April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Correlation of Long-chain Polyunsaturated Fatty Acids (LC-PUFAs) in Serum, RBC and Fat with Very-long-chain Polyunsaturated Fatty Acids (VLC-PUFAs) in Human Retina
Author Affiliations & Notes
  • Aruna Gorusupudi
    Deparment of Ophthalmology and Visual Sciences, Moran Eye Center, Salt Lake City, UT
  • Aihua Liu
    Deparment of Ophthalmology and Visual Sciences, Moran Eye Center, Salt Lake City, UT
  • Paul S Bernstein
    Deparment of Ophthalmology and Visual Sciences, Moran Eye Center, Salt Lake City, UT
  • Footnotes
    Commercial Relationships Aruna Gorusupudi, None; Aihua Liu, None; Paul Bernstein, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 624. doi:
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      Aruna Gorusupudi, Aihua Liu, Paul S Bernstein; Correlation of Long-chain Polyunsaturated Fatty Acids (LC-PUFAs) in Serum, RBC and Fat with Very-long-chain Polyunsaturated Fatty Acids (VLC-PUFAs) in Human Retina. Invest. Ophthalmol. Vis. Sci. 2014;55(13):624.

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

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Abstract

Purpose: Recent studies on VLC-PUFAs (C24-36) have revealed their specific presence and importance in retina. Mouse model and human clinical studies indicate that deficiency of VLC-PUFAs in the retina may be a factor in macular pathology and dysfunction in inherited retinal disease and AMD. Unlike LC-PUFAs such as DHA, AA and EPA, VLC-PUFAs are not present in normal human diet, but must be synthesized in vivo from LC-PUFAs. The n3/n6 LC-PUFA ratios, biomarkers of oxidative stress, could therefore influence these ratios in VLC PUFAs of the human retina. In this study, we examined whether levels and n3/n6 ratios of LC-PUFAs in serum, RBC and orbital fat reflect the levels and n3/n6 ratios of VLC-PUFAs in human retina.

Methods: Human donor eyes were collected from the Utah Lions Eye Bank, and 4 mm peripheral retinal punches were used for VLC PUFA analysis. Fatty acid methyl esters were extracted using a standardized method and analyzed by GC-MS (electron ionization mode). Two methods (A and B) were adopted, method A was used to analyze the LC-PUFAs while method B was used to analyze C24- C36 VLC-PUFAs.

Results: The n3/n6 LC-PUFA ratios in serum and RBC positively correlate with the n3/n6 ratios of VLC-PUFAs in human retina. EPA/AA ratios in serum, RBC and orbital fat positively correlate (r=0.92, 0.95 and 0.72) with the VLC-PUFA levels in retina, where as DHA/AA ratios do not correlate. The n3 precursors (18:3, 20:5, 22:5) and n6 precursors (20:4) in RBC are positively associated with retinal n3 and n6 VLC-PUFA levels, respectively.

Conclusions: EPA and AA, but not DHA act as plausible precursors for synthesis of retinal VLC-PUFAs, and LC-PUFAs in serum and RBC can serve as biomarkers to predict the levels and n3/n6 ratios of VLC-PUFAs in human retina. These findings indicate that diet plays an important role in determining levels and composition of VLC-PUFAs in the human retina.

Keywords: 583 lipids • 592 metabolism • 618 nutritional factors  
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