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Table 2 Demographic and clinical characteristics of the cohort

From: Combination protein biomarkers predict multiple sclerosis diagnosis and outcomes

 

Non-multiple sclerosis (n = 80)

Multiple sclerosis (n = 77)

Age at sampling—years—mean (SD)

33.2 (10.2)

41.9 (12.4)

Gender—count (%)

Female 72 (90%)

Male 8 (10%)

Female 46 (60%)

Male 31 (40%)

Diagnosis—count

IIH 59

Primary headache 10

Sensory disturbance 3

FND 3

Epilepsy 2

SPS 1

Arthritis 1

Viral meningitis 1

RRMS 57

SPMS 10

PPMS 10

Baseline EDSS—median (range)

 

2.5 (1.0–7.5)

Follow-up duration—mean (SD)

–

7.9 (3.5) years

Disease modifying therapy (ever exposed)—count

–

Yes 46* (High efficacy 27)

No 31

Relapse(s) experienced during follow-up—count (%)

–

46+ (60%)

Reached EDSS 6—count (%)

–

23 (30%)

Oligoclonal bands in CSF

–

Unpaired 53 (69%)

Paired 9 (12%)

Negative 15 (19%)

  1. IIH idiopathic intracranial hypertension, FND functional neurological disorder, SPS stiff person syndrome, RRMS relapsing–remitting multiple sclerosis, S/PPMS secondary/primary progressive multiple sclerosis. High efficacy disease modifying therapy: monoclonal antibody or cladribine treatment; *Only 2 people with multiple sclerosis were exposed to disease modifying therapy at the time of sampling. + 36 experienced their relapse prior to commencing disease modifying therapy (prior to censor)