Oxford Autoimmune Neurology Group

Author Of 1 Presentation

Neuropsychology and Cognition Poster Presentation

P0824 - Serum neurofilaments and Cognition in Secondary Progressive Multiple Sclerosis (ID 1639)

Speakers
Presentation Number
P0824
Presentation Topic
Neuropsychology and Cognition

Abstract

Background

Cognitive dysfunction is common in multiple sclerosis (MS) and is particularly prevalent in patients with progressive forms of the disease [1]. Exploring neurofilament associations has clear value in trying to develop treatments for cognition.

Objectives

To perform a post-hoc analysis of the MS-STAT trial [2], assessing serum neurofilament light (sNFL) and heavy (sNFH) as predictive biomarkers of future cognitive performance.

Methods

Serum samples were analysed for sNFL and sNFH using Single Molecule Array (Simoa). Cognition was assessed at months 0, 12 and 24 with a detailed neuropsychometric battery including the Wechsler Abbreviated Scale of Intelligence (WASI) and Brain Injury Rehabilitation Trust Memory and Information Processing Battery (BMIPB), as previously described [3]. Multivariate regression models were used for cross-sectional analysis, and linear mixed models were used to assess the predictive value of dichotomised baseline sNFL and sNFH on changes in cognition. All analyses controlled for the established MRI variables of whole brain volume (WBV) and T2 lesion volume (T2LV) in order to assess the extent to which sNFL and sNFH provided additional prognostic value.

Results

Cross-sectional analyses:

After adjusting for demographics, T2LV and WBV, neither sNFL nor sNFH demonstrated cross-sectional associations with current cognitive performance.

Longitudinal analyses:

Patients with high baseline sNFL experienced significantly greater cognitive decline from 0 to 24 months in WASI full-scale IQ (95% CI of coefficient -0.238 to -0.024), WASI Verbal IQ (-0.281 to -0.011), and in both immediate and delayed BMIPB figure recall (-0.489 to -0.046 and -0.399 to -0.025, respectively). sNFH was not associated with changes in cognitive performance.

Conclusions

Our results demonstrate the prognostic value of sNFL on future changes in cognitive performance in SPMS, assessed through a detailed neuropsychometric battery. sNFL remained significantly associated with future cognitive decline whilst controlling for established MRI biomarkers, suggesting that it may provide additional utility in identifying those who may benefit most from interventions aimed at preventing cognitive decline.

1. Sumowski JF et al (2018) Cognition in multiple sclerosis: State of the field and priorities for the future. Neurology

2. Chataway J et al (2014) Effect of high-dose simvastatin on brain atrophy and disability in secondary progressive multiple sclerosis (MS-STAT): a randomised, placebo-controlled, phase 2 trial. Lancet

3. Chan D et al (2017) Effect of high-dose simvastatin on cognitive, neuropsychiatric, and health-related quality-of-life measures in secondary progressive multiple sclerosis: secondary analyses from the MS-STAT randomised, placebo-controlled trial. Lancet Neurol

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