April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Quantification and comparison of VEGF-B in the vitreous of patients with diabetic ocular disease and a control group of patients with non-diabetic ocular disease
Author Affiliations & Notes
  • Joana Mesquita
    Biochemistry, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Covilha, Portugal
  • João Paulo Castro Sousa
    Biochemistry, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Covilha, Portugal
    Ophthalmology, Centro Hospitalar de Leiria-Pombal, Leiria, Portugal
  • Ana S Rocha
    Biochemistry, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Covilha, Portugal
  • Fatima Santos
    Biochemistry, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Covilha, Portugal
  • Joao Monteiro
    Biochemistry, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Covilha, Portugal
  • Luís Passarinha
    Biochemistry, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Covilha, Portugal
  • Cândida Tomaz
    Biochemistry, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Covilha, Portugal
  • Footnotes
    Commercial Relationships Joana Mesquita, Novartis (E); João Paulo Castro Sousa, None; Ana Rocha, None; Fatima Santos, None; Joao Monteiro, None; Luís Passarinha, None; Cândida Tomaz, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 399. doi:
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      Joana Mesquita, João Paulo Castro Sousa, Ana S Rocha, Fatima Santos, Joao Monteiro, Luís Passarinha, Cândida Tomaz; Quantification and comparison of VEGF-B in the vitreous of patients with diabetic ocular disease and a control group of patients with non-diabetic ocular disease. Invest. Ophthalmol. Vis. Sci. 2014;55(13):399.

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Abstract
 
Purpose
 

Vascular endothelial growth factor (VEGF) plays a major role in pathological angiogenesis and in retinal diseases. Evidence shows that there are increased levels of VEGF-A in the retina and in the vitreous of patients with retinal diseases, particularly in diabetic patients. Although many studies have been focused in VEGF family, VEGF-B remains poorly studied and its function is the most controversial of the VEGF family. VEGF-B may act as a survival factor under certain conditions or may act as a growth inhibiting factor. However there is a gap to know how VEGF-B is expressed in human eyes and how it is altered in the presence of certain diseases such as diabetes. The aim of the present study was to quantify and compare the VEGF-B in the human vitreous of diabetic and non-diabetic patients with ocular disease.

 
Methods
 

33 samples of human vitreous collected at the beginning of the pars plana vitrectomy from 33 eyes were analyzed and quantified by ELISA assays. Results obtained of quantified VEGF-B (pg/L) were analyzed and compared between a group of diabetic patients with ocular disease (proliferative diabetic retinopathy (PDR)/ epimacular membrane secondary to diabetic maculopathy (ERM)) and a control group of non-diabetic patients with ocular disease (rhegmatogenous retinal detachment). All patients included in this study, which adhered to the tenets of the Declaration of Helsinki, gave their informed consent to surgical treatment.

 
Results
 

The mean VEGF-B concentrations in vitreous were significantly higher in the diabetic patients group (18.82 pg/L ±1.44) vs control group of non-diabetic patients (17.90 pg/L ± 0.32) (p=0.006). No statistically significant difference in the mean vitreous concentrations of VEGF-B was found between the PDR and ERM group (p=0.449).

 
Conclusions
 

The results of the quantification of VEGF-B in vitreous by the used method showed a statistical significant increase in diabetic ocular diseases when compared to non-diabetic ocular diseases. This study shows that VEGF-B may be overexpressed in vitreous of diabetic patients.

  
Keywords: 688 retina • 748 vascular endothelial growth factor • 498 diabetes  
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