Table 3

Linear regression for annualised SC atrophy rate over 24 months, adjusted for centre

UnivariateMultivariate
Coefficient bSEp ValueCoefficient bSEp Value
Clinical parameters
 Centre* (A vs B)0.670.280.020.410.280.14
 Gender (male vs female)−0.350.290.23
 MS subtype (RR=1; PP and SP=0)*0.850.31<0.010.590.340.08
 Age*−0.010.010.51
 Disease duration*−0.030.020.04−0.060.020.003
 Use of DMT*−0.040.280.89
 EDSS baseline−0.110.090.23
MRI parameters
 NGMV baseline*0.0040.0020.09
 NWMV baseline−0.0040.0030.16
 NBV baseline0.0010.0020.73
 T2LV baseline† *−0.140.090.13
 T1LV baseline†−0.080.070.23
 Presence of Gd+ brain lesions at baseline0.030.390.94
 Number of SC segments† *−0.440.190.03−0.490.190.01
 Number of SC lesions†−0.330.180.08
 UCCA baseline*−0.040.010.002−0.060.02<0.001
 Diffuse SC abnormalities baseline (0=absent; 1=present)*−0.520.440.23−0.960.420.02
 Δ T2 LV (0–24 month)†0.690.440.12
 aPBVC (0–24 month)*0.560.240.02
 Δ T1 LV (0–24 month)† *−1.290.660.05−1.40.70.04
  • Models were statistically adjusted for centre. The model accounts for 238 patients with MS (68%) with all parameters available. R2 of the model was 0.14.

  • *Independent variables that were initially entered in the multivariate model.

  • †Data were obtained with natural log transformation.

  • aPBVC, annualised percentage brain volume change; Centre A, Amsterdam, Centre B, Basel; DMT, disease modifying therapy; EDSS, expanded disability status scale; Gd+: gadolinium enhancing; MS, multiple sclerosis; NBV: brain volume normalised for head size; NGMV, normalised grey matter volume; NWMV: normalised white matter volume; PPMS: primary progressive MS; RRMS, relapsing remitting MS; SC: spinal cord; SPMS: secondary progressive MS; T2LV: volume of T2 brain lesion; T1LV: volume of T1 hypointense brain lesion; UCCA: mean upper cervical cord cross-sectional area.