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Review

Current Status of Oral Disease-Modifying Treatment Effects on Cognitive Outcomes in Multiple Sclerosis: A Scoping Review

by
Vincenzo Carlomagno
1,2,
Massimiliano Mirabella
1,2 and
Matteo Lucchini
1,2,*
1
Fondazione Policlinico Universitario Agostino Gemelli IRCCS, UOC Neurologia, 00168 Rome, Italy
2
Department of Neuroscience, Università Cattolica del Sacro Cuore, Centro di ricerca Sclerosi Multipla (CERSM), 00168 Rome, Italy
*
Author to whom correspondence should be addressed.
Bioengineering 2023, 10(7), 848; https://doi.org/10.3390/bioengineering10070848
Submission received: 10 May 2023 / Revised: 30 June 2023 / Accepted: 10 July 2023 / Published: 18 July 2023
(This article belongs to the Special Issue Cognitive Impairment in Multiple Sclerosis)

Abstract

Introduction. Cognitive impairment represents one of the most hidden and disabling clinical aspects of multiple sclerosis (MS). In this regard, the major challenges are represented by the need for a comprehensive and standardised cognitive evaluation of each patient, both at disease onset and during follow-up, and by the lack of clear-cut data on the effects of treatments. In the present review, we summarize the current evidence on the effects of the available oral disease-modifying treatments (DMTs) on cognitive outcome measures. Materials and Methods. In this systematised review, we extract all the studies that reported longitudinally acquired cognitive outcome data on oral DMTs in MS patients. Results. We found 29 studies that evaluated at least one oral DMT, including observational studies, randomised controlled trials, and their extension studies. Most of the studies (n = 20) evaluated sphingosine-1-phosphate (S1P) modulators, while we found seven studies on dimethyl fumarate, six on teriflunomide, and one on cladribine. The most frequently used cognitive outcome measures were SDMT and PASAT. Most of the studies reported substantial stability or mild improvement in cognitive outcomes in a short-time follow-up (duration of most studies ≤2 years). A few studies also reported MRI measures of brain atrophy. Conclusion. Cognitive outcomes were evaluated only in a minority of prospective studies on oral DMTs in MS patients with variable findings. More solid and numerous data are present for the S1P modulators. A standardised cognitive evaluation remains a yet unmet need to better clarify the possible positive effect of oral DMTs on cognition.
Keywords: multiple sclerosis; cognitive impairment; fingolimod; siponimod; ozanimod; cladribine; dimethyl fumarate; teriflunomide; symbol digit modality test; SDMT; paced auditory serial addition task; PASAT; Brief International Cognitive Assessment for MS; BICAMS; neuropsychological assessment; magnetic resonance imaging (MRI) multiple sclerosis; cognitive impairment; fingolimod; siponimod; ozanimod; cladribine; dimethyl fumarate; teriflunomide; symbol digit modality test; SDMT; paced auditory serial addition task; PASAT; Brief International Cognitive Assessment for MS; BICAMS; neuropsychological assessment; magnetic resonance imaging (MRI)

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MDPI and ACS Style

Carlomagno, V.; Mirabella, M.; Lucchini, M. Current Status of Oral Disease-Modifying Treatment Effects on Cognitive Outcomes in Multiple Sclerosis: A Scoping Review. Bioengineering 2023, 10, 848. https://doi.org/10.3390/bioengineering10070848

AMA Style

Carlomagno V, Mirabella M, Lucchini M. Current Status of Oral Disease-Modifying Treatment Effects on Cognitive Outcomes in Multiple Sclerosis: A Scoping Review. Bioengineering. 2023; 10(7):848. https://doi.org/10.3390/bioengineering10070848

Chicago/Turabian Style

Carlomagno, Vincenzo, Massimiliano Mirabella, and Matteo Lucchini. 2023. "Current Status of Oral Disease-Modifying Treatment Effects on Cognitive Outcomes in Multiple Sclerosis: A Scoping Review" Bioengineering 10, no. 7: 848. https://doi.org/10.3390/bioengineering10070848

APA Style

Carlomagno, V., Mirabella, M., & Lucchini, M. (2023). Current Status of Oral Disease-Modifying Treatment Effects on Cognitive Outcomes in Multiple Sclerosis: A Scoping Review. Bioengineering, 10(7), 848. https://doi.org/10.3390/bioengineering10070848

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