IL-2, IL-6 and chitinase 3-like 2 might predict early relapse activity in multiple sclerosis
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
35759479
PubMed Central
PMC9236235
DOI
10.1371/journal.pone.0270607
PII: PONE-D-22-08909
Knihovny.cz E-zdroje
- MeSH
- biologické markery mozkomíšní mok MeSH
- chitinasy metabolismus MeSH
- chronická nemoc MeSH
- interleukin-2 metabolismus MeSH
- interleukin-6 metabolismus MeSH
- lidé MeSH
- recidiva MeSH
- roztroušená skleróza * mozkomíšní mok diagnóza farmakoterapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biologické markery MeSH
- CHI3L2 protein, human MeSH Prohlížeč
- chitinasy MeSH
- IL2 protein, human MeSH Prohlížeč
- IL6 protein, human MeSH Prohlížeč
- interleukin-2 MeSH
- interleukin-6 MeSH
BACKGROUND: The possibility to better predict the severity of the disease in a patient newly diagnosed with multiple sclerosis would allow the treatment strategy to be personalized and lead to better clinical outcomes. Prognostic biomarkers are highly needed. OBJECTIVE: To assess the prognostic value of intrathecal IgM synthesis, cerebrospinal fluid and serum IL-2, IL-6, IL-10, chitinase 3-like 2 and neurofilament heavy chains obtained early after the onset of the disease. METHODS: 58 patients after the first manifestation of multiple sclerosis were included. After the initial diagnostic assessment including serum and cerebrospinal fluid biomarkers, all patients initiated therapy with either glatiramer acetate, teriflunomide, or interferon beta. To assess the evolution of the disease, we followed the patients clinically and with MRI for two years. RESULTS: The IL-2:IL-6 ratio (both in cerebrospinal fluid) <0.48 (p = 0.0028), IL-2 in cerebrospinal fluid ≥1.23pg/ml (p = 0.026), and chitinase 3-like 2 in cerebrospinal fluid ≥7900pg/ml (p = 0.033), as well as baseline EDSS ≥1.5 (p = 0.0481) and age <22 (p = 0.0312), proved to be independent markers associated with shorter relapse free intervals. CONCLUSION: The IL-2:IL-6 ratio, IL-2, and chitinase 3-like 2 (all in cerebrospinal fluid) might be of value as prognostic biomarkers in early phases of multiple sclerosis.
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