March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Enhanced depth imaging optical coherence tomography in type 2 diabetes
Author Affiliations & Notes
  • Rosangela Lattanzio
    Ophthalmology, Department of Ophthalmology University Scientific Institute San Raffaele, Milan, Italy
  • Giuseppe Querques
    Ophthalmology, Department of Ophthalmology University Scientific Institute San Raffaele, Milan, Italy
  • Lea Querques
    Ophthalmology, Department of Ophthalmology University Scientific Institute San Raffale, Milan, Italy
  • Claudia Del Turco
    Ophthalmology, Department of Ophthalmology University Scientific Institute San Raffale, Milan, Italy
  • Luisa Pierro
    Ophthalmology, Department of Ophthalmology University Scientific Institute San Raffale, Milan, Italy
  • Raimondo Forte
    Ophthalmology, Hopital Intercommunal de Creteil, University Paris- Est Creteil, France
  • Francesco Bandello
    Ophthalmology, Department of Ophthalmology University Scientific Institute San Raffale, Milan, Italy
  • Footnotes
    Commercial Relationships  Rosangela Lattanzio, None; Giuseppe Querques, None; Lea Querques, None; Claudia Del Turco, None; Luisa Pierro, None; Raimondo Forte, None; Francesco Bandello, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 2644. doi:
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      Rosangela Lattanzio, Giuseppe Querques, Lea Querques, Claudia Del Turco, Luisa Pierro, Raimondo Forte, Francesco Bandello; Enhanced depth imaging optical coherence tomography in type 2 diabetes. Invest. Ophthalmol. Vis. Sci. 2012;53(14):2644.

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

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Abstract

Purpose: : To investigate the changes in choroidal thickness within the macula of eyes with various stages of diabetic retinopathy, using enhanced depth imaging optical coherence tomography (EDI OCT).

Methods: : Sixty-three consecutive diabetic patients without (NDR) or with diabetic retinopathy (non-proliferative diabetic retinopathy [NPDR] and no clinically significant macular edema [CSME-]; NDPR and clinically significant macular edema [CSME+]) underwent EDI OCT. Twenty-one age and sex matched healthy subjects (21 eyes) also underwent EDI OCT.

Results: : A total of 63 eyes of 63 consecutive diabetic patients (26 female (41.2%); mean age 65.4 ± 8.9 years, range 48-83 years) were included in the analysis. Mean BCVA was 0.13±0.25 LogMAR (range 0-1). Mean CMT was 272.47±16.24 μm in 21 NDR eyes, 294.52±23.51 μm in 21 NPDR/CSME- eyes, and 385.61±75.07 μm in 21 NPDR/CSME+ eyes. There was no difference in mean subfoveal choroidal thickness among each diabetic group (238.42±47.95 μm [NDR], 207.0±55.95 μm [NPDR/CSME-], 190.85±48.43 μm NPDR/CSME+; p=0.18). The mean subfoveal choroidal thickness was significantly reduced in each diabetic group compared with the control group (309.76±58.52 μm, p<0.001).

Conclusions: : In diabetic eyes there is an overall thinning of the choroid on EDI OCT. A decreased choroidal thickness may lead to tissue hypoxia and consequently increase the level of VEGF, resulting in the breakdown of the blood-retinal barrier and the development of macular edema.

Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • choroid • diabetic retinopathy 
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