2017
DOI: 10.1212/wnl.0000000000004736
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No evidence of disease activity is associated with reduced rate of axonal retinal atrophy in MS

Abstract: NEDA is associated with a relatively preserved RNFL over 2 years. A greater neuroretinal loss was detected even in patients with clinical evidence of disease activity independently from changes in brain MRI lesions, prompting further validation of OCT as an additional tool in MS monitoring.

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Cited by 37 publications
(30 citation statements)
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“…We detected RNFL thinning on OCT in 56% of MS‐ON eyes and 75% of Ab‐ON eyes, similar to a recent study identifying RNFL thinning in 50% of children with multiple sclerosis and a history of optic neuritis . OCT offers an opportunity to monitor disease activity and progression non‐invasively; in adults with multiple sclerosis, RNFL thinning is a sensitive and specific predictor of clinical disease activity, independent of lesion accumulation on brain MRI . However, it is not yet part of routine clinical practice across all paediatric centres, and robust control data in typically developing children remain limited, as is standardization of RNFL measurements, particularly in the acute phase of optic neuritis when swelling may complicate some automated RNFL measures.…”
Section: Discussionsupporting
confidence: 81%
“…We detected RNFL thinning on OCT in 56% of MS‐ON eyes and 75% of Ab‐ON eyes, similar to a recent study identifying RNFL thinning in 50% of children with multiple sclerosis and a history of optic neuritis . OCT offers an opportunity to monitor disease activity and progression non‐invasively; in adults with multiple sclerosis, RNFL thinning is a sensitive and specific predictor of clinical disease activity, independent of lesion accumulation on brain MRI . However, it is not yet part of routine clinical practice across all paediatric centres, and robust control data in typically developing children remain limited, as is standardization of RNFL measurements, particularly in the acute phase of optic neuritis when swelling may complicate some automated RNFL measures.…”
Section: Discussionsupporting
confidence: 81%
“…It should be considered for inclusion in composite measures assessing disease activity in clinical trials and routine practice. This is underlined by a recent study showing that loss of pRNFL is reduced in patients showing no evidence of disease activity and is able to correctly classify no evidence of disease activity status in a significant proportion of patients .…”
Section: Discussionmentioning
confidence: 91%
“…Therefore, we cannot conclude that increased axonal damage corresponds to a higher disability. Similarly, other authors were also unable to demonstrate this association (Henderson et al, ; Oreja‐Guevara, Noval, Manzano, & Diez‐Tejedor, ), although recent studies established a relationship between RNFL thickness and risk of disability progression (Martínez‐Lapiscina et al, ), and rate of RNFL thinning and NEDA‐3 at 2 years (AUC = 0.8) (Pisa et al, ) There may be multiple reasons for this, including the short follow‐up period, patient heterogeneity, the small sample sizes used in most studies, or perhaps because EDSS is not sensitive enough to detect changes in disability when there is no motor impairment. Therefore, future studies should aim to use larger sample sizes, longer follow‐up times, and more sensitive scales capable of detecting subtler changes in disability.…”
Section: Discussionmentioning
confidence: 99%