4.7 Article

Polymorphisms in the CD36/FAT gene are associated with plasma vitamin E concentrations in humans

Journal

AMERICAN JOURNAL OF CLINICAL NUTRITION
Volume 93, Issue 3, Pages 644-651

Publisher

OXFORD UNIV PRESS
DOI: 10.3945/ajcn.110.004176

Keywords

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Funding

  1. Direction Generale de la Sante (Ministry of Health)
  2. Mederic
  3. Ipsen
  4. Mutuelle Generale de l'Education Nationale
  5. SODEXHO
  6. Pierre Fabre
  7. Agence Nationale de la Recherche [ANR-05-PNRA-010]
  8. European Union [FOOD-CT-2005-007034]
  9. Universidad Politecnica de Madrid [CH/018/2008]
  10. Axis-Shield Diagnostics Ltd (Oslo, Norway)
  11. Abbot Cientifica SA (Spain)
  12. Spanish Ministry of Education [EX-2007-1124]
  13. Cognis GmbH (Germany)

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Background: Blood vitamin E concentrations are modulated by dietary, metabolic, and genetic factors. CD36 (cluster of differentiation 36), a class B scavenger receptor, might be involved in tissue vitamin E uptake and thus would influence blood vitamin E concentrations. Objective: The goal of the study was to assess the association between CD36 single nucleotide polymorphisms (SNPs) and plasma alpha-tocopherol concentrations in humans. Design: A subsample from the adult SU.VI.MAX (SUpplementation en VItamines et Mineraux AntioXydants) cohort (n = 621) and the adolescent cross-sectional HELENA (Healthy Lifestyle in Europe by Nutrition in Adolescence) Study (n = 993) were genotyped for CD36 SNPs (4 and 10 SNPs, respectively). Fasting plasma alpha-tocopherol concentrations were assayed by using HPLC. Associations were determined by haplotype analyses and by general linear regression models. Results: In the SU.VI.MAX subsample, haplotype analyses showed that some haplotypes of SNPs rs1984112, rs1527479, rs7755, and rs1527483 tended to be associated with plasma alpha-tocopherol concentrations (P = 0.08 and P = 0.09 for haplotypes 1222 and 1122, respectively). We then investigated the whole known common genetic variability (10 SNPs) of CD36 in the HELENA Study. Three SNPs were associated with lower plasma a-tocopherol concentrations (rs1984112: -3.2%, P = 0.053; rs1761667: -2.9%, P = 0.046; rs1527479: -3.7%, P = 0.0061). After correction for multiple testing, the association between rs1527479 and alpha-tocopherol concentrations remained significant. This association was modulated by concentrations of fasting serum triglycerides (P for interaction = 0.006) and long-chain polyunsaturated fatty acids (P for interaction = 0.005). Conclusion: Our results suggest that CD36 can modulate blood alpha-tocopherol concentrations and may therefore be involved in the intestinal absorption or tissue uptake of vitamin E. Am J Clin Nutr 2011;93:644-51.

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