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Erschienen in: Journal of Neurology 11/2016

20.08.2016 | Original Communication

Retinal measures correlate with cognitive and physical disability in early multiple sclerosis

verfasst von: Nabil K. El Ayoubi, Stephanie Ghassan, Marianne Said, Joelle Allam, Hala Darwish, Samia J. Khoury

Erschienen in: Journal of Neurology | Ausgabe 11/2016

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Abstract

Further studies are needed to determine the role of retinal optical coherence tomography (OCT) in non-optic neuritis (ON) eyes of patients with early MS. The objective of this study is to explore the relationship between retinal layers’ thickness and cognitive as well as physical disability in patients with the early RRMS. Participants in this cross-sectional study were adults with early RRMS, stable on interferon beta-1a, or fingolimod therapy, and without a history of ON in one or both eyes. Patients were evaluated clinically, underwent a battery of cognitive tests, and a retinal OCT scan which was also performed on a group of healthy age- and gender-matched controls. We studied 47 patients with RRMS, on interferon beta-1a (N = 32) or fingolimod (N = 15), and 18 healthy controls. Multivariate analyses controlling for age, disease duration, treatment, and education when exploring cognitive function, showed that pRNFL thickness correlated negatively with 9HPT (standardized Beta −0.4, p < 0.0001), and positively with SDMT (standardized Beta 0.72, p = 0.007). In patients with early RRMS without optic neuropathy, retinal thickness measures correlated with physical disability and cognitive disability, supporting their potential as biomarkers of axonal loss.
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Metadaten
Titel
Retinal measures correlate with cognitive and physical disability in early multiple sclerosis
verfasst von
Nabil K. El Ayoubi
Stephanie Ghassan
Marianne Said
Joelle Allam
Hala Darwish
Samia J. Khoury
Publikationsdatum
20.08.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Neurology / Ausgabe 11/2016
Print ISSN: 0340-5354
Elektronische ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-016-8271-4

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