Volume 93, Issue S255
ABS15-0132
Free Access

The changes of the retinal layers in diabetic patiens with retinopathy

S. Vujosevic

S. Vujosevic

Ophthalmology, Neuroscience, University of Padova, Padova, Italy

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S. Bini

S. Bini

Ophthalmology, Neuroscience, University of Padova, Padova, Italy

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M. Berton

M. Berton

Ophthalmology, Neuroscience, University of Padova, Padova, Italy

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G. Midena

G. Midena

Campus Biomedico, Medicine, Roma, Italy

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F. Martini

F. Martini

Ophthalmology, Neuroscience, University of Padova, Padova, Italy

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E. Midena

E. Midena

Ophthalmology, Neuroscience, University of Padova- Fondazione G.B.Bietti IRCCS, Padova- Roma, Italy

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First published: 23 September 2015

Summary

Purpose

Retinal neurodegeneration and inflammation are considered early events in diabetic retinopathy(DR). Herein are described changes, in retinal glial and neuronal cells, with spectral domain(SD-OCT) in patients with non proliferative DR.

Methods

130 subjects were evaluated:88 diabetics with DR and 42 normals.All subjects underwent full ophthalmologic examination and SD-OCT. After automatic retinal segmentation in 5 layers, the thickness of each layer was calculated and compared. Intraretinal hyperreflective spots(HRS) were evaluated on linear scans.

Results

A significant increase in inner nuclear (INL) and outer plexiform(p < 0.01) and decrease in retinal nerve fiber layer (RNFL) thickness (p < 0.01) was found in DR eyes (without DME) vs controls.HRS number was significantly higher in diabetics with DR with or without DME vs controls,(p < 0.05). HRS number increased with progressing DR.

Conclusion

Selective thinning of inner retina in the macula, suggesting an early neuronal loss(accompanied by Muller cells activation with increased INL thickness) in DR is reported. HRS increase and migration to outer retina, may represent a surrogate of microglial activation.SD-OCT may be useful in detecting intraretinal changes in DR.

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