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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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Detalles Bibliográficos
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
Descripción
Sumario: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.