Delayed treatment of MS is associated with high CSF levels of IL-6 and IL-8 and worse future disease course

J Neurol. 2018 Nov;265(11):2540-2547. doi: 10.1007/s00415-018-8994-5. Epub 2018 Aug 28.

Abstract

Background: Clinical deterioration of relapsing-remitting MS (RR-MS) patients reflects not only the number and severity of overt inflammatory and demyelinating episodes, but also subtle central damage caused by persistent exposure to inflammatory molecules.

Objective: To explore the correlation between levels of CSF inflammatory molecules at the time of diagnosis and both demographic and clinical characteristics of a large sample of RR-MS patients, as well as the predictive value of cytokine levels on their prospective disease course.

Methods: In 205 patients diagnosed with RR-MS, we measured at the time of diagnosis the CSF levels of inflammatory molecules. Clinical and MRI evaluation was collected at the time of CSF withdrawal and during a median follow-up of 3 years.

Results: The time interval between the first anamnestic episode of focal neurological dysfunction and RR-MS diagnosis was the main factor associated with high CSF levels of IL-6 and IL-8. Furthermore, elevated CSF levels of these cytokines correlated with enhanced risk of clinical and radiological disease reactivation, switch to second-line treatments, and with disability progression in the follow-up.

Conclusions: Delayed diagnosis and treatment initiation are associated with higher CSF levels of IL-6 and IL-8 in RR-MS, leading to worsening disease course and poor response to treatments.

Keywords: CSF cytokines; Disease activity; IL-6; IL-8; Neuroinflammation; RR-MS.

MeSH terms

  • Adult
  • Biomarkers / cerebrospinal fluid
  • Disease Progression
  • Female
  • Follow-Up Studies
  • Humans
  • Interleukin-6 / cerebrospinal fluid*
  • Interleukin-8 / cerebrospinal fluid*
  • Magnetic Resonance Imaging
  • Male
  • Multiple Sclerosis, Relapsing-Remitting / cerebrospinal fluid*
  • Multiple Sclerosis, Relapsing-Remitting / diagnostic imaging
  • Multiple Sclerosis, Relapsing-Remitting / immunology
  • Multiple Sclerosis, Relapsing-Remitting / therapy*
  • Prognosis
  • Prospective Studies
  • Time-to-Treatment

Substances

  • Biomarkers
  • CXCL8 protein, human
  • IL6 protein, human
  • Interleukin-6
  • Interleukin-8