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. Author manuscript; available in PMC: 2021 Sep 4.
Published in final edited form as: Mult Scler. 2020 Dec 14;27(10):1506–1519. doi: 10.1177/1352458520971816

Table 6.

Demographic characteristics of the longitudinal EDSS-lipidomics cohort

Characteristic Whole cohort (n=185) Stable group (n=115) Group with disability progression (n=70) p value (stable vs. progressing)
Age (years), mean (SD) 44.8 (11.8) 44.0 (11.9) 46.1 (11.6) 0.25a

Female Sex, n (%) 135 (73%) 93 (81%) 42 (60%) 0.002 b

Race, n (%) 0.036 c
Caucasian American 152 (82%) 96 (83%) 56 (80%)
African American 23 (12%) 10 (9%) 13 (19%)
Other 10 (5%) 9 (8%) 1 (1%)

MS subtype, n (%) <0.001 b
RRMS 118 (64%) 90 (78%) 28 (40%)
PMS 67 (36%) 25 (22%) 42 (60%)

DMT at baseline d
None 27 (15%) 13 (11%) 14 (20%)
High potency 67 (36%) 39 (34%) 28 (40%)
Intermediate potency 6 (3%) 3 (3%) 3 (4%)
Low potency 79 (43%) 56 (49%) 23 (33%)
Other 6 (3%) 4 (3%) 2 (3%)

EDSS at baseline, median (IQR) 3 (2-6) 2.5 (1.5-5) 3.5 (2-6) 0.11e

Disease duration (years), median (IQR) 9 (6-15) 9 (6-14) 10 (6-17) 0.24e

Follow-up (years), median (IQR) 5.0 (4.6-5.3) 5.0 (4.6-5.3) 4.9 (4.7-5.3) 0.54e
a

Student’s t-test

b

Chi-square test

c

Fisher’s exact test

d

Glatiramer acetate, interferon-beta, and teriflunomide were classified as low-potency DMTs, dimethyl fumarate and fingolimod as intermediate-potency DMTs, and natalizumab, ocrelizumab, rituximab, alemtuzumab, and daclizumab as high-potency DMTs.

e

Wilcoxon rank-sum test

MS: Multiple Sclerosis; RRMS: Relapsing-Remitting MS; PMS: Progressive MS; SD: Standard Deviation; DMT: Disease Modifying Treatment; EDSS: Expanded Disability Status Scale; IQR: Interquartile range