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Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis

INTRODUCTION: Retinal nerve fiber layer thickness has been used for monitoring of disease activity in patients with multiple sclerosis (MS). Macular ganglion cell complex (GCC) layer of retina also can be measured by OCT and has been suggested as a potential biomarker in MS. In this study we investi...

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Autores principales: ÖZBİLEN, Kemal Turgay, GÜNDÜZ, Tuncay, KARTAL, Selva Nur ÇUKUROVA, CEYLAN, Nihan AKSU, ERAKSOY, Mefküre, KÜRTÜNCÜ, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Noro-Psikiyatri Arsivi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419730/
https://www.ncbi.nlm.nih.gov/pubmed/34526838
http://dx.doi.org/10.29399/npa.27531
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author ÖZBİLEN, Kemal Turgay
GÜNDÜZ, Tuncay
KARTAL, Selva Nur ÇUKUROVA
CEYLAN, Nihan AKSU
ERAKSOY, Mefküre
KÜRTÜNCÜ, Murat
author_facet ÖZBİLEN, Kemal Turgay
GÜNDÜZ, Tuncay
KARTAL, Selva Nur ÇUKUROVA
CEYLAN, Nihan AKSU
ERAKSOY, Mefküre
KÜRTÜNCÜ, Murat
author_sort ÖZBİLEN, Kemal Turgay
collection PubMed
description INTRODUCTION: Retinal nerve fiber layer thickness has been used for monitoring of disease activity in patients with multiple sclerosis (MS). Macular ganglion cell complex (GCC) layer of retina also can be measured by OCT and has been suggested as a potential biomarker in MS. In this study we investigated the macular GCC and its role as a potential biomarker in patients with Multiple Sclerosis (MS). METHODS: A prospective cohort-study, subjects consisted of Relapsing-Remitting MS patients (n=62) and healthy controls (n=60). Eyes of MS patients were divided into two subgroups according to the history of the optic neuritis (ON). Standard peripapillary-RNFL and macular scan protocol, and retinal auto-segmentation of spectral-domain OCT were performed. Macular RNFL (mRNFL), ganglion cell layer (GCL), and inner plexiform layer (IPL), and GCC (the sum of these former three layers) were recorded. The macula was divided into nine sectors using the ETDRS grid (4×9=36 variables). RESULTS: In total, 50 eyes of 36 patients had previous ON attacks. 35/36 GCC parameters were thinner in MS patients and subgroups compared to the control group (p<0.05). When the eyes with and without a history of optic neuritis were compared, 25 of 36 parameters were thinner in those with ON. There were strong correlations between visual acuity-GCC parameters and EDSS scores in patients with a history of optic neuritis. However, no such relationship was found in those without an ON story. CONCLUSION: Ganglion cell complex gets thinner in patients with MS with a decreasing order of GCL, IPL, and mRNFL. The examination of GCC in detail could be a beneficial biomarker for MS.
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spelling pubmed-84197302021-09-14 Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis ÖZBİLEN, Kemal Turgay GÜNDÜZ, Tuncay KARTAL, Selva Nur ÇUKUROVA CEYLAN, Nihan AKSU ERAKSOY, Mefküre KÜRTÜNCÜ, Murat Noro Psikiyatr Ars Research Article INTRODUCTION: Retinal nerve fiber layer thickness has been used for monitoring of disease activity in patients with multiple sclerosis (MS). Macular ganglion cell complex (GCC) layer of retina also can be measured by OCT and has been suggested as a potential biomarker in MS. In this study we investigated the macular GCC and its role as a potential biomarker in patients with Multiple Sclerosis (MS). METHODS: A prospective cohort-study, subjects consisted of Relapsing-Remitting MS patients (n=62) and healthy controls (n=60). Eyes of MS patients were divided into two subgroups according to the history of the optic neuritis (ON). Standard peripapillary-RNFL and macular scan protocol, and retinal auto-segmentation of spectral-domain OCT were performed. Macular RNFL (mRNFL), ganglion cell layer (GCL), and inner plexiform layer (IPL), and GCC (the sum of these former three layers) were recorded. The macula was divided into nine sectors using the ETDRS grid (4×9=36 variables). RESULTS: In total, 50 eyes of 36 patients had previous ON attacks. 35/36 GCC parameters were thinner in MS patients and subgroups compared to the control group (p<0.05). When the eyes with and without a history of optic neuritis were compared, 25 of 36 parameters were thinner in those with ON. There were strong correlations between visual acuity-GCC parameters and EDSS scores in patients with a history of optic neuritis. However, no such relationship was found in those without an ON story. CONCLUSION: Ganglion cell complex gets thinner in patients with MS with a decreasing order of GCL, IPL, and mRNFL. The examination of GCC in detail could be a beneficial biomarker for MS. Noro-Psikiyatri Arsivi 2021-08-26 /pmc/articles/PMC8419730/ /pubmed/34526838 http://dx.doi.org/10.29399/npa.27531 Text en Copyright: © 2020 Turkish Neuropsychiatric Society https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
ÖZBİLEN, Kemal Turgay
GÜNDÜZ, Tuncay
KARTAL, Selva Nur ÇUKUROVA
CEYLAN, Nihan AKSU
ERAKSOY, Mefküre
KÜRTÜNCÜ, Murat
Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis
title Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis
title_full Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis
title_fullStr Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis
title_full_unstemmed Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis
title_short Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis
title_sort detailed evaluation of macular ganglion cell complex in patients with multiple sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419730/
https://www.ncbi.nlm.nih.gov/pubmed/34526838
http://dx.doi.org/10.29399/npa.27531
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