May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
Postnatal Brain Growth in Premature Infants Parallels and Predicts Retinopathy of Prematurity
Author Affiliations & Notes
  • L.H. Smith
    Ophthalmology–Fegan 4, Harvard Med School/Childrens, Boston, MA
  • J. Sigurdsson
    Pediatrics, Göteborg Pediatric Growth Research Center,, The Queen Silvia Children’s Hospital, Göteborg, Sweden
  • E. Engström
    Pediatrics,
    Göteborg Pediatric Growth Research Center, The Queen Silvia Children’s Hospital, Göteborg, Sweden
  • C. Löfqvist
    Pediatrics,
    Göteborg Pediatric Growth Research Center, The Queen Silvia Children’s Hospital, Göteborg, Sweden
  • A.–L. Hård
    Ophthalmology, Department of Clinical Neurosciences, The Queen Silvia Children’s Hospital, Göteborg, Sweden
  • A. Niklasson
    Pediatrics,
    Göteborg Pediatric Growth Research Center, The Queen Silvia Children’s Hospital, Göteborg, Sweden
  • A. Hellström
    Ophthalmology,
    Göteborg Pediatric Growth Research Center, The Queen Silvia Children’s Hospital, Göteborg, Sweden
  • Footnotes
    Commercial Relationships  L.H. Smith, None; J. Sigurdsson, None; E. Engström, None; C. Löfqvist, None; A. Hård, None; A. Niklasson, None; A. Hellström, None.
  • Footnotes
    Support  NIH EY14811, EY008670 , V Kann Rasmussen Found., Göteborg Med. Soc., Med. Res. Council
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 3495. doi:
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      L.H. Smith, J. Sigurdsson, E. Engström, C. Löfqvist, A.–L. Hård, A. Niklasson, A. Hellström; Postnatal Brain Growth in Premature Infants Parallels and Predicts Retinopathy of Prematurity . Invest. Ophthalmol. Vis. Sci. 2005;46(13):3495.

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

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Abstract

Abstract: : Purpose: An early manifestation of many diseases is loss or proliferation of blood vessels. Serum vascular markers have recently been found to predict later onset of type 2 diabetes. A larger array of vascular markers is likely to allow more specific detection of many diseases. Our aim was to determine novel retinal vascular markers for possible early detection of eye disease Methods: P7 mice exposed to hyperoxia have extensive loss of retinal vessels without initial loss of neural retina. Gene expression changes at P7–P12 between age–matched normal retina and retina with hyperoxia–induced vascular loss (reflecting primarily vessel loss) were examined with Affymetrix microarrays. Data was analyzed using a new Bayesian method to determine sources of noise in the microarray data to predict which genes would validate with real time RT–PCR. Results: Twelve genes were found which validated with real time RT–PCR and had decreased expression with vascular loss, increased expression with vaso–proliferation and were expressed in endothelial or smooth muscle cell culture. These were transmembrane 4 superfamily member 1 (Tm4sf1); basigin (Bsg); claudin–5 (Cldn5); EGF, latrophilin seven transmembrane domain containing 1 (Eltd1); occludin (Ocln); biglycan (Bgn); matrix gamma–carboxyglutamate protein (Mglap); macrophage migration inhibitory factor (Mif); neural precursor cell expressed, developmentally down–regulated gene 4–like (Nedd4l); regulator of G–protein signaling 5 (Rgs5); PDZ and LIM domain 3 (Pdlim3). Conclusions: Expression changes in these genes are predictive of vessel loss and re–growth and are potential surrogate markers of early changes in eye diseases such as diabetic retinopathy or cancer

Keywords: retinopathy of prematurity • neovascularization • retinal neovascularization 
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