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. 2022 Mar 2;269(5):2286–2292. doi: 10.1007/s00415-022-11030-0

Table 1.

Demographic, clinical, and COVID-19 third vaccine dose immune-related variables

Study population MS patients
N = 20
Group 1 fingolimod-continuation N = 10 Group 2 fingolimod-discontinuation N = 10 p
Gender, n (%)
 Females 8 (80.0) 4 (40.0)
 Males 2 (20.0) 6 (60.0)
Age, years
 Median 51.6 47.5 0.69
 25–75 IQR 46.9–58.1 43.0–54.9
Disease duration, years
 Median 20.9 15.9 0.10
 25–75 IQR 18.3–23.5 6.5–18.9
Disability by EDSS
 Median 2.25 2.0 0.89
 25–75 IQR 1.1–2.9 1.5–3.6
Fingolimod Tx duration, years
 Median 7.25 4.8 0.15
 25–75 IQR 5.6–8.3 2.5 -8.4
Time from 2nd to 3rd vaccine dose, months
 Median 6.6 6.2
 25–75 IQR 6.4–7.5 6.1–6.2 NS
Time without fingolimod treatment, months
 Median 4.2
 25–75 IQR 2.5–4.4
ALC at 3rd vaccine dose cells/mm3
 Median 775 1510  < 0.0001
 25–75 IQR 572–817 1190–1668

Patients with positive SARS-COV-2 IgG, 1 month

N, (%)

2 (20) 8 (80)
SARS-COV-2 IgG titer, BAU/ml, 1 month
 Median 26.4 202.3 0.022
 25–75 IQR 3.5–29.7 49.3–580.4

Patients with positive SARS-COV-19 IgG, 3 months

N, (%)

2 (20) 6 (60)
SARS-COV-2 IgG titer, BAU/ml, 3 months
 Median 12.1 115 0.0296
 25–75 IQR 4.8–18.4 23.3–269.8
% SARS-COV-2 IgG decay within 3 months 46.2 34.9