Risk of Getting COVID-19 in People With Multiple Sclerosis

Background and Objectives Several studies have assessed risk factors associated with the severity of COVID-19 outcomes in people with multiple sclerosis (PwMS). The potential role of disease-modifying therapies (DMTs) and demographic and clinical factors on the risk of acquiring SARS-CoV-2 infection has not been evaluated so far. The objective of this study was to assess risk factors of contracting SARS-CoV-2 infection in PwMS by using data collected in the Italian MS Register (IMSR). Methods A case-control (1:2) study was set up. Cases included PwMS with a confirmed diagnosis of COVID-19, and controls included PwMS without a confirmed diagnosis of COVID-19. Both groups were propensity score–matched by the date of COVID-19 diagnosis, the date of last visit, and the region of residence. No healthy controls were included in this study. COVID-19 risk was estimated by multivariable logistic regression models including demographic and clinical covariates. The impact of DMTs was assessed in 3 independent logistic regression models including one of the following covariates: last administered DMT, previous DMT sequences, or the place where the last treatment was administered. Results A total of 779 PwMS with confirmed COVID-19 (cases) were matched to 1,558 PwMS without COVID-19 (controls). In all 3 models, comorbidities, female sex, and a younger age were significantly associated (p < 0.02) with a higher risk of contracting COVID-19. Patients receiving natalizumab as last DMT (OR [95% CI]: 2.38 [1.66–3.42], p < 0.0001) and those who underwent an escalation treatment strategy (1.57 [1.16–2.13], p = 0.003) were at significantly higher COVID-19 risk. Moreover, PwMS receiving their last DMT requiring hospital access (1.65 [1.34–2.04], p < 0.0001) showed a significant higher risk than those taking self-administered DMTs at home. Discussion This case-control study embedded in the IMSR showed that PwMS at higher COVID-19 risk are younger, more frequently female individuals, and with comorbidities. Long-lasting escalation approach and last therapies that expose patients to the hospital environment seem to significantly increase the risk of SARS-CoV2 infection in PwMS. Classification of Evidence This study provides Class III evidence that among patients with MS, younger age, being female individuals, having more comorbidities, receiving natalizumab, undergoing an escalating treatment strategy, or receiving treatment at a hospital were associated with being infected with COVID-19. Among patients with MS who were infected with COVID-19, a severe course was associated with increasing age and having a progressive form of MS, whereas not being on treatment or receiving an interferon beta agent was protective.

[1]  M. Sormani,et al.  DMTs and Covid‐19 severity in MS: a pooled analysis from Italy and France , 2021, Annals of clinical and translational neurology.

[2]  C. Oreja-Guevara,et al.  Risk and outcomes of COVID‐19 in patients with multiple sclerosis , 2021, European journal of neurology.

[3]  E. Havrdová,et al.  Update on the management of multiple sclerosis during the COVID-19 pandemic and post pandemic: An international consensus statement , 2021, Journal of Neuroimmunology.

[4]  M. Trojano,et al.  A randomized study of natalizumab dosing regimens for relapsing–remitting multiple sclerosis , 2021, Multiple sclerosis.

[5]  P. Levy,et al.  Review of the COVID-19 Risk in Multiple Sclerosis , 2021, Journal of cellular immunology.

[6]  R. D. Du Pasquier,et al.  Recurrence of disease activity after fingolimod discontinuation in older patients previously stable on treatment. , 2021, Multiple sclerosis and related disorders.

[7]  G. Cutter,et al.  Outcomes and Risk Factors Associated With SARS-CoV-2 Infection in a North American Registry of Patients With Multiple Sclerosis , 2021, JAMA neurology.

[8]  D. Centonze,et al.  COVID-19 in Patients with Multiple Sclerosis: Associations with Disease-Modifying Therapies , 2021, CNS Drugs.

[9]  M. Sormani,et al.  Disease‐Modifying Therapies and Coronavirus Disease 2019 Severity in Multiple Sclerosis , 2021, Annals of neurology.

[10]  M. Raponi,et al.  The role of air conditioning in the diffusion of Sars-CoV-2 in indoor environments: A first computational fluid dynamic model, based on investigations performed at the Vatican State Children's hospital , 2020, Environmental Research.

[11]  Jana K Dickter,et al.  Nosocomial Infections: A History of Hospital-Acquired Infections. , 2020, Gastrointestinal endoscopy clinics of North America.

[12]  H. Hartung,et al.  Multiple sclerosis and COVID-19. , 2020, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

[13]  C. Louapre,et al.  Clinical Characteristics and Outcomes in Patients With Coronavirus Disease 2019 and Multiple Sclerosis. , 2020, JAMA neurology.

[14]  J. Lechner-Scott,et al.  The COVID-19 pandemic and the use of MS disease-modifying therapies , 2020, Multiple Sclerosis and Related Disorders.

[15]  Kai Zhao,et al.  A pneumonia outbreak associated with a new coronavirus of probable bat origin , 2020, Nature.

[16]  B. Sharrack,et al.  Lymphocyte pharmacodynamics are not associated with autoimmunity or efficacy after alemtuzumab , 2019, Neurology: Neuroimmunology & Neuroinflammation.

[17]  R. Kinkel,et al.  Post-natalizumab disease reactivation in multiple sclerosis: systematic review and meta-analysis , 2019, Therapeutic advances in neurological disorders.

[18]  Angelo Ghezzi,et al.  The Italian multiple sclerosis register , 2018, Neurological Sciences.

[19]  G. Pardo,et al.  The sequence of disease-modifying therapies in relapsing multiple sclerosis: safety and immunologic considerations , 2017, Journal of Neurology.

[20]  T. Plavina,et al.  A Randomized Trial Evaluating Various Administration Routes of Natalizumab in Multiple Sclerosis , 2016, Journal of clinical pharmacology.

[21]  F. Novelli,et al.  Alemtuzumab Long Term Immunological Study: The Immunosuppressive Effect Does Not Last More Than 48 Months , 2016 .

[22]  H. Hartung,et al.  Disease-modifying therapies and infectious risks in multiple sclerosis , 2016, Nature Reviews Neurology.

[23]  G. Giovannoni,et al.  Long term lymphocyte reconstitution after alemtuzumab treatment of multiple sclerosis , 2011, Journal of Neurology, Neurosurgery & Psychiatry.

[24]  Peter C Austin,et al.  A comparison of the ability of different propensity score models to balance measured variables between treated and untreated subjects: a Monte Carlo study , 2007, Statistics in medicine.

[25]  Elaine L. Zanutto,et al.  Estimating causal effects of public health education campaigns using propensity score methodology , 2005 .

[26]  Lori S. Parsons Reducing Bias in a Propensity Score Matched-Pair Sample Using Greedy Matching Techniques , 2001 .