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. 2023 May 24;5(3):fcad153. doi: 10.1093/braincomms/fcad153

Table 1.

Baseline demographics and clinical characteristics of included participants

Healthy volunteers (N = 37) People with MS (N = 41) Group differencesa
P-value*
Demographics
Age, years 39.3 (14.3) 45.2 (12.9) 0.052
Sex, male/female [number (%)] 16 (43.2) / 21 (56.8) 11 (26.8) / 30 (73.2) 0.128
Education, years 16.2 (2.5)
Disease characteristics
Disease duration, years 9.7 (6.9)
MS subtype, RR/SP/PP 33 (80.5)/5 (12.2)/3 (7.3)
DMT use,b yes [number (%)] 35 (85.4)
Clinical characteristics
EDSS, score 2.5 [2.0–3.5]
SDMT, raw score 51.0 (12.5)
MR characteristics
WM lesion load, mL 4.13 [1.87–10.80]
Cortical GM volume, mL 478.9 (57.8) 421.0 (73.9) 2.68 × 10−4
Normalized cortical GM volume, mL 0.30 (0.02) 0.27 (0.03) 6.39 × 10−9
Deep GM volume, mL 44.4 (4.0) 41.9 (5.0) 0.016
Normalized deep GM volume, mL 0.028 (0.002) 0.027 (0.002) 2.82 × 10−4

Variables are reported as mean (SD) or median (IQR) unless otherwise indicated. DMT, disease-modifying treatment; EDSS, Expanded Disability Status Scale; GM, grey matter; PP, primary progressive; MR, magnetic resonance; MS, multiple sclerosis; RR, relapsing-remitting; SDMT, Symbol Digit Modalities Test; SP, secondary progressive; WM, white matter. aIndependent samples t-test. bSpecific disease-modifying therapies include: nine dimethyl fumarate, eight glatiramer acetate, five fingolimod, five ocrelizumab, three interferon beta (1a/1b), two natalizumab, two rituximab and one teriflunomide. *P-values <0.05 are marked in bold.