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Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy
Previously not shown this study support that mfVEP is an indicator of optic nerve neuropathy in diabetic patients and there could be a correlation between the optic nerve dysfunction and diabetic poly neuropathy. The early optic nerve involvement might explain some of the visual complain in this gro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Open
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504721/ https://www.ncbi.nlm.nih.gov/pubmed/23198007 http://dx.doi.org/10.2174/1874364101206010098 |
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author | Lövestam-Adrian, Monica Gränse, Lotta Andersson, Gert Andreasson, Sten |
author_facet | Lövestam-Adrian, Monica Gränse, Lotta Andersson, Gert Andreasson, Sten |
author_sort | Lövestam-Adrian, Monica |
collection | PubMed |
description | Previously not shown this study support that mfVEP is an indicator of optic nerve neuropathy in diabetic patients and there could be a correlation between the optic nerve dysfunction and diabetic poly neuropathy. The early optic nerve involvement might explain some of the visual complain in this group of diabetic patients. PURPOSE: To investigate the function of the visual pathway measured by mfVEP (multifocal Visual Evoked Potentials) in patients with diabetic retinopathy and neurophysiologically verified polyneuropathy SUBJECTS AND METHODS: Thirty-two diabetic patients with the same degree of diabetic retinopathy were classified with neurography regarding polyneuropathy and further examined with mfVEP. The mfVEPs of eighteen patients with polyneuropathy were compared to those of fourteen diabetic patients without polyneuropathy and to those of ten nondiabetic subjects. RESULTS: Diabetic duration, and the number of patients who had undergone panretinal photocoagulation for proliferative diabetic retinopathy were similar in the two patient groups, 29±13 vs 25±7 years, p=0.3. Both groups of patients with diabetic retinopathy had significantly lower amplitudes in the mfVEP than the healthy subjects. In addition the mfVEP amplitudes, which reflect selected areas of the visual function, were significantly reduced in the lower nasal quadrant in patients with neuropathy compared to patients without neuropathy. CONCLUSION: The results indicate that mfVEP could be an indicator of optic nerve neuropathy in patients with diabetic retinopathy. The early optic nerve involvement might explain some of the visual complaints in this group of diabetic patients. |
format | Online Article Text |
id | pubmed-3504721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-35047212012-11-29 Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy Lövestam-Adrian, Monica Gränse, Lotta Andersson, Gert Andreasson, Sten Open Ophthalmol J Article Previously not shown this study support that mfVEP is an indicator of optic nerve neuropathy in diabetic patients and there could be a correlation between the optic nerve dysfunction and diabetic poly neuropathy. The early optic nerve involvement might explain some of the visual complain in this group of diabetic patients. PURPOSE: To investigate the function of the visual pathway measured by mfVEP (multifocal Visual Evoked Potentials) in patients with diabetic retinopathy and neurophysiologically verified polyneuropathy SUBJECTS AND METHODS: Thirty-two diabetic patients with the same degree of diabetic retinopathy were classified with neurography regarding polyneuropathy and further examined with mfVEP. The mfVEPs of eighteen patients with polyneuropathy were compared to those of fourteen diabetic patients without polyneuropathy and to those of ten nondiabetic subjects. RESULTS: Diabetic duration, and the number of patients who had undergone panretinal photocoagulation for proliferative diabetic retinopathy were similar in the two patient groups, 29±13 vs 25±7 years, p=0.3. Both groups of patients with diabetic retinopathy had significantly lower amplitudes in the mfVEP than the healthy subjects. In addition the mfVEP amplitudes, which reflect selected areas of the visual function, were significantly reduced in the lower nasal quadrant in patients with neuropathy compared to patients without neuropathy. CONCLUSION: The results indicate that mfVEP could be an indicator of optic nerve neuropathy in patients with diabetic retinopathy. The early optic nerve involvement might explain some of the visual complaints in this group of diabetic patients. Bentham Open 2012-11-16 /pmc/articles/PMC3504721/ /pubmed/23198007 http://dx.doi.org/10.2174/1874364101206010098 Text en © Lövestam-Adrian et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Lövestam-Adrian, Monica Gränse, Lotta Andersson, Gert Andreasson, Sten Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy |
title | Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy |
title_full | Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy |
title_fullStr | Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy |
title_full_unstemmed | Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy |
title_short | Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy |
title_sort | multifocal visual evoked potentials (mfvep) in diabetic patients with and without polyneuropathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504721/ https://www.ncbi.nlm.nih.gov/pubmed/23198007 http://dx.doi.org/10.2174/1874364101206010098 |
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