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. Author manuscript; available in PMC: 2017 Apr 15.
Published in final edited form as: J Neurol Sci. 2016 Feb 20;363:153–157. doi: 10.1016/j.jns.2016.02.042

Table 1. Baseline characteristics of the pediatric multiple sclerosis (MS) casesϕ.

Characteristic, n (%) unless stated otherwise MS cases, n=17
Sex: Girl 10 (59%)
Boy 7 (41%)
Age, years: mean (SD; range) 12.5 years
(SD=4.57; 4-17)
Age: ≤12 years old 5 (29%)
>12 years old 12 (61%)
Race: White 8 (47%)
Non-white 9 (53%)
Ethnicity: Hispanic 8 (47%)
Non- Hispanic 9 (53%)
Co-morbid condition [a]: present 7 (41%)
Absent 10 (59%)
MS-Specific clinical characteristics
Age at MS symptom onset, years: mean (SD; range) 12.1 years (SD=4.8; 4-17)
Disease duration [b], months: mean (SD; range) 10.3 months
(SD=6.6; 2.3-23.1)
Time since last relapse or onset attack (onset attack considered):
days: mean (SD; range)
183 days (SD=140; 4 to
489 days)
Disability level - EDSS at enrolment, median (range) 2.0 (0-4.0)
0-<2.0 7
2.0-<3.0 7
3.0+ 3
Immunomodulatory drug exposure status [c]: IMD nai̇ve 8 (47%)
IMD exposed 9 (53%)
Corticosteroids – systemic [d]: No 11 (65%)
Yes 6 (35%)
Available prospective follow-up, months: mean (SD; range) 19.8 months
(SD=12.0; 1.8-41.6)

Key: SD=standard deviation; EDSS=Expanded Disability Status Scale score; IMD=immunomodulatory drug

ϕ

data shown are in relation to baseline (i.e. date of stool sample collection) unless otherwise stated. EDSS was assessed at the clinic visit nearest to the stool sample, i.e. at enrollment into the study

all prospective follow-up was expressed regardless if (or when) a relapse occurred, with the study end being the last clinic visit or contact for each child

[a]

the comorbid conditions for the 7 children were: headache, atopic dermatitis/eczema, long-term constipation, history of shingles, seizures, reactive airways disease and headache, scoliosis

[b]

disease duration: time from symptom onset to baseline (stool collection)

[c]

‘IMD naïve’ indicates never exposed pre-baseline. ‘IMD exposed’ indicates ever exposed pre-baseline. At baseline, all IMD exposed cases were still on an MS drug as follows: beta-interferon (n=3); glatiramer acetate (n=5); natalizumab (n=1). No child had switched or stopped an IMD (although one child had previously been exposed to plasma exchange before taking glatiramer acetate).

[d]

within the previous 2 months