Number of patients |
554 |
|
Age (years) |
46.7 (11.6) |
|
Sex (F/M) |
395/158 |
71%/29% |
MS phenotype |
|
|
|
RRMS |
340 |
61.4% |
|
SPMS |
152 |
27.4% |
|
PPMS |
62 |
11.2% |
Disease duration (years) |
|
|
|
since onset |
12.5 (10.1) |
|
|
|
#9.7 (4.2–18.8) |
|
|
since diagnosis |
7.2 (7.7) |
|
|
|
#4.2 (0.9–11.3) |
|
Age (years) |
|
|
|
at onset |
34.2 (10.4) |
|
|
at diagnosis |
39.6 (10.8) |
|
Number of pre baseline relapses (in 3 years) |
|
|
|
0 |
196 |
35.4% |
|
1 |
147 |
26.5% |
|
2 |
104 |
18.8% |
|
3 or more |
107 |
19.3% |
Baseline EDSS |
4.0 (2.0–6.0) |
|
|
≤3.5 |
274 |
49.5% |
|
4.0–5.5 |
129 |
23.2% |
|
≥6.0 |
151 |
27.3% |
EDSS after 3 years follow-up |
4.0 (2.5–6.5) |
|
|
≤3.5 |
228 |
41.2% |
|
4.0–5.5 |
140 |
25.3% |
|
≥6.0 |
186 |
33.6% |
Number of patients with EDSS progression after 3 years follow-up |
|
|
|
<1 |
357 |
64.4% |
|
≥1 |
197 |
35.6% |
Baseline 25(OH)D (nmol/L) |
|
|
|
crude |
57.5 (28.4) |
|
|
deseasonalized |
56.7 (28.0) |
|
Disease modifying treatment used most frequently during follow-up |
|
|
|
none |
225 |
40.6% |
|
first line treatment (interferon, glatiramer acetate) |
193 |
34.8% |
|
second line treatment (natalizumab, fingolimod) |
40 |
7.2% |
|
third line treatment (methotrexate, immunoglobulins, mitoxantrone) |
75 |
13.5% |
|
Other |
6 |
1.0% |
|
Unknown |
15 |
2.7% |
Number of relapses during three year follow-up |
|
|
|
0 |
288 |
52.0% |
|
1 |
130 |
23.5% |
|
2 |
67 |
12.1% |
|
3 or more |
69 |
12.5% |