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Long-term effects of vitamins C and E, β-carotene, and zinc on age-related macular degeneration: AREDS report no. 35
Journal article   Peer reviewed

Long-term effects of vitamins C and E, β-carotene, and zinc on age-related macular degeneration: AREDS report no. 35

Emily Y Chew, Traci E Clemons, Elvira Agrón, Robert D Sperduto, John Paul Sangiovanni, Natalie Kurinij, Matthew D Davis and Age-Related Eye Disease Study Research Group
Ophthalmology (Rochester, Minn.), Vol.120(8), pp.1604-e4
08/2013
DOI: 10.1016/j.ophtha.2013.01.021
PMCID: PMC3728272
PMID: 23582353
url
https://www.ncbi.nlm.nih.gov/pmc/articles/3728272View
Open Access

Abstract

To describe the long-term effects (10 years) of the Age-Related Eye Disease Study (AREDS) formulation of high-dose antioxidants and zinc supplement on progression of age-related macular degeneration (AMD). Multicenter, randomized, controlled, clinical trial followed by an epidemiologic follow-up study. We enrolled 4757 participants with varying severity of AMD in the clinical trial; 3549 surviving participants consented to the follow-up study. Participants were randomly assigned to antioxidants C, E, and β-carotene and/or zinc versus placebo during the clinical trial. For participants with intermediate or advanced AMD in 1 eye, the AREDS formulation delayed the progression to advanced AMD. Participants were then enrolled in a follow-up study. Eye examinations were conducted with annual fundus photographs and best-corrected visual acuity assessments. Medical histories and mortality were obtained for safety monitoring. Repeated measures logistic regression was used in the primary analyses. Photographic assessment of progression to, or history of treatment for, advanced AMD (neovascular [NV] or central geographic atrophy [CGA]), and moderate visual acuity loss from baseline (≥15 letters). Comparison of the participants originally assigned to placebo in AREDS categories 3 and 4 at baseline with those originally assigned to AREDS formulation at 10 years demonstrated a significant (P<0.001) odds reduction in the risk of developing advanced AMD or the development of NV AMD (odds ratio [OR], 0.66, 95% confidence interval [CI], 0.53-0.83 and OR, 0.60; 95% CI, 0.47-0. 78, respectively). No significant reduction (P = 0.93) was seen for the CGA (OR, 1.02; 95% CI, 0.71-1.45). A significant reduction (P = 0.002) for the development of moderate vision loss was seen (OR 0.71; 95% CI, 0.57-0.88). No adverse effects were associated with the AREDS formulation. Mortality was reduced in participants assigned to zinc, especially death from circulatory diseases. Five years after the clinical trial ended, the beneficial effects of the AREDS formulation persisted for development of NV AMD but not for CGA. These results are consistent with the original recommendations that persons with intermediate or advanced AMD in 1 eye should consider taking the AREDS formulation. The authors have no proprietary or commercial interest in any of the materials discussed in this article.
Photography Epidemiologic Studies Zinc Oxide - therapeutic use beta Carotene - therapeutic use Follow-Up Studies Humans Middle Aged Male Survival Rate Vitamins - therapeutic use Macular Degeneration - diagnosis Macular Degeneration - drug therapy Antioxidants - therapeutic use Macular Degeneration - mortality Ascorbic Acid - therapeutic use Vitamin E - therapeutic use Aged, 80 and over Female Aged Drug Therapy, Combination Odds Ratio Visual Acuity - physiology

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