November 1997
Volume 38, Issue 12
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Articles  |   November 1997
Mapping of retinal function in diabetic retinopathy using the multifocal electroretinogram.
Author Affiliations
  • A M Palmowski
    Smith-Kettlewell Eye Research Institute, San Francisco, CA 94115, USA.
  • E E Sutter
    Smith-Kettlewell Eye Research Institute, San Francisco, CA 94115, USA.
  • M A Bearse, Jr
    Smith-Kettlewell Eye Research Institute, San Francisco, CA 94115, USA.
  • W Fung
    Smith-Kettlewell Eye Research Institute, San Francisco, CA 94115, USA.
Investigative Ophthalmology & Visual Science November 1997, Vol.38, 2586-2596. doi:
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    • Get Citation

      A M Palmowski, E E Sutter, M A Bearse, W Fung; Mapping of retinal function in diabetic retinopathy using the multifocal electroretinogram.. Invest. Ophthalmol. Vis. Sci. 1997;38(12):2586-2596.

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

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Abstract

PURPOSE: To investigate focal abnormalities in the electroretinogram (ERG) signal in diabetic patients, with and without retinopathy, using a multifocal ERG. METHODS: Sixteen patients with diabetes mellitus, 8 of whom had diabetic retinopathy (mean duration of diabetes: 18.5 years) and 19 approximately age-matched healthy volunteers underwent multifocal ERG testing. One hundred three retinal locations within the central 50 degrees were stimulated concurrently, according to a pseudorandom m-sequence. Response components were extracted for each stimulated retinal location. RESULTS: In diabetic patients with retinopathy, the overall amplitudes were reduced (P < 0.01), and peak implicit times were increased (P < 0.01) in the first-order component (mean flash response) and in the first slice of the second-order component (local two flash interaction). In addition, local reductions of amplitude could be seen in the first- and second-order components. In patients without retinopathy, only amplitudes of the second-order component were reduced (P < 0.01). Another salient difference was observed in a special feature of the second-order component that was reduced in diabetic patients, with and without retinopathy (P < 0.05). CONCLUSIONS: Second-order components depend on nonlinear dynamics. Thus our findings indicate changes in the nonlinear dynamics of a fast-gain control in diabetic patients, presumably located in the inner retina. This suggests that early functional changes of the inner retina are evident in diabetic patients before impairment of the outer retina is observed. Multifocal nonlinear analysis permits the detection of subclinical diabetic retinopathy and offers the advantage of topographic mapping of retinal dysfunction.

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