Elevated serum neurofilament light chain levels in patients with neuropsychiatric systemic lupus erythematosus: a cross-sectional study
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
PubMed
39832906
PubMed Central
PMC11752028
DOI
10.1136/lupus-2024-001309
PII: 12/1/e001309
Knihovny.cz E-zdroje
- Klíčová slova
- autoimmune diseases, cytokines, systemic lupus erythematosus,
- MeSH
- biologické markery * krev mozkomíšní mok MeSH
- dospělí MeSH
- ELISA MeSH
- interleukin-6 krev mozkomíšní mok MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- neurofilamentové proteiny * krev mozkomíšní mok MeSH
- průřezové studie MeSH
- studie případů a kontrol MeSH
- vaskulitida centrálního nervového systému při lupus erythematodes * krev mozkomíšní mok MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- biologické markery * MeSH
- interleukin-6 MeSH
- neurofilament protein L MeSH Prohlížeč
- neurofilamentové proteiny * MeSH
BACKGROUND: The neurofilament light chain (NfL) in cerebrospinal fluid (CSF) and serum as a marker of neuronal damage may be a potential biomarker of neuropsychiatric involvement in SLE (NPSLE). METHODS: 80 patients with SLE were included.We obtained paired serum and CSF samples from 48 patients (NPSLE n=32, non-NPSLE n=16) and 31 controls. The serum and CSF levels of NfL were determined using ELISA. RESULTS: Patients with NPSLE demonstrated significantly higher levels of serum NfL compared with the non-NPSLE group (mean 31.68±36.63 pg/mL vs mean 16.75±12.48 pg/mL, respectively, p<0.05) and with controls (mean 10.74±4.36 pg/mL, p<0.01). Notably, CSF NfL concentrations in patients with NPSLE showed an upward trend (mean 1600±2852 pg/mL) in contrast to non-NPSLE patients (mean 393.4±191.9 pg/mL) and controls (mean 509.7±358.5 pg/mL). Furthermore, a positive correlation was observed between serum and CSF NfL levels in patients with NPSLE (R=0.8686, p<0.01). Elevated serum triacylglycerol concentrations, C reactive protein and organ damage were linked to increased serum (p=0.002; p<0.001; p=0.036) and CSF (p=0.008; p=0.007; p<0.001) NfL concentrations. In addition, we established a significant correlation between intrathecal NfL concentrations and interleukin-6 levels in the CSF of patients with NPSLE (R=0.5118, p<0.05). CONCLUSION: The serum NfL levels may be a readily available marker of neuropsychiatric involvement in SLE.
Department of Neurology Charles University Prague Czech Republic
Department of Rheumatology Charles University Praha Czech Republic
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