April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
High Serum Concentrations Of Lutein Are Associated With Elevated 8-oxo-dg In Serum Of Normal Subjects
Author Affiliations & Notes
  • John M. Nolan
    Macular Pigment Research Group,
    Waterford Institute of Technology, Waterford, Ireland
  • Lee Coffey
    Pharmaceutical & Molecular Biotechnology Research Centre,
    Waterford Institute of Technology, Waterford, Ireland
  • Kate Loskutova
    Macular Pigment Research Group,
    Waterford Institute of Technology, Waterford, Ireland
  • Jim Stack
    Macular Pigment Research Group,
    Waterford Institute of Technology, Waterford, Ireland
  • James Loughman
    Optometry, Dublin Institute of Technology, Dublin 8, Ireland
  • Stephen Beatty
    Macular Pigment Research Group,
    Waterford Institute of Technology, Waterford, Ireland
  • Footnotes
    Commercial Relationships  John M. Nolan, None; Lee Coffey, None; Kate Loskutova, None; Jim Stack, None; James Loughman, None; Stephen Beatty, None
  • Footnotes
    Support  Fighting Blindness, Ireland
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 3624. doi:
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      John M. Nolan, Lee Coffey, Kate Loskutova, Jim Stack, James Loughman, Stephen Beatty; High Serum Concentrations Of Lutein Are Associated With Elevated 8-oxo-dg In Serum Of Normal Subjects. Invest. Ophthalmol. Vis. Sci. 2011;52(14):3624.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : The aim of this study was to compare 8-hydroxy-2’-deoxyguanosine (8-oxo-dG) levels in serum (a biomarker of oxidative stress) of subjects with high and low serum concentrations of lutein (L).

Methods: : 112 serum samples were selected from a pooled database of normal subjects (n = 485). Subjects with the lowest (n = 56, lowest quartile, Group 1) and highest (n = 56, highest quartile, Group 2) serum concentrations of L (assessed by HPLC) in this database were selected for analysis. We measured a biomarker of oxidative damage in serum using an enzyme-linked immunosorbent assay (ELISA), which measures levels of 8-oxo-dG in serum.

Results: : Mean (± SD) serum concentrations of L were significantly lower in Group 1 when compared to Group 2 (mean [± SD] serum L µmol/L: 0.198 ± 0.036 and 0.883 ± 0.214, respectively, p < 0.01). We report that Group 2 subjects have, on average, significantly higher mean (± SD) 8-oxo-dG levels when compared to Group 1 subjects (8-oxo-dG levels ng/mL: 54.68 ± 18.66 and 40.79 ± 19.59, respectively, p < 0.01).

Conclusions: : The serums with higher serum L concentrations demonstrated higher levels of 8-oxo-dG, indicating (unexpected) higher levels of oxidative stress in these subjects. However, given the known antioxidant properties of L, we suggest that the 8-oxo-dG assay is actually measuring DNA repair (and not oxidative stress), as 8-oxo-dG is released during DNA repair. It is likely that DNA repair enzymes are susceptible to reactive oxygen species and that higher amounts of serum L reduces these species, which gives rise to higher rates of repair. It is also possible that the higher levels of 8-oxo-dG found in the serum represent lower DNA levels of 8-oxo-dG, resulting from the potential antioxidant effect of L.

Keywords: macular pigment • oxidation/oxidative or free radical damage 
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