Investigation of the miRNA146a and miRNA155 gene expression levels in patients with multiple sclerosis
dc.contributor.author | Shademan, Behrouz | |
dc.contributor.author | Nourazarian, Alireza | |
dc.contributor.author | Nikanfar, Masoud | |
dc.contributor.author | Avci, Cigir Biray | |
dc.contributor.author | Hasanpour, Mehdi | |
dc.contributor.author | Isazadeh, Alireza | |
dc.date.accessioned | 2020-12-01T11:58:46Z | |
dc.date.available | 2020-12-01T11:58:46Z | |
dc.date.issued | 2020 | |
dc.department | Ege Üniversitesi | en_US |
dc.description.abstract | Multiple sclerosis (MS) is a chronic inflammatory disease and the most common neurodegenerative status. MicroRNAs play an important role in macrophage response to inflammatory processes, and alterations in miRNA levels trigger the inactivation of specific T lymphocytes. As a result, these factors can lead to autoimmune diseases such as MS. Therefore, to determine the role of MicroRNA-146a and MicroRNA-155 in MS patients, their expression levels in serum of MS patients were compared with healthy controls. in this study, the expression levels of MicroRNA-146a and MicroRNA-155 in 30 serum samples of MS and healthy patients as a control group. MicroRNA extraction and cDNA synthesis was performed according manufacture protocols. the expression levels of MicroRNAs were evaluated by Real Time-PCR. MicroRNA-146a and MicroRNA-155 levels were increased in patients with MS compared to controls. the results demonstrated that EDSS score are increased with increasing level of MicroRNA-146a and MicroRNA-155. ROC curve analysis showed that the area under curve (AUC) was significant for MicroRNA-146a and MicroRNA-155. Increased expression levels of MicroRNA-146a and MicroRNA-155 may be associated with the pathogenesis of MS disease. If this study is conducted in a larger sample population and the above results can be used to identify patients or control patients who are under medical care. (C) 2020 Elsevier Ltd. All rights reserved. | en_US |
dc.identifier.doi | 10.1016/j.jocn.2020.04.071 | en_US |
dc.identifier.endpage | 193 | en_US |
dc.identifier.issn | 0967-5868 | |
dc.identifier.issn | 1532-2653 | |
dc.identifier.pmid | 32331943 | en_US |
dc.identifier.scopus | 2-s2.0-85083498543 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 189 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.jocn.2020.04.071 | |
dc.identifier.uri | https://hdl.handle.net/11454/62103 | |
dc.identifier.volume | 78 | en_US |
dc.identifier.wos | WOS:000556833000031 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Sci Ltd | en_US |
dc.relation.ispartof | Journal of Clinical Neuroscience | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Multiple Sclerosis (MS) | en_US |
dc.subject | MicroRNA-146a | en_US |
dc.subject | MicroRNA-155 | en_US |
dc.subject | Novel inflammatory biomarkers | en_US |
dc.title | Investigation of the miRNA146a and miRNA155 gene expression levels in patients with multiple sclerosis | en_US |
dc.type | Article | en_US |