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Estrogen Receptor Gene Polymorphisms Associated with Incident Aging Macula Disorder

Boekhoorn, S.S. and Vingerling, J.R. and Uitterlinden, A.G. and Meurs, J.B.J. van and Duijn, C.M. van and Pols, H.A.P. and Hofman, A. and Jong de, P.T.V.M. (2007) Estrogen Receptor Gene Polymorphisms Associated with Incident Aging Macula Disorder. Investigative Ophthalmology and Visual Science, 48, 1012-1017. DOI: 10.1167/iovs.06-0577.

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Abstract

PURPOSE. It has been suggested that early menopause increases the risk of aging-macula disorder (AMD), the major cause of incurable blindness with a dry and wet late subtype, and that exposure to endogenous or postmenopausal exogenous estrogens reduces this risk. This study was undertaken to investigate whether genetic variations in the estrogen receptor a(ESR1) gene are associated with incident AMD. METHODS. In the Rotterdam Study, a prospective population-based cohort study of participants aged 55 years and older, associations between ESR1 PvuII-XbaI haplotypes and incident early or late AMD were studied in 4571 participants after a mean follow-up time of 7.7 years. Cox proportional hazards regression was used to estimate hazard ratios (HRs) and corresponding 95% confidence intervals (CIs), with adjustment for the most common confounders. RESULTS. ESR1 PvuII-XbaI haplotype 1 was a risk factor for late AMD. Persons with two copies of haplotype 1 were at 3.20 (95% CI, 1.47¿6.99) times higher risk for late AMD than noncarriers of haplotype 1, after adjustment for age and sex. This increase was more pronounced for wet AMD (hazard ratio [HR] 4.29; 95% CI, 1.47¿12.49) after adjustment for age, sex, smoking, and complement factor H genotype. Correction for additional confounders, including age at menopause, use of hormone replacement therapy, blood pressure, and body mass index did not essentially alter the findings. CONCLUSIONS. Persons with one or two copies of ESR1 PvuII-XbaI haplotype 1 have an increased risk of late AMD, especially of the wet form.

Item Type:Article
Additional Information:DOI: 10.1167/iovs.06-0577
Institutes:Netherlands Institute for Neuroscience (NIN)
ID Code:3787
Deposited On:13 Feb 2009 17:14
Last Modified:10 Dec 2009 13:14

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