Table 1.
MS | Control | p | |
---|---|---|---|
n = 17 | n = 17 | ||
Gender; n (%) | |||
Female | 11 (64.7) | 11 (64.7) | – |
Male | 6(35.3) | 6 (35.3) | |
Age, years; Mean ± SD; median (min–max) |
38.82 ± 7.68; 40 (23–51) |
38.91 ± 7.62; 40 (23–51) |
0.782* |
MS disease type; n (%) | |||
RRMS | 13 (76.5) | ||
SPMS | 4 (23.5) | ||
MS disease duration, years Mean ± SD; median(min–max) |
9.9 ± 5.8;10 (2–22) | – | |
ARR | 0.59 ± 0.45; 0.53 (0.10–2) | – | |
EDSS Mean ± SD; median (min–max) |
2.35 ± 1.22; 2 (1–4.5) | – | |
In treatment, n (%) | |||
Glatiramer acetate | 2 (11.8) | – | |
Interferon beta | 1 (5.9) | – | |
Teriflunamide | 3 (17.6) | – | |
Dimethyl fumarate | 2 (11.8) | – | |
Fingolimod | 2 (11.8) | – | |
Natalizumab | 1 (5.9) | – | |
Ocrelizumab | 4 (23.5) | – | |
Rituksimab | 2 (11.8) | – | |
Treatment duration, months Mean ± SD; median (min–max) |
40.35 ± 32.60; 31 (6–119) |
– | – |
COVID-19 severity | – | ||
Mild | 12 (70.16) | 12 (70.16) | |
Moderate | 3 (17.6) | 3 (17.6) | |
Severe | 2 (11.8) | 2 (11.8) | |
Time between COVID-19 symptom onset and SARS-CoV-2 antibody testing, days Mean ± SD; median (min–max) |
79.65 ± 49.94; 65 (14–160) |
64.76 ± 47.74; 45 (22–162) |
0.397* |
Antibody response distribution n (%) | |||
IgM Antibody positive | 9 (52.9) | 14 (82.4) | 0.06** |
IgM Antibody negative | 8 (47.1) | 3 (17.6) | |
IgG Antibody positive | 9 (52.9) | 15 (88.2) | 0.02** |
IgG Antibody negative | 8 (47.1) | 2 (11.8) | |
IgM antibody titer Mean ± SD; median (min–max) |
3.11 ± 3.53; 1.56 (0–10.31) |
3.28 ± 2.83; 2.36 (0.02–9.06) |
0.642* |
IgG Antibody titer Mean ± SD; median (min–max) |
2.65 ± 3.11; 1.15 (0–11.14) |
4.76 ± 3.23; 4.17 (0.19–10.66) |
0.052* |
RRMS relapsing remitting multiple sclerosis, SPMS secondary progressive multiple sclerosis, ARR annual relapse rate
*Mann–Whitney U test
**Chi-square test