miRNAs in cerebrospinal fluid identify patients with MS and specifically those with lipid-specific oligoclonal IgM bands

Author:

Quintana Ester1,Ortega Francisco José2,Robles-Cedeño René1,Villar María Luisa3,Buxó Maria4,Mercader Josep Maria5,Alvarez-Cermeño José Carlos6,Pueyo Neus7,Perkal Héctor7,Fernández-Real José Manuel2,Ramió-Torrentà Lluís1

Affiliation:

1. Girona Neuroimmunology and Multiple Sclerosis Unit (UNIEM), Dr. Josep Trueta University Hospital and Girona Biomedical Research Institute (IDIBGI), Girona, Spain/Red Española de Esclerosis Múltiple (REEM), Madrid, Spain

2. Department of Diabetes, Endocrinology and Nutrition, Girona Biomedical Research Institute (IDIBGI), Girona, Spain

3. Department of Immunology, Hospital Ramón y Cajal, IRYCIS, Madrid, Spain/Red Española de Esclerosis Múltiple (REEM), Madrid, Spain

4. Girona Biomedical Research Institute (IDIBGI), Girona, Spain

5. Joint BSC-CRG-IRB Program in Computational Biology, Barcelona Supercomputing Centre, Barcelona, Spain

6. Red Española de Esclerosis Múltiple (REEM), Madrid, Spain; Department of Neurology, Hospital Ramón y Cajal, IRYCIS, Madrid, Spain

7. Girona Neuroimmunology and Multiple Sclerosis Unit (UNIEM), Dr. Josep Trueta University Hospital and Girona Biomedical Research Institute (IDIBGI), Girona, Spain

Abstract

Background: MicroRNAs (miRNAs) are non-coding RNAs that regulate cellular processes by controlling protein translation and mRNA degradation. Objective: We aimed to explore the miRNA signature of multiple sclerosis (MS) patients versus controls and the possibility that patients with lipid-specific oligolconal IgM bands (LS_OCMB), a predictor of a more severe disease course, may have a distinct profile. Methods: An extensive profile of 754 miRNAs was evaluated in the cerebrospinal fluid (CSF) of 14 women using TaqMan low-density arrays. Differentially expressed miRNAs together with others previously identified in the literature were validated in an extended sample of 86 MS patients (39 LS_OCMB+) and 55 controls. Results: We detected higher levels of miR-150 in MS patients and especially in those with LS_OCMB+. Other miRNAs (miR-328, miR-30a-5p and miR-645) were up-regulated in MS patients compared to controls while miR-21, miR-199a-3p, miR-191, miR-365, miR-106a and miR-146a showed down-regulated expression. Considering only patients with LS_OCMB+, we also detected up-regulation of miR-30a-5p, miR-150 and miR-645 and down-regulation of miR-191 compared to controls. Conclusion: Our study confirms the recent findings regarding the deregulated expression of miR-150 not only with MS but also with the presence of LS_OCMB. This study highlights the potential utility of miRNAs in CSF as biomarkers for MS.

Funder

Instituto Carlos III

Spainish Ministry of Economy and Competitiveness

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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