June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Quantitative Analysis of Vitreous Humor Reveals Distinct Protein Profiles in Patients with Retinopathy of Prematurity
Author Affiliations & Notes
  • sonika rathi
    Kallam Anji Reddy Molecular Genetics Laboratory, L.V.Prasad Eye Institute, Hyderabad, India
  • Subhabrata Chakrabarti
    Kallam Anji Reddy Molecular Genetics Laboratory, L.V.Prasad Eye Institute, Hyderabad, India
  • Ganeswara Musada
    Kallam Anji Reddy Molecular Genetics Laboratory, L.V.Prasad Eye Institute, Hyderabad, India
  • Subhadra Jalali
    Smt. Kannuri Santhamma Centre for Vitreo Retinal Diseases, L.V.Prasad Eye Institute, Hyderabad, India
  • Ramesh Kekunnaya
    Jasti V Ramanamma Children’s Eye Care Centre, L.V.Prasad Eye Institute, Hyderabad, India
  • Inderjeet Kaur
    Kallam Anji Reddy Molecular Genetics Laboratory, L.V.Prasad Eye Institute, Hyderabad, India
  • Footnotes
    Commercial Relationships sonika rathi, None; Subhabrata Chakrabarti, None; Ganeswara Musada, None; Subhadra Jalali, None; Ramesh Kekunnaya, None; Inderjeet Kaur, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 587. doi:
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      sonika rathi, Subhabrata Chakrabarti, Ganeswara Musada, Subhadra Jalali, Ramesh Kekunnaya, Inderjeet Kaur; Quantitative Analysis of Vitreous Humor Reveals Distinct Protein Profiles in Patients with Retinopathy of Prematurity. Invest. Ophthalmol. Vis. Sci. 2013;54(15):587.

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

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Abstract

Purpose: Retinopathy of Prematurity (ROP) is a vaso-proliferative eye disease in premature babies with low gestational age (≤32 weeks) and birth weight (≤1,700g) and is characterized by abnormal retinal vascular development. The present study aimed to evaluate the levels of inflammatory and angiogenic factors in ROP for understanding their involvement in the disease process.

Methods: Vitreous humor (50-100μl) were collected from patients (n=30) with stage IV and V of ROP (classified as per ICROP guidelines) along with infants with congenital cataract as control subjects (n=30) undergoing vitrectomy, with prior informed consent from their parents. The concentrations of 28 proteins involved in neuro-degeneration, extracellular matrix (ECM) remodeling, angiogenesis and inflammatory pathways in pre-diluted vitreous (1:5) samples were evaluated using multiplex bead immunoassays based on Luminex xMAP technology. Differences between levels of these proteins were analyzed using appropriate statistical tests followed by validations by western blotting.

Results: Of all the analytes evaluated, 21/28 could be detected in the vitreous humor of these subjects. Patients with ROP exhibited significant elevations in MMP9 (p=0.035), CFH (p=0.002), C3 (p=0.006), C4 (=0.0009), Prealbumin (p=0.012), SAP (p=0.026), APOA1 (p=0.002) and APOC3 (p=0.006) compared to the controls. The concentrations of the remaining proteins in the vitreous humor were not significantly different between the patients and controls (p>0.05).

Conclusions: The elevated levels of 8/21 proteins in the vitreous humor of patients indicated that abnormal immune environments and ECM components might play a role in the development of ROP.

Keywords: 706 retinopathy of prematurity • 660 proteins encoded by disease genes • 763 vitreous  
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