4.5 Article

Candidate gene study of macular response to supplemental lutein and zeaxanthin

Journal

EXPERIMENTAL EYE RESEARCH
Volume 115, Issue -, Pages 172-177

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exer.2013.07.020

Keywords

macular pigment; lutein; genetics; supplementation; macular degeneration

Categories

Funding

  1. Wellcome Trust
  2. European Union MyEuropia Marie Curie Research Training Network
  3. Guide Dogs for the Blind Association
  4. European Community [HEALTHF-22008201865GEFOS]
  5. ENGAGE [HEALTHF42007201413]
  6. FP-5 GenomEUtwin Project [QLG2CT200201254]
  7. US National Institutes of Health/National Eye Institute [1RO1EY018246]
  8. NIH Center for Inherited Disease Research
  9. National Institute for Health Research (NIHR) Clinical Research Facility at Guy's & St Thomas' NHS Foundation Trust
  10. NIHR Biomedical Research Centre based at Guy's and St Thomas' NHS Foundation Trust
  11. King's College London
  12. Fight for Sight
  13. Worshipful Company of Spectacle Makers
  14. TFC Frost Fellowship
  15. Fight for Sight [1329/30] Funding Source: researchfish
  16. Medical Research Council [MR/K023721/1] Funding Source: researchfish
  17. National Institute for Health Research [SRF/01/010] Funding Source: researchfish
  18. MRC [MR/K023721/1] Funding Source: UKRI

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Supplementation with carotenoids is proposed to protect against age-related macular degeneration. There is, however, considerable variability in retinal macular pigment response, which may be due to underlying genetic variation. The purpose of this study was to determine whether genetic factors, which have been previously associated with cross-sectional macular pigment levels in the retina or serum lutein, also influence response to supplementation. To this end we conducted an association study in 310 subjects from the TwinsUK cohort between variants in 8 candidate genes and serum lutein and retinal macular pigment optical density (MPOD) levels before and after supplementation. Four variants were associated with MPOD response to supplementation (p < 0.05): rs11057841 (SCARB1), rs4926339 (RPE65), rs1929841 (ABCA1) and rs174534 (FADS)). We also confirmed previous associations between rs6564851 near BMCO1 (p < 0.001) and rs11057841 within SCARB1 (p = 0.01) and baseline measures of serum lutein; while the latter was also associated with MPOD response, none of the BMCO1 variants were. Finally, there was evidence for association between variants near RPE65 and ELOVL2 and changes in lutein concentration after supplementation. This study is the first to show association between genetic variants and response to carotenoids supplementation. Our findings suggest an important link between MP response and the biological processes of carotenoids transport and fatty acid metabolism. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.

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