Skip to main content
. 2021 Aug 16;55:103217. doi: 10.1016/j.msard.2021.103217

Table 3.

Disease-modifying treatment (DMT) as a risk factor for severe COVID-19 outcome in multiple sclerosis patients.a

Univariate analysis, (n=332) Multivariate analysis, (n=332)
DMT OR (95% CI) p value OR (95% CI) p value
Interferon 0.39 (0.17–0.81) 0.02 0.72 (0.34–1.40) 0.26
Glatiramer acetate 0.36 (0.14–0.79) 0.01 0.81 (0.42–1.83) 0.42
Teriflunomide 0.54 (0.29–1.17) 0.82 0.83 (0.39–1.97) 0.67
Fumaratesb 0.47 (0.17–0.79) 0.01 1.08 (0.49–2.09) 0.74
S1P modulatorsc 0.57 (0.21–0.96) 0.04 1.12 (0.52–2.34) 0.85
Natalizumab 0.42 (0.18–0.62) 0.01 1.18 (0.53–2.10) 0.76
Anti-CD20d 0.81 (0.63–1.23) 0.14 2.18 (1.53–4.58) 0.01
Other 0.41 (0.22–1.07) 0.07 1.24 (0.36–2.22) 0.80
No therapye 1 (ref) 1 (ref)

Abbreviations: CI, confidence interval; COVID-19, corona virus disease 2019; OR, odds ratio.

a

Intensive care unit admission, mechanical ventilation, and/or death.

b

Dimethyl fumarate, diroximel fumarate, or monomethyl fumarate.

c

Fingolimod, siponimod, or ozanimod.

d

Ocrelizumab or rituximab.

e

The no therapy group was used as the reference category.