Details

Autor(en) / Beteiligte

• Yalachkov, Yavor
• Anschütz, Victoria
• Maiworm, Michelle
• Jakob, Jasmin
• Schaller-Paule, Martin A.
• Schäfer, Jan Hendrik
• Reiländer, Annemarie
• Friedauer, Lucie
• Behrens, Marion
• Steffen, Falk
• Bittner, Stefan
• Foerch, Christian

Titel

Serum and cerebrospinal fluid BDNF concentrations are associated with neurological and cognitive improvement in multiple sclerosis: A pilot study

Ist Teil von

• Multiple sclerosis and related disorders, 2023-03, Vol.71, p.104567-104567, Article 104567

Ort / Verlag

Netherlands: Elsevier B.V

Erscheinungsjahr

2023

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• •Brain-derived neurotrophic factor concentrations in serum and CSF (sBDNF/cBDNF).•RRMS, PPMS and CIS patients at baseline and 12 months follow-up.•EDSS improvement was associated with higher sBDNF at baseline.•Cognitive improvement was associated with higher cBDNF at baseline.•Possible role for BDNF in neurological and cognitive improvement in MS. Biomarkers of disease activity have been intensively studied in multiple sclerosis (MS) but knowledge on predictors of disability improvement is limited. The aim of this pilot study was to explore whether increased brain-derived neurotrophic factor concentrations in serum and CSF (sBDNF/cBDNF) precede neurological and cognitive improvement in MS. In this pilot, monocentric prospective cohort study we collected serum/CSF samples at baseline together with EDSS (n = 36) and cognitive testing (n = 34) in patients with relapsing-remitting/primary progressive MS or clinically isolated syndrome. BDNF was assessed in serum and CSF with a single molecule array (SIMOA) HD-1 analyser (Quanterix). Twelve months later EDSS and cognitive testing were repeated. BDNF concentrations of patients with vs. without disability or cognitive improvement (disability improvement: decrease in EDSS ≥ 0.5; cognitive improvement: average z-score increase in neuropsychological performance ≥ 0.5) were compared using univariate ANOVAs adjusting for covariates. Compared to subjects without, patients with disability improvement had higher sBDNF at baseline (q = 0.04). Subjects with cognitive improvement had higher cBDNF at baseline than those without cognitive improvement (q = 0.004). Secondary analysis demonstrated significant correlations between sBDNF and EDSS change (q = 0.036), cBDNF and average z-score change (q = 0.04) and cBDNF and number of cognitive tests with improvement (q = 0.04), while controlling for covariates. Our findings suggest a possible role for BDNF in neurological and cognitive improvement in MS. These findings have to be confirmed in a larger sample but they already highlight the potential of BDNF as a biomarker for disability improvement and neuroplasticity in MS.