Exploring the Prognostic Role of Neurofilaments and SEMA3A in Multiple Sclerosis Progression
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, pozorovací studie
Grantová podpora
NA
Charles University, Czech Republic (Cooperatio Program, research area NEUR),
DRO-UHHK 00179906
the Ministry of Health of the Czech Republic
PubMed
40943667
PubMed Central
PMC12429374
DOI
10.3390/ijms26178750
PII: ijms26178750
Knihovny.cz E-zdroje
- Klíčová slova
- functional capacity, immunity, multiple sclerosis, neuroimmunology,
- MeSH
- biologické markery krev MeSH
- chronicko-progresivní roztroušená skleróza * krev diagnóza MeSH
- dospělí MeSH
- interleukin-6 krev MeSH
- intermediární filamenta * metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- neurofilamentové proteiny * krev MeSH
- prognóza MeSH
- progranuliny krev MeSH
- progrese nemoci MeSH
- relabující-remitující roztroušená skleróza * krev diagnóza MeSH
- semaforin-3a * krev MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
- Názvy látek
- biologické markery MeSH
- interleukin-6 MeSH
- neurofilamentové proteiny * MeSH
- progranuliny MeSH
- SEMA3A protein, human MeSH Prohlížeč
- semaforin-3a * MeSH
The transition from relapsing-remitting multiple sclerosis (RRMS) to secondary progressive multiple sclerosis (SPMS) is characterized by an increasing neurodegenerative component. Identifying biomarkers that distinguish these disease stages is crucial for early diagnosis and treatment optimization. This study aimed to compare serum levels of progranulin, interleukin-6 (IL-6), semaphorin 3A (SEMA3A), and neurofilaments between RRMS and SPMS patients and to investigate their correlation with clinical characteristics, including disability measured by the Expanded Disability Status Scale (EDSS). This observational study included 118 MS patients (63 RRMS and 55 SPMS). Serum biomarker levels were measured using an enzyme-linked immunosorbent assay (ELISA). Statistical analyses included group comparisons using non-parametric tests and correlation analyses using Pearson's correlation coefficient with multiple testing corrections. While demographic and clinical parameters significantly differed between groups (p < 0.001), biomarker levels showed no statistically significant differences (p > 0.05). However, in SPMS patients, SEMA3A correlated positively with neurofilaments (r = 0.359, p = 0.007), and progranulin correlated with IL-6 (r = 0.354, p = 0.008). No significant biomarker correlations with EDSS were found. Although absolute biomarker levels did not distinguish RRMS from SPMS, specific biomarker correlations may reflect processes relevant to disease progression and warrant further longitudinal validation.
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