A Multi-Centre Longitudinal Study Analysing Multiple Sclerosis Disease-Modifying Therapy Prescribing Patterns During the Covid-19 Pandemic

Loading...
Publication Logo

Date

2024

Journal Title

Journal ISSN

Volume Title

Publisher

Springer heidelberg

Open Access Color

HYBRID

Green Open Access

Yes

OpenAIRE Downloads

OpenAIRE Views

Publicly Funded

No
Impulse
Top 10%
Influence
Average
Popularity
Top 10%

Research Projects

Journal Issue

Abstract

BackgroundThe COVID-19 pandemic raised concern amongst clinicians that disease-modifying therapies (DMT), particularly anti-CD20 monoclonal antibodies (mAb) and fingolimod, could worsen COVID-19 in people with multiple sclerosis (pwMS). This study aimed to examine DMT prescribing trends pre- and post-pandemic onset.MethodsA multi-centre longitudinal study with 8,771 participants from MSBase was conducted. Two time periods were defined: pre-pandemic (March 11 2018-March 10 2020) and post-pandemic onset (March 11 2020-11 March 2022). The association between time and prescribing trends was analysed using multivariable mixed-effects logistic regression. DMT initiation refers to first initiation of any DMT, whilst DMT switches indicate changing regimen within 6 months of last use.ResultsPost-pandemic onset, there was a significant increase in DMT initiation/switching to natalizumab and cladribine [(Natalizumab-initiation: OR 1.72, 95% CI 1.39-2.13; switching: OR 1.66, 95% CI 1.40-1.98), (Cladribine-initiation: OR 1.43, 95% CI 1.09-1.87; switching: OR 1.67, 95% CI 1.41-1.98)]. Anti-CD20mAb initiation/switching decreased in the year of the pandemic, but recovered in the second year, such that overall odds increased slightly post-pandemic (initiation: OR 1.26, 95% CI 1.06-1.49; Switching: OR 1.15, 95% CI 1.02-1.29. Initiation/switching of fingolimod, interferon-beta, and alemtuzumab significantly decreased [(Fingolimod-initiation: OR 0.55, 95% CI 0.41-0.73; switching: OR 0.49, 95% CI 0.41-0.58), (Interferon-gamma-initiation: OR 0.48, 95% CI 0.41-0.57; switching: OR 0.78, 95% CI 0.62-0.99), (Alemtuzumab-initiation: OR 0.27, 95% CI 0.15-0.48; switching: OR 0.27, 95% CI 0.17-0.44)].ConclusionsPost-pandemic onset, clinicians preferentially prescribed natalizumab and cladribine over anti-CD20 mAbs and fingolimod, likely to preserve efficacy but reduce perceived immunosuppressive risks. This could have implications for disease progression in pwMS. Our findings highlight the significance of equitable DMT access globally, and the importance of evidence-based decision-making in global health challenges.

Description

Keywords

Multiple sclerosis, COVID-19, Disease-modifying therapy, Anti-CD20 monoclonal antibodies, Cladribine, Natalizumab, Male, Adult, Multiple Sclerosis, Immunologic Factors / therapeutic use, 610, cladribine, multiple sclerosis, COVID-19 / epidemiology, Multiple sclerosis, natalizumab, Fingolimod Hydrochloride / therapeutic use, Medicine and Health Sciences, Practice Patterns, Physicians' / statistics & numerical data, Disease-modifying therapy, Humans, Immunologic Factors, Longitudinal Studies, Practice Patterns, Physicians', Alemtuzumab, Original Communication, Fingolimod Hydrochloride, Anti-CD20 monoclonal antibodies, Natalizumab, COVID-19, Multiple Sclerosis / epidemiology, Middle Aged, anti-CD20 monoclonal antibodies, Alemtuzumab / therapeutic use, disease-modifying therapy, Natalizumab / therapeutic use, Anti-CD20 monoclonal antibodies; COVID-19; Cladribine; Disease-modifying therapy; Multiple sclerosis; Natalizumab, Cladribine / therapeutic use, Multiple Sclerosis / drug therapy, Cladribine, Female, Immunosuppressive Agents / therapeutic use, Immunosuppressive Agents, Clinical Medical Sciences, Biomedicine and Health Sciences, neurologija, Kliničke medicinske znanosti, Neurology, Biomedicina i zdravstvo

Fields of Science

03 medical and health sciences, 0302 clinical medicine

Citation

WoS Q

Q1

Scopus Q

Q1
OpenCitations Logo
OpenCitations Citation Count
N/A

Source

Journal of Neurology

Volume

271

Issue

Start Page

5813

End Page

5824
PlumX Metrics
Citations

Scopus : 6

PubMed : 5

Captures

Mendeley Readers : 9

Google Scholar Logo
Google Scholar™
OpenAlex Logo
OpenAlex FWCI
3.9312

Sustainable Development Goals