Prognostic role of intrathecal IgM synthesis in multiple sclerosis: Results from a clinical series

Mult Scler. 2021 Feb;27(2):198-207. doi: 10.1177/1352458520907913. Epub 2020 Feb 24.

Abstract

Background: There is emerging evidence that intrathecal IgM synthesis (ITMS) is a risk factor for conversion to clinically defined multiple sclerosis (CDMS) in clinically isolated syndrome (CIS) patients.

Objectives: The objective of this study is to verify the prognostic role of ITMS as a risk factor for the second clinical attack in patients after the first demyelinating event.

Methods: Monocentric observational study performed on prospectively acquired clinical data and retrospective evaluation of magnetic resonance imaging (MRI) data. ITMS was assessed according to Reiber's non-linear function. We compared time to the second attack by using Kaplan-Meier curves and performed adjustment by Cox regression analysis.

Results: Demographics and clinical data were collected prospectively in a cohort of 68 patients. ITMS occurred in 40% (27/68) of patients who had a higher T1-hypointense lesion load at brain MRI (p = 0.041). In multivariate Cox regression analysis (adjusted for age, sex, baseline Expanded Disability Status Scale, IgG oligoclonal bands and disease-modifying treatment exposure), relapsing-remitting multiple sclerosis (MS) patients with ITMS were at higher risk to experience a second clinical attack (adjusted hazard ratio (aHR) = 6.3, 95% confidence interval (CI) = 2.1-18.4, p = 0.001).

Conclusion: Together with previous studies, our findings support the role of ITMS as a prognostic biomarker in MS.

Keywords: Multiple sclerosis; biomarker; cerebrospinal fluid; intrathecal IgM synthesis; magnetic resonance imaging; oligoclonal bands.

Publication types

  • Observational Study

MeSH terms

  • Disease Progression
  • Humans
  • Immunoglobulin M
  • Magnetic Resonance Imaging
  • Multiple Sclerosis* / diagnostic imaging
  • Oligoclonal Bands
  • Prognosis
  • Retrospective Studies

Substances

  • Immunoglobulin M
  • Oligoclonal Bands