Brief Communication abstract


Nature Genetics 40, 1160 - 1162 (2008)
Published online: 7 September 2008 | doi:10.1038/ng.210

Common variants of FUT2 are associated with plasma vitamin B12 levels

Aditi Hazra1,2, Peter Kraft1, Jacob Selhub3, Edward L Giovannucci2,4, Gilles Thomas5, Robert N Hoover5, Stephen J Chanock5 & David J Hunter1,2,4,5,6

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We identified a strong association (P = 5.36 times 10-17) between rs492602 in FUT2 and plasma vitamin B12 levels in a genome-wide scan (n = 1,658) and an independent replication sample (n = 1,059) from the Nurses' Health Study. Women homozygous for the rs492602[G] allele had higher B12 levels. This allele is in strong linkage disequilibrium with the FUT2 nonsecretor variant encoding W143X, suggesting a plausible mechanism for altered B12 absorption and plasma levels.

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  1. Program in Molecular and Genetic Epidemiology, Department of Epidemiology, Harvard School of Public Health, 677 Huntington Avenue, Boston, Massachusetts 02115, USA.
  2. Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, 181 Longwood Avenue, Boston, Massachusetts 02115, USA.
  3. Vitamin Metabolism and Aging Laboratory, Jean Mayer US Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts 02111, USA.
  4. Department of Nutrition, Harvard School of Public Health, 677 Huntington Avenue, Boston, Massachusetts 02115, USA.
  5. Division of Cancer Epidemiology and Genetics, National Cancer Institute(NCI), US National Institutes of Health (NIH), Department of Health and Human Services (DHHS), Bethesda, Maryland 20892, USA.
  6. Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.

Correspondence to: David J Hunter1,2,4,5,6 e-mail: dhunter@hsph.harvard.edu



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