Associations between Aspirin Use and Aging Macula Disorder:
The European Eye Study
Objective
To study associations between aspirin use and early and late aging macula disorder (AMD).
Design
Population-based cross-sectional European Eye Study in 7 centers from northern to southern Europe.
Participants
In total, 4691 participants 65 years of age and older, collected by random sampling.
Methods
Aspirin intake and possible confounders for AMD were ascertained by a structured questionnaire. Ophthalmic and basic systemic measurements were performed in a standardized way. The study classified AMD according to the modified International Classification System on digitized fundus images at 1 grading center. Nonfasting blood samples were analyzed in a single laboratory. Associations were analyzed by logistic regression.
Main Outcome Measures
Odds ratios (ORs) for AMD in aspirin users.
Results
Early AMD was present in 36.4% of the participants and late AMD was present in 3.3% of participants. Monthly aspirin use was reported by 1931 (41.2%), at least once weekly by 7%, and daily use by 17.3%. For daily aspirin users, the ORs, adjusted for potential confounders, showed a steady increase with increasing severity of AMD grades. These were: grade 1, 1.26 (95% confidence interval [CI], 1.08–1.46; P<0.001); grade 2, 1.42 (95% CI, 1.18–1.70), and wet late AMD, 2.22 (95% CI, 1.61–3.05).
Conclusions
Frequent aspirin use was associated with early AMD and wet late AMD, and the ORs rose with increasing frequency of consumption. This interesting observation warrants further evaluation of the associations between aspirin use and AMD.
Financial Disclosure(s)
The author(s) have no proprietary or commercial interest in any materials discussed in this article.
Manuscript no. 2010-1537.
Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.
The European Eye Study was supported by the European Commission Vth Framework (QLK6-CT-1999–02094), Brussels, Belgium. Additional funding for cameras was provided by the Macular Disease Society UK, Andover, UK. Dr. Rahu was financed by the Estonian Ministry of Education and Science (target funding 01921112s02 and SF0940026s07), Tartu, Estonia. Additional funding in Alicante was received from the Spanish Ministry of Health (grant nos.: FIS 01/1692E and RCESP C 03/09), Madrid, Spain, CIBER de Epidemiologiá y Salud Pública, and the Generalitat Valenciana (grant nos.: CTGCA/2002/06 and G03/136), Valencia, Spain. The sponsors or funding organizations had no role in study design, data collection, data analysis, data interpretation, writing of the paper, or decision to submit the paper for publication.
PII: S0161-6420(11)00568-9
doi:10.1016/j.ophtha.2011.06.025
© 2012 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

