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Relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis

PURPOSE: This study aimed to identify an easy-to-apply biomarker by correlating visual evoked potential (VEP) with optical coherence tomography angiography (OCTA) results in multiple sclerosis (MS). METHODS: Our study was planned prospectively. Patients with MS were divided into two groups, VEP prol...

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Autores principales: Ava, Sedat, Tamam, Yusuf, Hazar, Leyla, Karahan, Mine, Erdem, Seyfettin, Dursun, Mehmet Emin, Keklikçi, Ugur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114564/
https://www.ncbi.nlm.nih.gov/pubmed/35225535
http://dx.doi.org/10.4103/ijo.IJO_431_21
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author Ava, Sedat
Tamam, Yusuf
Hazar, Leyla
Karahan, Mine
Erdem, Seyfettin
Dursun, Mehmet Emin
Keklikçi, Ugur
author_facet Ava, Sedat
Tamam, Yusuf
Hazar, Leyla
Karahan, Mine
Erdem, Seyfettin
Dursun, Mehmet Emin
Keklikçi, Ugur
author_sort Ava, Sedat
collection PubMed
description PURPOSE: This study aimed to identify an easy-to-apply biomarker by correlating visual evoked potential (VEP) with optical coherence tomography angiography (OCTA) results in multiple sclerosis (MS). METHODS: Our study was planned prospectively. Patients with MS were divided into two groups, VEP prolonged group 1 and VEP normal group 2. Age-matched and gender-matched healthy individuals (group 3) were included as the control group. Vascular density (VD) of the optic nerve head (ONH) and radial peripapillary capillaries (RPCs) were measured and recorded by OCTA. The optic nerve damage of patients was measured and recorded with a VEP device. RESULTS: Thirty-two eyes were included in group 1, 50 eyes were included in group 2, and 51 healthy eyes were included in group 3. In terms of visual acuity, group 1 was significantly lower than the other groups (P < 0.001). Regardless of the prolongation of p100 latency in patients with MS, whole image, inside disc ONH VD and in the same sectors in RPC VD were found to be significantly lower than the control group (P < 0.05). Retinal nerve fiber layer thickness was found to be significantly lower in group 1 than in group 2 and group 3 (P < 0.05). There was a significant correlation between low ONH VD and RPC VD and prolonged VEP P100 (P < 0.05). CONCLUSION: VEP measurements can be correlated with OCTA measurements in patients with MS and can be used as a biomarker to determine the degree of optic nerve damage.
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spelling pubmed-91145642022-05-19 Relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis Ava, Sedat Tamam, Yusuf Hazar, Leyla Karahan, Mine Erdem, Seyfettin Dursun, Mehmet Emin Keklikçi, Ugur Indian J Ophthalmol Special Focus, Retina, Original Article PURPOSE: This study aimed to identify an easy-to-apply biomarker by correlating visual evoked potential (VEP) with optical coherence tomography angiography (OCTA) results in multiple sclerosis (MS). METHODS: Our study was planned prospectively. Patients with MS were divided into two groups, VEP prolonged group 1 and VEP normal group 2. Age-matched and gender-matched healthy individuals (group 3) were included as the control group. Vascular density (VD) of the optic nerve head (ONH) and radial peripapillary capillaries (RPCs) were measured and recorded by OCTA. The optic nerve damage of patients was measured and recorded with a VEP device. RESULTS: Thirty-two eyes were included in group 1, 50 eyes were included in group 2, and 51 healthy eyes were included in group 3. In terms of visual acuity, group 1 was significantly lower than the other groups (P < 0.001). Regardless of the prolongation of p100 latency in patients with MS, whole image, inside disc ONH VD and in the same sectors in RPC VD were found to be significantly lower than the control group (P < 0.05). Retinal nerve fiber layer thickness was found to be significantly lower in group 1 than in group 2 and group 3 (P < 0.05). There was a significant correlation between low ONH VD and RPC VD and prolonged VEP P100 (P < 0.05). CONCLUSION: VEP measurements can be correlated with OCTA measurements in patients with MS and can be used as a biomarker to determine the degree of optic nerve damage. Wolters Kluwer - Medknow 2022-03 2022-02-25 /pmc/articles/PMC9114564/ /pubmed/35225535 http://dx.doi.org/10.4103/ijo.IJO_431_21 Text en Copyright: © 2022 Indian Journal of Ophthalmology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Special Focus, Retina, Original Article
Ava, Sedat
Tamam, Yusuf
Hazar, Leyla
Karahan, Mine
Erdem, Seyfettin
Dursun, Mehmet Emin
Keklikçi, Ugur
Relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis
title Relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis
title_full Relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis
title_fullStr Relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis
title_full_unstemmed Relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis
title_short Relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis
title_sort relationship between optical coherence tomography angiography and visual evoked potential in patients with multiple sclerosis
topic Special Focus, Retina, Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114564/
https://www.ncbi.nlm.nih.gov/pubmed/35225535
http://dx.doi.org/10.4103/ijo.IJO_431_21
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