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Early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis
BACKGROUND: Biomarkers are urgently required for predicting the likely progression of multiple sclerosis (MS) at the earliest stages of the disease to aid in personalised therapy. OBJECTIVE: We aimed to examine early brain volumetric and microstructural changes and retinal nerve fibre layer thinning...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651676/ https://www.ncbi.nlm.nih.gov/pubmed/31384479 http://dx.doi.org/10.1177/2055217319863122 |
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author | Gajamange, Sanuji Stankovich, Jim Egan, Gary Kilpatrick, Trevor Butzkueven, Helmut Fielding, Joanne van der Walt, Anneke Kolbe, Scott |
author_facet | Gajamange, Sanuji Stankovich, Jim Egan, Gary Kilpatrick, Trevor Butzkueven, Helmut Fielding, Joanne van der Walt, Anneke Kolbe, Scott |
author_sort | Gajamange, Sanuji |
collection | PubMed |
description | BACKGROUND: Biomarkers are urgently required for predicting the likely progression of multiple sclerosis (MS) at the earliest stages of the disease to aid in personalised therapy. OBJECTIVE: We aimed to examine early brain volumetric and microstructural changes and retinal nerve fibre layer thinning as predictors of longer term MS severity in patients with clinically isolated syndromes (CIS). METHODS: Lesion metrics, brain and regional atrophy, diffusion fractional anisotropy and retinal nerve fibre layer thickness were prospectively assessed in 36 patients with CIS over the first 12 months after presentation and compared with clinical outcomes at longer term follow-up [median (IQR) = 8.5 (7.8–8.9) years]. RESULTS: In total, 25 (69%) patients converted to MS and had greater baseline lesion volume (p = 0.008) and number (p = 0.03)than CIS patients. Over the initial 12 months, new lesions (p = 0.0001), retinal nerve fibre layer thinning (p = 0.04) and ventricular enlargement (p = 0.03) were greater in MS than CIS patients. In MS patients, final Expanded Disability Status Scale score correlated with retinal nerve fibre layer thinning over the first 12 months (ρ = −0.67, p = 0.001). CONCLUSIONS: Additional to lesion metrics, early measurements of fractional anisotropy and retinal nerve fibre layer thinning are informative about longer term clinical outcomes in CIS. |
format | Online Article Text |
id | pubmed-6651676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-66516762019-08-05 Early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis Gajamange, Sanuji Stankovich, Jim Egan, Gary Kilpatrick, Trevor Butzkueven, Helmut Fielding, Joanne van der Walt, Anneke Kolbe, Scott Mult Scler J Exp Transl Clin Original Research Paper BACKGROUND: Biomarkers are urgently required for predicting the likely progression of multiple sclerosis (MS) at the earliest stages of the disease to aid in personalised therapy. OBJECTIVE: We aimed to examine early brain volumetric and microstructural changes and retinal nerve fibre layer thinning as predictors of longer term MS severity in patients with clinically isolated syndromes (CIS). METHODS: Lesion metrics, brain and regional atrophy, diffusion fractional anisotropy and retinal nerve fibre layer thickness were prospectively assessed in 36 patients with CIS over the first 12 months after presentation and compared with clinical outcomes at longer term follow-up [median (IQR) = 8.5 (7.8–8.9) years]. RESULTS: In total, 25 (69%) patients converted to MS and had greater baseline lesion volume (p = 0.008) and number (p = 0.03)than CIS patients. Over the initial 12 months, new lesions (p = 0.0001), retinal nerve fibre layer thinning (p = 0.04) and ventricular enlargement (p = 0.03) were greater in MS than CIS patients. In MS patients, final Expanded Disability Status Scale score correlated with retinal nerve fibre layer thinning over the first 12 months (ρ = −0.67, p = 0.001). CONCLUSIONS: Additional to lesion metrics, early measurements of fractional anisotropy and retinal nerve fibre layer thinning are informative about longer term clinical outcomes in CIS. SAGE Publications 2019-07-23 /pmc/articles/PMC6651676/ /pubmed/31384479 http://dx.doi.org/10.1177/2055217319863122 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Paper Gajamange, Sanuji Stankovich, Jim Egan, Gary Kilpatrick, Trevor Butzkueven, Helmut Fielding, Joanne van der Walt, Anneke Kolbe, Scott Early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis |
title | Early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis |
title_full | Early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis |
title_fullStr | Early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis |
title_full_unstemmed | Early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis |
title_short | Early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis |
title_sort | early imaging predictors of longer term multiple sclerosis risk and severity in acute optic neuritis |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651676/ https://www.ncbi.nlm.nih.gov/pubmed/31384479 http://dx.doi.org/10.1177/2055217319863122 |
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