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A composite measure to explore visual disability in primary progressive multiple sclerosis

BACKGROUND: Optical coherence tomography (OCT) and magnetic resonance imaging (MRI) can provide complementary information on visual system damage in multiple sclerosis (MS). OBJECTIVES: The objective of this paper is to determine whether a composite OCT/MRI score, reflecting cumulative damage along...

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Autores principales: Poretto, Valentina, Petracca, Maria, Saiote, Catarina, Mormina, Enricomaria, Howard, Jonathan, Miller, Aaron, Lublin, Fred D, Inglese, Matilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439656/
https://www.ncbi.nlm.nih.gov/pubmed/28607759
http://dx.doi.org/10.1177/2055217317709620
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author Poretto, Valentina
Petracca, Maria
Saiote, Catarina
Mormina, Enricomaria
Howard, Jonathan
Miller, Aaron
Lublin, Fred D
Inglese, Matilde
author_facet Poretto, Valentina
Petracca, Maria
Saiote, Catarina
Mormina, Enricomaria
Howard, Jonathan
Miller, Aaron
Lublin, Fred D
Inglese, Matilde
author_sort Poretto, Valentina
collection PubMed
description BACKGROUND: Optical coherence tomography (OCT) and magnetic resonance imaging (MRI) can provide complementary information on visual system damage in multiple sclerosis (MS). OBJECTIVES: The objective of this paper is to determine whether a composite OCT/MRI score, reflecting cumulative damage along the entire visual pathway, can predict visual deficits in primary progressive multiple sclerosis (PPMS). METHODS: Twenty-five PPMS patients and 20 age-matched controls underwent neuro-ophthalmologic evaluation, spectral-domain OCT, and 3T brain MRI. Differences between groups were assessed by univariate general linear model and principal component analysis (PCA) grouped instrumental variables into main components. Linear regression analysis was used to assess the relationship between low-contrast visual acuity (LCVA), OCT/MRI-derived metrics and PCA-derived composite scores. RESULTS: PCA identified four main components explaining 80.69% of data variance. Considering each variable independently, LCVA 1.25% was significantly predicted by ganglion cell-inner plexiform layer (GCIPL) thickness, thalamic volume and optic radiation (OR) lesion volume (adjusted R(2) 0.328, p = 0.00004; adjusted R(2) 0.187, p = 0.002 and adjusted R(2) 0.180, p = 0.002). The PCA composite score of global visual pathway damage independently predicted both LCVA 1.25% (adjusted R(2) value 0.361, p = 0.00001) and LCVA 2.50% (adjusted R(2) value 0.323, p = 0.00003). CONCLUSION: A multiparametric score represents a more comprehensive and effective tool to explain visual disability than a single instrumental metric in PPMS.
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spelling pubmed-54396562017-06-12 A composite measure to explore visual disability in primary progressive multiple sclerosis Poretto, Valentina Petracca, Maria Saiote, Catarina Mormina, Enricomaria Howard, Jonathan Miller, Aaron Lublin, Fred D Inglese, Matilde Mult Scler J Exp Transl Clin Original Article BACKGROUND: Optical coherence tomography (OCT) and magnetic resonance imaging (MRI) can provide complementary information on visual system damage in multiple sclerosis (MS). OBJECTIVES: The objective of this paper is to determine whether a composite OCT/MRI score, reflecting cumulative damage along the entire visual pathway, can predict visual deficits in primary progressive multiple sclerosis (PPMS). METHODS: Twenty-five PPMS patients and 20 age-matched controls underwent neuro-ophthalmologic evaluation, spectral-domain OCT, and 3T brain MRI. Differences between groups were assessed by univariate general linear model and principal component analysis (PCA) grouped instrumental variables into main components. Linear regression analysis was used to assess the relationship between low-contrast visual acuity (LCVA), OCT/MRI-derived metrics and PCA-derived composite scores. RESULTS: PCA identified four main components explaining 80.69% of data variance. Considering each variable independently, LCVA 1.25% was significantly predicted by ganglion cell-inner plexiform layer (GCIPL) thickness, thalamic volume and optic radiation (OR) lesion volume (adjusted R(2) 0.328, p = 0.00004; adjusted R(2) 0.187, p = 0.002 and adjusted R(2) 0.180, p = 0.002). The PCA composite score of global visual pathway damage independently predicted both LCVA 1.25% (adjusted R(2) value 0.361, p = 0.00001) and LCVA 2.50% (adjusted R(2) value 0.323, p = 0.00003). CONCLUSION: A multiparametric score represents a more comprehensive and effective tool to explain visual disability than a single instrumental metric in PPMS. SAGE Publications 2017-05-18 /pmc/articles/PMC5439656/ /pubmed/28607759 http://dx.doi.org/10.1177/2055217317709620 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ 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 Article
Poretto, Valentina
Petracca, Maria
Saiote, Catarina
Mormina, Enricomaria
Howard, Jonathan
Miller, Aaron
Lublin, Fred D
Inglese, Matilde
A composite measure to explore visual disability in primary progressive multiple sclerosis
title A composite measure to explore visual disability in primary progressive multiple sclerosis
title_full A composite measure to explore visual disability in primary progressive multiple sclerosis
title_fullStr A composite measure to explore visual disability in primary progressive multiple sclerosis
title_full_unstemmed A composite measure to explore visual disability in primary progressive multiple sclerosis
title_short A composite measure to explore visual disability in primary progressive multiple sclerosis
title_sort composite measure to explore visual disability in primary progressive multiple sclerosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439656/
https://www.ncbi.nlm.nih.gov/pubmed/28607759
http://dx.doi.org/10.1177/2055217317709620
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