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. 2024 Nov 12;15:1480676. doi: 10.3389/fimmu.2024.1480676

Table 1.

Baseline data and patient characteristics.

Variable All patients (n = 115)
Age (years)
Median [range]
39.8 [22.1–65.6]
BMI
Median [range]
23.0 [15.4–37.9]
Sex (F/M) 76/39
Current smoker N (%) 12 (10.4%)
Disease duration (years)
Median [range]
6.4 [0.1–30.8]
EDSS score
Median [range]
2.0 [1.0–6.5]
sNfL
Median [range]
7.9 [1.6–382.9]
z-score sNfL
Median [range]
0.4 [−3.4–4.0]
sGFAP
Median [range]
139.3 [48.6–1,285.1]
Card. Comorbidities N (%)
High blood pressure
Cardiomyopathy
Ischemic heart disease
7 (6.1%)
1 (0.9%)
0 (0.0%)
Previous treatment N (%)
Naïve
Platform
Orals
Monoclonal Ab
27 (23.5%)
27 (23.5%)
43 (37.4%)
18 (15.6%)
Reason for switching previous treatment N (%)
Effectiveness
Safety
78 (88.6%)
10 (11.4%)
T2 lesions on MRI N (%).
<10 lesions
10–50 lesions
50–100 lesions
>100 lesions
12 (10.4%)
77 (67.0%)
23 (20.0%)
3 (2.6%)
Gd lesions on MRI N -%).
At least one lesion 49 (42.6%)

BMI, body mass index; F, female; M, male; Card, cardiovascular; EDSS, Expanded Disability Status Scale; sNfL, serum neurofilament light chains; sGFAP, serum glial fibrillary acidic protein; n, number of patients; Ab, antibody; Naïve, no previous treatment; Gd: gadolinium-enhancing lesions.

Platform treatments included interferon beta and glatiramer acetate. Oral drugs included cladribine, dimethylfumarate, fingolimod, and teriflunomide. Monoclonal Ab. included alemtuzumab and natalizumab.