4.3 Article

Oligoclonal IgM bands in the cerebrospinal fluid of patients with relapsing MS to inform long-term MS disability

Journal

MULTIPLE SCLEROSIS JOURNAL
Volume 27, Issue 11, Pages 1706-1716

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/1352458520981910

Keywords

Multiple sclerosis; cerebrospinal fluid; inflammation; neurodegeneration; disability

Funding

  1. Red Espanola de Esclerosis Multiple (REEM) [Retic16: RD16/0015/0002, RD16/0015/0003, RD12/0032/0002, RD12/0060/01-02]
  2. Proyecto de Investigacion en Salud [FIS 2015. PI15/00587, FIS2015: PI15/043915, FIS 2018 PI18/01030]
  3. Instituto de Salud Carlos III-Subdireccion General de Evaluacion
  4. Fondo Europeo de Desarrollo Regional (FEDER, Otra manera de hacer Europa)
  5. Fundacio Cellex

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This study investigated the role of cerebrospinal fluid (CSF) markers in predicting long-term multiple sclerosis outcomes, with the presence of oligoclonal IgM bands (OCMB) associated with unfavorable long-term outcomes. These findings suggest that OCMB should be determined in relapsing MS patients to inform long-term prognosis.
Background: Prognostic markers are needed to guide multiple sclerosis (MS) management in the context of large availability of disease-modifying drugs (DMDs). Objective: To investigate the role of cerebrospinal fluid (CSF) markers to inform long-term MS outcomes. Methods: Demographic features, IgM index, oligoclonal IgM bands (OCMB), lipid-specific OCMB, CSF neurofilament light chain protein levels, expanded disability status scale (EDSS), relapses and DMD use over the study period and peripapillary retinal nerve fiber layer (pRNFL) and ganglion cell plus inner plexiform layer (GCIPL) thicknesses in non-optic neuritis eyes (end of follow-up) were collected from relapsing MS (RMS) patients with CSF obtained <= 2 years after MS onset prospectively followed at the Hospital Clinic of Barcelona. We assessed associations between CSF markers and MS outcomes using multivariable models. Results: A total of 89 patients (71 females; median 32.9 years of age) followed over a median of 9.6 years were included. OCMB were associated with a 33% increase in the annualized relapse rate (ARR; p = 0.06), higher odds for high-efficacy DMDs use (OR = 4.8; 95% CI = (1.5, 16.1)), thinner pRNFL (beta = -4.4; 95% CI = (-8.6, -0.2)) and GCIPL (beta = -2.9; 95% CI = (-5.9, +0.05)), and higher rates to EDSS > 3.0 (HR = 4.4; 95% CI = (1.6, 11.8)) and EDSS > 4.0 (HR = 5.4; 95% CI = (1.1, 27.1)). No overall associations were found for other CSF markers. Conclusion: The presence of OCMB was associated with unfavorable long-term outcomes. OCMB should be determined in RMS to inform long-term prognosis.

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