December 2002
Volume 43, Issue 13
Free
ARVO Annual Meeting Abstract  |   December 2002
Soluble Fas Ligand In Human Plasma: An Increase With Aging And Age-related Macular Degeneration
Author Affiliations & Notes
  • S Jiang
    Ophthalmology
    Emory University Atlanta GA
  • SE Moriarty
    Ophthalmology
    Emory University Atlanta GA
  • J Shah
    Ophthalmology
    Emory University Atlanta GA
  • DP Jones
    Biochemistry
    Emory University Atlanta GA
  • P Sternberg
    Ophthalmology
    Emory University Atlanta GA
  • Footnotes
    Commercial Relationships   S. Jiang, None; S.E. Moriarty, None; J. Shah, None; D.P. Jones, None; P. Sternberg, None. Grant Identification: NIH grants EY07892, EY06360, ES09047, AFAR, NRSA,
Investigative Ophthalmology & Visual Science December 2002, Vol.43, 2819. doi:
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    • Get Citation

      S Jiang, SE Moriarty, J Shah, DP Jones, P Sternberg; Soluble Fas Ligand In Human Plasma: An Increase With Aging And Age-related Macular Degeneration . Invest. Ophthalmol. Vis. Sci. 2002;43(13):2819.

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

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Abstract

Abstract: : Purpose: Fas ligand (FasL), a member of the tumor necrosis factor family, induces apoptosis in Fas-bearing cells. Its soluble form, sFasL, is found to increase in many diseases. The purpose of this study was to determine whether there was a change of sFasL in the human plasma with aging and appearance of age-related macular degeneration (ARMD). Methods: Blood samples were collected from 139 non-ARMD and 15 ARMD subjects ranging in age from 44 to 85. Patients carrying the diagnosis of ARMD had a minimal of 5 drusen in at least one eye; with some vision loss related the disease. Plasma soluble FasL was determined by sandwich sFasL kit. Results: A variable level of sFasL was detected in human plasma. The concentration of sFasL in the plasma was increased with aging. The plasma sFasL level was significant higher in age ≷ 60 group than age < 60 group. However, no difference in the plasma sFasL was seen between female and male subjects. The sFasL in the plasma from ARMD was 2 times higher than in age-matched non-ARMD controls, but was not statistically significant with the small number of ARMD subjects (p = 0.108). Conclusions: sFasL increases in relation to the age and possibly with ARMD. These results suggest that sFasL may play a role in the pathogenesis of ARMD. CR: None. Support: NIH grants EY07892, EY06360, ES09047, RPB, NRSA, FFB, and AFAR.

Keywords: 308 age-related macular degeneration • 309 aging • 341 cell death/apoptosis 
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