April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Effect Modifiers of Progression to Advanced AMD Using the Age-Related Eye Disease Study (AREDS) Simple Scale
Author Affiliations & Notes
  • E. Y. Chew
    Epidemiology & Clinical Applications,
    National Eye Inst/NIH, Bethesda, Maryland
  • T. E. Clemons
    Statistics, EMMES Corporation, Rockville, Maryland
  • M. L. Klein
    Ophthalmology, Casey Eye Institute-OHSU, Portland, Oregon
  • E. Agron
    Epidemiology & Clinical Applications,
    National Eye Inst/NIH, Bethesda, Maryland
  • F. L. Ferris, III
    Bldg 10, CRC, Room 3-2531,
    National Eye Inst/NIH, Bethesda, Maryland
  • Age-Related Eye Disease Study Group
    National Eye Inst/NIH, Bethesda, Maryland
  • Footnotes
    Commercial Relationships  E.Y. Chew, None; T.E. Clemons, None; M.L. Klein, None; E. Agron, None; F.L. Ferris, III, None.
  • Footnotes
    Support  NEI Contract for AREDS
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 1625. doi:
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    • Get Citation

      E. Y. Chew, T. E. Clemons, M. L. Klein, E. Agron, F. L. Ferris, III, Age-Related Eye Disease Study Group; Effect Modifiers of Progression to Advanced AMD Using the Age-Related Eye Disease Study (AREDS) Simple Scale. Invest. Ophthalmol. Vis. Sci. 2010;51(13):1625.

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

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Abstract
 
Purpose:
 

To provide 5- and 10-year advanced AMD (AAMD) modified progression rates in AREDS participants using the AREDS simplified clinical scale for participants with drusen ≥ 250 µ and smoking history.

 
Methods:
 

The AREDS simple scale specifies risk categories for a person to develop advanced AMD, defined as neovascular AMD or geographic atrophy that involves the center of the macula. The 5-step scale is based on the presence or absence in each eye of 2 easily identified retinal abnormalities or factors, large drusen (≥ 125µ) and pigment abnormalities. We look at modifications to the 5 and 10 year risks of developing advanced AMD (AAMD) when taking into consideration the presence of giant drusen (≥ 250µ) and/or smoking history.

 
Results:
 

The modified risks are based on 3,619 participants at risk for progression to AAMD both eyes (AMD Category 1, 2 an 3) and 788 participants with AAMD in the fellow eye (AMD Category 4). The estimated 5-year probabilities and 10-year probabilities of AAMD (5-year // 10-year) are shown in the table for participants with giant drusen and by smoking history.  

 
Conclusions:
 

In a predictable way, including the presence of giant drusen ≥ 250µ and/or smoking modifies the in simple scale scores’ risk to progression to AAMD. This can be helpful in discussing risk of progression with patients or identifying risk groups for eligibility in a clinical trial.

 
Clinical Trial:
 

www.clinicaltrials.gov NCT00345176

 
Keywords: age-related macular degeneration 
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