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Elevated levels of miR-181c and miR-633 in the CSF of patients with MS: A validation study
OBJECTIVE: To validate a previously discovered microRNA (miRNA) panel in the CSF of patients with MS, we now tested the diagnostic value of CSF-derived candidate miRNAs in a case-control study in a larger MS cohort. METHODS: The levels of miR-181c, miR-633, and miR-922 were analyzed in the CSF of 21...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812730/ https://www.ncbi.nlm.nih.gov/pubmed/31575652 http://dx.doi.org/10.1212/NXI.0000000000000623 |
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author | Kramer, Svenja Haghikia, Arash Bang, Claudia Scherf, Kristian Pfanne, Angelika Duscha, Alexander Kaisler, Johannes Gisevius, Barbara Gold, Ralf Thum, Thomas Haghikia, Aiden |
author_facet | Kramer, Svenja Haghikia, Arash Bang, Claudia Scherf, Kristian Pfanne, Angelika Duscha, Alexander Kaisler, Johannes Gisevius, Barbara Gold, Ralf Thum, Thomas Haghikia, Aiden |
author_sort | Kramer, Svenja |
collection | PubMed |
description | OBJECTIVE: To validate a previously discovered microRNA (miRNA) panel in the CSF of patients with MS, we now tested the diagnostic value of CSF-derived candidate miRNAs in a case-control study in a larger MS cohort. METHODS: The levels of miR-181c, miR-633, and miR-922 were analyzed in the CSF of 218 patients with MS and 211 patients with other neurologic diseases (OND) by real-time quantitative reverse transcriptase PCR. RESULTS: CSF levels of both miR-181c (p < 0.001 and miR-633 p < 0.001) were higher in patients with MS patients compared with patients with OND. Both miR-181c (area under the curve [AUC] 0.75, 95% CI 0.70–0.80, p < 0.001) and miR-633 (AUC 0.75, 95% CI 0.68–0.83, p < 0.001) differentiated MS from OND. Combining both miRNAs yielded a sensitivity of 62% and specificity of 89% to differentiate MS from OND. miR-922 was not confirmed to be differentially expressed in this validation cohort. CONCLUSIONS: The results of this so far largest study on CSF-based miRNAs confirm the diagnostic value of miR-181c and miR-633 for MS. The present study may help to extend the diagnostic tools for patients with suspected MS and may add further knowledge to the pathology of the disease. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that CSF-derived miR-181c and miR-633 distinguish patients with MS from patients with OND. |
format | Online Article Text |
id | pubmed-6812730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-68127302019-11-20 Elevated levels of miR-181c and miR-633 in the CSF of patients with MS: A validation study Kramer, Svenja Haghikia, Arash Bang, Claudia Scherf, Kristian Pfanne, Angelika Duscha, Alexander Kaisler, Johannes Gisevius, Barbara Gold, Ralf Thum, Thomas Haghikia, Aiden Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To validate a previously discovered microRNA (miRNA) panel in the CSF of patients with MS, we now tested the diagnostic value of CSF-derived candidate miRNAs in a case-control study in a larger MS cohort. METHODS: The levels of miR-181c, miR-633, and miR-922 were analyzed in the CSF of 218 patients with MS and 211 patients with other neurologic diseases (OND) by real-time quantitative reverse transcriptase PCR. RESULTS: CSF levels of both miR-181c (p < 0.001 and miR-633 p < 0.001) were higher in patients with MS patients compared with patients with OND. Both miR-181c (area under the curve [AUC] 0.75, 95% CI 0.70–0.80, p < 0.001) and miR-633 (AUC 0.75, 95% CI 0.68–0.83, p < 0.001) differentiated MS from OND. Combining both miRNAs yielded a sensitivity of 62% and specificity of 89% to differentiate MS from OND. miR-922 was not confirmed to be differentially expressed in this validation cohort. CONCLUSIONS: The results of this so far largest study on CSF-based miRNAs confirm the diagnostic value of miR-181c and miR-633 for MS. The present study may help to extend the diagnostic tools for patients with suspected MS and may add further knowledge to the pathology of the disease. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that CSF-derived miR-181c and miR-633 distinguish patients with MS from patients with OND. Lippincott Williams & Wilkins 2019-10-01 /pmc/articles/PMC6812730/ /pubmed/31575652 http://dx.doi.org/10.1212/NXI.0000000000000623 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Kramer, Svenja Haghikia, Arash Bang, Claudia Scherf, Kristian Pfanne, Angelika Duscha, Alexander Kaisler, Johannes Gisevius, Barbara Gold, Ralf Thum, Thomas Haghikia, Aiden Elevated levels of miR-181c and miR-633 in the CSF of patients with MS: A validation study |
title | Elevated levels of miR-181c and miR-633 in the CSF of patients with MS: A validation study |
title_full | Elevated levels of miR-181c and miR-633 in the CSF of patients with MS: A validation study |
title_fullStr | Elevated levels of miR-181c and miR-633 in the CSF of patients with MS: A validation study |
title_full_unstemmed | Elevated levels of miR-181c and miR-633 in the CSF of patients with MS: A validation study |
title_short | Elevated levels of miR-181c and miR-633 in the CSF of patients with MS: A validation study |
title_sort | elevated levels of mir-181c and mir-633 in the csf of patients with ms: a validation study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812730/ https://www.ncbi.nlm.nih.gov/pubmed/31575652 http://dx.doi.org/10.1212/NXI.0000000000000623 |
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