rss
Br J Ophthalmol doi:10.1136/bjo.2006.111534

Decreased OCT-measured pericentral retinal thickness in patients with diabetes mellitus type 1 with minimal diabetic retinopathy

  1. Carine Biallosterski (c.biallosterski{at}amc.uva.nl),
  2. Mirjam EJ van Velthoven (m.e.vanvelthoven{at}amc.uva.nl),
  3. Robert PJ Michels (r.p.michels{at}amc.uva.nl),
  4. Reinier O Schlingemann (r.schlingemann{at}amc.uva.nl),
  5. J Hans DeVries (j.h.devries{at}amc.uva.nl),
  6. Frank D Verbraak (f.d.verbraak{at}amc.uva.nl)
  1. Academic Medical Centre, Netherlands
  2. Academic Medical Centre, Netherlands
  3. Academic Medical Centre, Netherlands
  4. Academic Medical Centre, Netherlands
  5. Academic Medical Centre, Netherlands
  6. Academic Medical Centre, Netherlands
    • Published Online First 23 March 2007

    Abstract

    Aim: A comparison of retinal thickness (RT) measurements with optical coherence tomography (OCT) in patients with type 1 diabetes mellitus (DM) and no or minimal diabetic retinopathy (DR) versus healthy controls.

    Methods: Fifty-three patients with type 1 DM with no or minimal DR underwent full ophthalmic examination, fundus photography and OCT. Mean RT measured by OCT was calculated for the central fovea, the fovea, the pericentral, and the peripheral area of the macula and compared to normal controls.

    Results: Mean RT in the pericentral area was lower in patients with minimal DR (267μm ± 20μm; n=23) compared to healthy subjects (281μm ± 13μm; P value = 0.005; n=28). Mean pericentral RT in patients without DR (276μm ± 14μm; n=30) was less than pericentral RT in normal controls, but higher than in patients with minimal DR, without being statistically significant. None of the other regions showed a significant change.

    Conclusion: In this study a significantly decreased pericentral RT was measured in patients with minimal DR compared to healthy controls. This could be explained by a loss of intraretinal neural tissue in the earliest stage of DR.

    Relevant Article

    This Article

    1. All Versions of this Article:
      1. bjo.2006.111534v1
      2. 91/9/1135 most recent

    Services

    1. Request permissions

    Responses

    1. Submit a response
    2. No responses published

    Social bookmarking

    Register for free content


    Free sample
    This recent issue is free to all users to allow everyone the opportunity to see the full scope and typical content of BJO.
    View free sample issue >>

    Free archive
    The full back archive is now available for BJO. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006, back to volume 1 issue 1.
    Register to access the free archive >>

    Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.