Comprehensive analysis of microRNA profiles in multiple sclerosis including next-generation sequencing

Author:

Keller Andreas12,Leidinger Petra1,Steinmeyer Florian34,Stähler Cord2,Franke Andre5,Hemmrich-Stanisak Georg5,Kappel Andreas6,Wright Ian6,Dörr Jan47,Paul Friedemann47,Diem Ricarda8,Tocariu-Krick Beatrice9,Meder Benjamin10,Backes Christina1,Meese Eckart1,Ruprecht Klemens34

Affiliation:

1. Department of Human Genetics, Saarland University, Germany

2. Siemens Healthcare, Germany

3. Department of Neurology, Charité – Universitätsmedizin Berlin, Germany

4. Clinical and Experimental Multiple Sclerosis Research Center, Charité – Universitätsmedizin Berlin, Germany

5. Institute of Clinical Molecular Biology, Christian-Albrechts Universität Kiel, Germany

6. Siemens Healthcare Diagnostics, USA

7. NeuroCure Clinical Research Center, Charité – Universitätsmedizin Berlin, Germany

8. Department of Neurooncology, Heidelberg University, Germany

9. Department of Neurology, Saarland University, Germany

10. Department of Internal Medicine II, Heidelberg University, Germany

Abstract

Background: MicroRNAs (miRNAs) are short, noncoding RNAs with gene regulatory functions whose expression profiles may serve as disease biomarkers. Objective: The objective of this study was to perform a comprehensive analysis of miRNA expression profiles in blood of patients with a clinically isolated syndrome (CIS) or relapsing–remitting multiple sclerosis (RRMS) including next-generation sequencing (NGS). Methods: miRNA expression was analyzed in whole blood samples from treatment-naïve patients with CIS ( n = 25) or RRMS ( n = 25) and 50 healthy controls by NGS, microarray analysis, and quantitative real-time polymerase chain reaction (qRT-PCR). Results: In patients with CIS/RRMS, NGS and microarray analysis identified 38 and eight significantly deregulated miRNAs, respectively. Three of these miRNAs were found to be significantly up- (hsa-miR-16-2-3p) or downregulated (hsa-miR-20a-5p, hsa-miR-7-1-3p) by both methods. Another five of the miRNAs significantly deregulated in the NGS screen showed the same direction of regulation in the microarray analysis. qRT-PCR confirmed the direction of regulation for all eight and was significant for three miRNAs. Conclusions: This study identifies a set of miRNAs deregulated in CIS/RRMS and reconfirms the previously reported underexpression of hsa-miR-20a-5p in MS. hsa-miR-20a-5p and the other validated miRNAs may represent promising candidates for future evaluation as biomarkers for MS and could be of relevance in the pathophysiology of this disease.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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