMD rates were 13% vs. 8%, central GA rates were 26% vs. 5%, and neoAMD with GA rates were none vs. 1%, respectively. Non–central GA incidence rates were 37% vs. 8%, respectively. Restricted to the 555 right eyes in AREDS levels 6–8, 38 eyes (7%) had calcified drusen and 517 eyes (93%) did not, with progression rates to advanced AMD of 39% and 25%, respectively, (p < 0.0001). Neovascular AMD rates were 13% vs. 14%, central GA rates were 26% vs. 9%, and neoAMD with GA rates were none vs. 2%, respectively. Non–central GA incidence rates were 37% vs. 13%, respectively. Considering the left eye of these 38 subjects with calcified drusen in their right eye, 36 (95%) also had this finding in their contralateral eye. Conducting the outcome analysis for left eyes yielded results very similar to those for right eyes.

Conclusions: : AREDS results show that presence of calcified drusen at baseline signifies 3– to 4–fold increased risk for 5–year progression to geographic atrophy, both central and non–central.

Keywords: age-related macular degeneration • drusen • clinical (human) or epidemiologic studies: risk factor assessment 
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