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. 2015 Feb 4;132(2):111–117. doi: 10.1111/ane.12363

Table 1.

Demographic and clinical characteristics of study patients

Patients with multiple sclerosis (n = 156)
Male, n (%) 45 (28.8)
Female, n (%) 111 (71.2)
Age, years, mean ± SE
At study entry 36.95 ± 0.92
At disease onset 31.97 ± 0.80
At diagnosis 36.48 ± 0.89
At follow‐up (end of the study) 39.55 ± 0.91
Clinical form at study entry, n (%)
Relapsing remitting 115 (73.7)
Primary progressive 17 (10.9)
Secondary progressive 24 (15.4)
Pregnancy, n/N (%)a 13/111 (11.7)
Treatment during the follow‐up period, n/N (%)b 99/156 (63.5)
Interferon beta 67/156 (42.9)
Glatiramer acetate 20/156 (12.8)
Selective immunosuppressants (natalizumab and fingolimod) 10/156 (6.4)
Untreated at study endc 57/156 (36.5)
EDSS, mean ± SE (N = 154)d 3.61 ± 0.19
EDSS <4, n/N (%)d 88/154 (57.1)
EDSS ≥4, n/N (%)d 66/154 (42.9)
Years of monitoring, mean ± SE, N = 154d 7.55 ± 0.44
Number of visits, mean ± SE, N = 154d 11.44 ± 0.73
Visits per year, mean ± SE, N = 154d 2.23 ± 0.17

EDSS, Expanded Disability Status Scale; SE, standard error.

a

Cumulative incidence of pregnancies over the 20‐year study period in 111 women.

b

Treatment data were collected at the final study visit (31 December 2011).

c

Untreated patients were those with benign forms of the disease who did not meet the criteria for disease‐modifying treatments.

d

Two patients were excluded from the analysis of disability because data were not available for these patients.