4.7 Article

Common Variation in the β-Carotene 15,15′-Monooxygenase 1 Gene Affects Circulating Levels of Carotenoids: A Genome-wide Association Study

Journal

AMERICAN JOURNAL OF HUMAN GENETICS
Volume 84, Issue 2, Pages 123-133

Publisher

CELL PRESS
DOI: 10.1016/j.ajhg.2008.12.019

Keywords

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Funding

  1. Italian Ministry of Health [ICS110.1\RS97.71]
  2. National Institute on Aging [N01-AG-916413, N01-AG-821336]
  3. US Public Health Service [N01-CN-45165, N01-RC-45035, N01-RC-37004]
  4. National Cancer Institute, Department of Health and Human Service
  5. National Institute on Aging, National Institutes of Health
  6. National Institute on Aging, Pathogenesis of Physical Disability in Aging Women [R37 AG 19905, R01 AG027012]
  7. Johns Hopkins Claude D. Pepper Older Americans Independence Center [P30 AG021334]

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Low plasma levels of carotenoids and tocopherols are associated with increased risk of chronic disease and disability. Because dietary intake of these lipid-soluble antioxidant vitamins is only poorly correlated with plasma levels, we hypothesized that circulating carotenoids (vitamin A-related compounds) and tocopherols (vitamin E-related compounds) are affected by common genetic variation. By conducting a genome-wide association Study in a sample of Italians (n = 1190), we identified novel common variants associated with circulating carotenoid levels anti known lipid variants associated with alpha-tocopherol levels. Effects were replicated in the Women's Health and Aging Study (n = 615) and in the alpha-Tocopherol, beta-Carotene Cancer Prevention (ATBC) study (n 2136). In meta-analyses including all three Studies, the G allele at rs6564851, near the beta-carotene 15,15'-monooxygenase 1 (BCMO1) gene, was associated with higher beta-carotene (p = 1.6 x 10(-24)) and alpha-carotene (p = 0.0001) levels and lower lycopene (0.003), zeaxanthin (p = 1.3 x 10(-5)), and lutein (p = 7.3 x 10(-15)) levels, with effect sizes ranging from 0.10-0.28 SDs per allele. Interestingly, this genetic variant had no significant effect on plasma retinol (p > 0.05). The SNP rs12272004, in linkage disequilibrium with the S19W variant in the APOA5 gene, was associated with alpha-tocopherol (meta-analysis p = 7.8 x 10(-10)) levels, and this association was substantially weaker when we adjusted for triglyceride levels (p = 0.002). Our findings might shed light on the controversial relationship between lipid-soluble anti-oxidant nutrients and human health.

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