Staging of relapsing-remitting multiple sclerosis - the promising role of the BDNF/VEGF ratio
Introduction/Objective. Brain-derived neurotrophic factor (BDNF) and vascular endothelial growth factor (VEGF) may play important roles in the development and monitoring of multiple sclerosis (MS). BDNF is a neuroprotective factor in the process of inflammation, degeneration, and demyelination in MS. Inflammatory cells stimulate angiogenesis in demyelinating lesions through the release of VEGF, which is a proinflammatory factor. Methods. The study included 86 subjects: 20 healthy individuals and 66 patients with relapsing, who were divided into three groups: patients in remission, patients at the onset of MS relapse, and patients at the end of corticosteroid therapy for disease relapse. Results. The study showed a statistically significant difference in BDNF concentration between patient groups at baseline and at the end of therapy for disease relapse, as well as a difference in VEGF concentration between groups. The BDNF/VEGF ratio was increased in patients in remission compared with the control group; this ratio decreased significantly in patients at the onset of MS relapse compared with patients in remission. Conclusion. This study describes the BDNF/VEGF ratio for the first time as a biomarker that may be of interest in well-controlled longitudinal studies for staging relapsing?remitting multiple sclerosis and evaluating the response to therapy during relapses.
Authors
- Aleksandra Stajić
- Tamara Andjelic
- Milica Ninković (ORCID: https://orcid.org/0000-0003-3303-9916)
- Miloš Todorović (ORCID: https://orcid.org/0000-0002-6166-7103)
- Ivana Stevanović (ORCID: https://orcid.org/0000-0002-4588-3447)
- Adam Nikic
- Kosta Karanovic
Institutions
- Military Medical Academy (RS)
- University of Defence (RS)
Publication Details
- Journal
- Srpski arhiv za celokupno lekarstvo
- Published
- 2025-12-23
- DOI
- https://doi.org/10.2298/sarh241204096s
- Primary Topic
- Multiple Sclerosis Research Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00