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. Author manuscript; available in PMC: 2006 May 17.
Published in final edited form as: Arch Ophthalmol. 2001 Oct;119(10):1417–1436. doi: 10.1001/archopht.119.10.1417

Table 4.

Effect of Treatment on Risk of Progression to Advanced AMD*

Participants in AMD Categories 2, 3, and 4 (n = 3609)
Participants in AMD Categories 3 and 4 (n = 2556)
Treatment OR (99% CI) PValue OR (99% CI) PValue
Antioxidants vs no antioxidants 0.87 (0.70–1.09) .12 0.83 (0.66–1.06) .05
Zinc vs no zinc 0.82 (0.66–1.03) .02 0.79 (0.62–0.99) .009
Antioxidants vs placebo 0.80 (0.59–1.09) .07 0.76 (0.55–1.05) .03
Adjusted 0.77 (0.56–1.05) .03 0.76 (0.54–1.05) .03
Zinc vs placebo 0.75 (0.55–1.03) .02 0.71 (0.52–0.99) .008
Adjusted 0.71 (0.51–0.98) .005 0.70 (0.50–0.97) .005
Antioxidants + zinc vs placebo 0.72 (0.52–0.98) .007 0.66 (0.47–0.91) .001
Adjusted 0.68 (0.49–0.93) .002 0.66 (0.47–0.93) .001
Total No. of participants with events 803 775
*

Advanced age-related macular degeneration (AMD) indicates photocoagulation or other treatment for choroidal neovascularization, central geographic atrophy, nondrusenoid retinal pigment epithelial detachment, serous or hemorrhagic retinal detachment, hemorrhage under the retina or pigment epithelium, or subretinal fibrosis; OR, odds ratio; and CI, confidence interval. Analysis by repeated-measures logistic regression, unadjusted. P≤.01 is considered statistically significant.

Adjusted for age, sex, race, AMD category, and baseline smoking status.