ARVO Meeting Abstracts
 QUICK SEARCH:   [advanced]


This Article
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yanni, S. E.
Right arrow Articles by Birch, E. E.
Right arrow Search for Related Content
Right arrow Articles by Yanni, S. E.
Right arrow Articles by Birch, E. E.
Invest Ophthalmol Vis Sci 2011;52: E-Abstract 3133.
© 2011 ARVO


Foveal Avascular Zone and Foveal Pit Formation in Regressed ROP

Susan E. Yanni1, Jingyun Wang1, Melody Chan2, Joseph Carroll3, Sina Farsiu2, Joel N. Leffler4 and Eileen E. Birch1,4

1Retina Foundation of the Southwest, Dallas, Texas
2Biomedical Engineering, Duke University, Durham, North Carolina
3Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin
4Ophthalmology, UT Southwestern Medical Center, Dallas, Texas

Commercial Relationships: Susan E. Yanni, None; Jingyun Wang, None; Melody Chan, None; Joseph Carroll, None; Sina Farsiu, None; Joel N. Leffler, None; Eileen E. Birch, None

Support: Gerber Foundation, Once Upon A Time Foundation, OneSight Foundation


Purpose:Vascularization of the macula takes place between 24-27 weeks gestational age (GA). Preterm birth, and the resultant change in retinal pO2, may affect the developmental interactions among formation of a vascular plexus around the foveal avascular zone (FAZ), formation of the foveal depression, and displacement of inner retinal layers away from the incipient fovea. Previously, we showed that birth before 28 weeks GA resulted in a failure of the inner retinal neurons to migrate away from the fovea. Here we examined whether foveal vascular abnormalities accompany the inner retinal abnormality, and whether they are coincident.

Methods:SD-OCT volume scans were obtained from 11 children with regressed ROP (normal-appearing posterior poles; 23-27 wk GA; age range, 5-15 yrs) and 12 full-term controls (age range, 7-16 yrs). A custom-designed Matlab program was used to measure total retinal thickness and the thickness of individual retinal layers (Hood et al., IOVS, 2009). SD-OCT data were also fit using a mathematical model designed to capture the contour of the foveal surface, and metrics of foveal morphology were extracted (depth, diameter, slope). Summed voxel projections for the GCL-INL were used to identify the FAZ.

Results:Despite similar foveal diameters (1857.1±66.4 NML vs 1705.1±234.9 um ROP), children with regressed ROP had significantly smaller FAZ diameters than controls (443.5±69.5 vs 818.0±236.1 um; p<0.001).The foveas of ROP children were significantly shallower (p<0.001) and total retinal thickness at the fovea was significantly increased (p<0.001) compared to controls. The GCL-IPL thickness was significantly (p<0.02) thicker in ROP children at the fovea through 400 um, but not at >800 um. FAZ diameter was negatively correlated with total foveal thickness (r2=0.40) and GCL-IPL thickness at the fovea (r2 = 0.61). No significant differences in IS or OS thickness, or ONL ratios were found between ROP children and controls.

Conclusions:Preterm birth results in abnormal foveal vascularization and a failure of the inner retinal neurons to migrate away from the fovea. Despite a small FAZ and shallow foveal pit, there were no detectable abnormalities in foveal cone packing or cone length. These findings suggest that the neurovascular interactions involved in foveal pit formation may not be linked to the centripetal forces that lead to cone packing.

Keywords: retinopathy of prematurity • imaging/image analysis: clinical • macula/fovea

© 2011, The Association for Research in Vision and Ophthalmology, Inc., all rights reserved. Permission to republish any abstract or part of an abstract in any form must be obtained in writing from the ARVO Office prior to publication.