The reduction of serum soluble Flt-1 in patients with neovascular age-related macular degeneration

Am J Ophthalmol. 2015 Jan;159(1):92-100.e1-2. doi: 10.1016/j.ajo.2014.09.036. Epub 2014 Oct 18.

Abstract

Purpose: To evaluate serum soluble Flt-1 (sFlt-1) in age-related macular degeneration (AMD) patients.

Design: Case-control study.

Methods: Study involved 56 non-AMD participants, 53 early AMD patients, and 97 neovascular AMD patients from Belfast in Northern Ireland. Serum samples were collected from each patient. Serum sFlt-1 was measured by human sVEGFR1/sFlt-1 ELISA kit. The results were analyzed by Excel and SPSS.

Results: Serum sFlt-1 concentration of non-AMD, early AMD, and neovascular AMD were 90.8 ± 2.9 pg/mL (± standard error of the mean), 88.2 ± 2.6 pg/mL, and 79.9 ± 2.2 pg/mL. sFlt-1 from neovascular AMD patients was significantly decreased compared to non-AMD and early AMD patients (ANOVA, P < .01). For each 10-point increase in sFlt-1, the odds for having neovascular AMD compared with non-AMD and neovascular AMD decrease by 27.8%, odds ratio (OR) = 0.722 (95% confidence interval [CI]: 0.588-0.888, P = .002) and 27.0%, OR = 0.730 (95% CI: 0.594-0.898, P = .003), respectively. In patients over 73 years of age, serum sFlt-1 <80 pg/mL was associated with a >6-fold higher risk of neovascular AMD.

Conclusions: Reduced serum sFlt-1 differentiates those patients with neovascular AMD from both early AMD and non-AMD participants. In those aged over 73, serum sFlt <80 pg/mL seems to indicate a particularly high risk of neovascular AMD. Our results indicate serum sFlt-1 could be a biomarker for development of neovascular AMD.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Analysis of Variance
  • Biomarkers / blood
  • Case-Control Studies
  • Choroidal Neovascularization / blood*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Humans
  • Macular Degeneration / blood*
  • Male
  • Middle Aged
  • Odds Ratio
  • Risk Factors
  • Vascular Endothelial Growth Factor Receptor-1 / blood*

Substances

  • Biomarkers
  • FLT1 protein, human
  • Vascular Endothelial Growth Factor Receptor-1