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Tytuł:
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Genetic susceptibility, dietary antioxidants, and long-term incidence of age-related macular degeneration in two populations.
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Autorzy:
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Wang JJ; Centre for Vision Research, Department of Ophthalmology and the Westmead Millennium Institute, University of Sydney, Sydney, Australia; Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, Melbourne, Australia. Electronic address: .
Buitendijk GH; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Rochtchina E; Centre for Vision Research, Department of Ophthalmology and the Westmead Millennium Institute, University of Sydney, Sydney, Australia.
Lee KE; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands.
Klein BE; Department of Ophthalmology and Visual Sciences, University of Wisconsin Medical School, Madison, Wisconsin.
van Duijn CM; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Flood VM; Faculty of Health and Behavioural Sciences, University of Wollongong, Wollongong, Australia.
Meuer SM; Department of Ophthalmology and Visual Sciences, University of Wisconsin Medical School, Madison, Wisconsin.
Attia J; Centre for Clinical Epidemiology and Biostatistics, and School of Medicine and Public Health, University of Newcastle, Newcastle, Australia; Department of Medicine, John Hunter Hospital and Hunter Medical Research Institute, Newcastle, Australia.
Myers C; Department of Ophthalmology and Visual Sciences, University of Wisconsin Medical School, Madison, Wisconsin.
Holliday EG; Centre for Clinical Epidemiology and Biostatistics, and School of Medicine and Public Health, University of Newcastle, Newcastle, Australia.
Tan AG; Centre for Vision Research, Department of Ophthalmology and the Westmead Millennium Institute, University of Sydney, Sydney, Australia.
Smith WT; School of Medicine and Public Health, University of Newcastle, Newcastle, Australia; School of Public Health, Sydney Medical School, University of Sydney, Sydney, Australia.
Iyengar SK; Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, Ohio.
de Jong PT; Netherlands Institute of Neurosciences, Institute of the Royal Netherlands Academy of Arts and Sciences, Department of Ophthalmology, AMC, Amsterdam, and Department of Ophthalmology, LUMC, Leiden, The Netherlands.
Hofman A; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands; Netherlands Consortium for Healthy Aging, Netherlands Genomics Initiative, the Hague, The Netherlands.
Vingerling JR; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Mitchell P; Centre for Vision Research, Department of Ophthalmology and the Westmead Millennium Institute, University of Sydney, Sydney, Australia.
Klein R; Department of Ophthalmology and Visual Sciences, University of Wisconsin Medical School, Madison, Wisconsin.
Klaver CC; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
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Źródło:
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Ophthalmology [Ophthalmology] 2014 Mar; Vol. 121 (3), pp. 667-75. Date of Electronic Publication: 2013 Nov 28.
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Typ publikacji:
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Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
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Język:
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English
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Imprint Name(s):
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Publication: 2000- : New York : Elsevier
Original Publication: Rochester, Minn., American Academy of Ophthalmology.
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MeSH Terms:
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Diet*
Genetic Predisposition to Disease*
Antioxidants/*administration & dosage
Macular Degeneration/*epidemiology
Macular Degeneration/*genetics
Aged ; Ascorbic Acid/administration & dosage ; Complement Factor H/genetics ; Fatty Acids, Omega-3/administration & dosage ; Feeding Behavior ; Female ; Fish Products ; Fruit ; Genotyping Techniques ; Humans ; Incidence ; Lutein/administration & dosage ; Macular Degeneration/prevention & control ; Male ; Middle Aged ; Molecular Epidemiology ; Netherlands/epidemiology ; New South Wales/epidemiology ; Proteins/genetics ; Surveys and Questionnaires ; Vegetables ; Xanthophylls/administration & dosage ; Zeaxanthins ; Zinc Compounds/administration & dosage ; beta Carotene/administration & dosage
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Substance Nomenclature:
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0 (ARMS2 protein, human)
0 (Antioxidants)
0 (CFH protein, human)
0 (Fatty Acids, Omega-3)
0 (Proteins)
0 (Xanthophylls)
0 (Zeaxanthins)
0 (Zinc Compounds)
01YAE03M7J (beta Carotene)
80295-65-4 (Complement Factor H)
PQ6CK8PD0R (Ascorbic Acid)
X72A60C9MT (Lutein)
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Entry Date(s):
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Date Created: 20131203 Date Completed: 20140506 Latest Revision: 20210514
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Update Code:
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20240104
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DOI:
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10.1016/j.ophtha.2013.10.017
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PMID:
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24290803
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Objective: To examine effect modification between genetic susceptibility to age-related macular degeneration (AMD) and dietary antioxidant or fish consumption on AMD risk.
Design: Pooled data analysis of population-based cohorts.
Participants: Participants from the Blue Mountains Eye Study (BMES) and Rotterdam Study (RS).
Methods: Dietary intakes of antioxidants (lutein/zeaxanthin [LZ], β-carotene, and vitamin C), long-chain omega-3 polyunsaturated fatty acids, and zinc were estimated from food frequency questionnaires. The AMD genetic risk was classified according to the number of risk alleles of CFH (rs1061170) or ARMS2 (rs10490924) as low (no or 1 risk allele) or high (≥ 2 risk alleles). Interactions between dietary intake and genetic risk levels were assessed. Associations between dietary intake and AMD risk were assessed comparing the highest with the 2 lower intake tertiles by genetic risk subgroups using discrete logistic regression, conducted in each study separately and then using pooled data. Participants without AMD lesions at any visit were controls. We adjusted for age and sex in analyses of each cohort sample and for smoking status and study site in pooled-data analyses.
Main Outcome Measures: All 15-year incident late AMD cases were confirmed by chief investigators of the Beaver Dam Eye Study, BMES, and RS. Intergrader reproducibility was assessed in an early AMD subsample, with 86.4% agreement between BMES and RS graders, allowing for a 1-step difference on a 5-step AMD severity scale.
Results: In pooled data analyses, we found significant interaction between AMD genetic risk status and LZ intake (P=0.0009) but nonsignificant interactions between genetic risk status and weekly fish consumption (P=0.05) for risk of any AMD. Among participants with high genetic risk, the highest intake tertile of LZ was associated with a >20% reduced risk of early AMD, and weekly consumption of fish was associated with a 40% reduced risk of late AMD. No similar association was evident among participants with low genetic risk. No interaction was detected between β-carotene or vitamin C and genetic risk status.
Conclusions: Protection against AMD from greater LZ and fish consumption in persons with high genetic risk based on 2 major AMD genes raises the possibility of personalized preventive interventions.
(Copyright © 2014 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.)
