Osteopontin Is Associated with Multiple Sclerosis Relapses

Mario Stampanoni Bassi1, Fabio Buttari1, Luana Gilio1

  • 1IRCCS Neuromed, 86077 Pozzilli, Italy.

Biomedicines
|January 21, 2023
PubMed
Abstract

Insights

Osteopontin levels in cerebrospinal fluid (CSF) increase near multiple sclerosis (MS) relapses. Higher osteopontin correlates with pro-inflammatory markers and lower anti-inflammatory markers during acute MS.

Area of Science:

  • Neuroimmunology
  • Biochemistry
  • Extracellular Matrix Biology

Background:

  • Osteopontin, an extracellular matrix protein, is implicated in inflammation and neurodegeneration in multiple sclerosis (MS).
  • Previous research links osteopontin to a worse disease course and potential involvement in acute MS relapses.

Purpose of the Study:

  • To investigate the relationship between osteopontin levels in cerebrospinal fluid (CSF) and the timing of clinical relapses in MS patients.
  • To explore correlations between CSF osteopontin, inflammatory cytokines, and adipokines in relapsing-remitting MS.

Main Methods:

  • Analysis of CSF from 47 patients with relapsing-remitting MS.
  • Measurement of osteopontin, inflammatory cytokines (IL-2, IL-6, IL-1β, IL-1ra), and adipokines (resistin, PAI-1, osteoprotegerin).
  • Correlation analysis between CSF molecule levels and time elapsed since the last clinical relapse.

Main Results:

  • Osteopontin CSF concentrations were elevated in patients with shorter intervals since their last clinical relapse.
  • CSF osteopontin levels showed a positive correlation with pro-inflammatory cytokines IL-2 and IL-6.
  • CSF osteopontin levels demonstrated a negative correlation with the anti-inflammatory molecule IL-1 receptor antagonist (IL-1ra).

Conclusions:

  • Osteopontin expression in CSF appears to increase in proximity to acute MS relapses.
  • Elevated osteopontin during relapses is associated with increased pro-inflammatory mediators and decreased anti-inflammatory molecules.
  • These findings reinforce the role of osteopontin in the inflammatory processes of acute MS relapses.