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Systematic review and meta-analysis of differentially expressed miRNAs in experimental and human temporal lobe epilepsy

Temporal lobe epilepsy (TLE) is a common chronic neurological disease in humans. A number of studies have demonstrated differential expression of miRNAs in the hippocampus of humans with TLE and in animal models of experimental epilepsy. However, the dissimilarities in experimental design have led t...

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Autores principales: Korotkov, A., Mills, J. D., Gorter, J. A., van Vliet, E. A., Aronica, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599629/
https://www.ncbi.nlm.nih.gov/pubmed/28912503
http://dx.doi.org/10.1038/s41598-017-11510-8
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author Korotkov, A.
Mills, J. D.
Gorter, J. A.
van Vliet, E. A.
Aronica, E.
author_facet Korotkov, A.
Mills, J. D.
Gorter, J. A.
van Vliet, E. A.
Aronica, E.
author_sort Korotkov, A.
collection PubMed
description Temporal lobe epilepsy (TLE) is a common chronic neurological disease in humans. A number of studies have demonstrated differential expression of miRNAs in the hippocampus of humans with TLE and in animal models of experimental epilepsy. However, the dissimilarities in experimental design have led to largely discordant results across these studies. Thus, a comprehensive comparison is required in order to better characterize miRNA profiles obtained in various post-status epilepticus (SE) models. We therefore created a database and performed a meta-analysis of differentially expressed miRNAs across 3 post-SE models of epileptogenesis (electrical stimulation, pilocarpine and kainic acid) and human TLE with hippocampal sclerosis (TLE-HS). The database includes data from 11 animal post-SE studies and 3 human TLE-HS studies. A total of 378 differentially expressed miRNAs were collected (274 up-regulated and 198 down-regulated) and analyzed with respect to the post-SE model, time point and animal species. We applied the novel robust rank aggregation method to identify consistently differentially expressed miRNAs across the profiles. It highlighted common and unique miRNAs at different stages of epileptogenesis. The pathway analysis revealed involvement of these miRNAs in key pathogenic pathways underlying epileptogenesis, including inflammation, gliosis and deregulation of the extracellular matrix.
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spelling pubmed-55996292017-09-15 Systematic review and meta-analysis of differentially expressed miRNAs in experimental and human temporal lobe epilepsy Korotkov, A. Mills, J. D. Gorter, J. A. van Vliet, E. A. Aronica, E. Sci Rep Article Temporal lobe epilepsy (TLE) is a common chronic neurological disease in humans. A number of studies have demonstrated differential expression of miRNAs in the hippocampus of humans with TLE and in animal models of experimental epilepsy. However, the dissimilarities in experimental design have led to largely discordant results across these studies. Thus, a comprehensive comparison is required in order to better characterize miRNA profiles obtained in various post-status epilepticus (SE) models. We therefore created a database and performed a meta-analysis of differentially expressed miRNAs across 3 post-SE models of epileptogenesis (electrical stimulation, pilocarpine and kainic acid) and human TLE with hippocampal sclerosis (TLE-HS). The database includes data from 11 animal post-SE studies and 3 human TLE-HS studies. A total of 378 differentially expressed miRNAs were collected (274 up-regulated and 198 down-regulated) and analyzed with respect to the post-SE model, time point and animal species. We applied the novel robust rank aggregation method to identify consistently differentially expressed miRNAs across the profiles. It highlighted common and unique miRNAs at different stages of epileptogenesis. The pathway analysis revealed involvement of these miRNAs in key pathogenic pathways underlying epileptogenesis, including inflammation, gliosis and deregulation of the extracellular matrix. Nature Publishing Group UK 2017-09-14 /pmc/articles/PMC5599629/ /pubmed/28912503 http://dx.doi.org/10.1038/s41598-017-11510-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Korotkov, A.
Mills, J. D.
Gorter, J. A.
van Vliet, E. A.
Aronica, E.
Systematic review and meta-analysis of differentially expressed miRNAs in experimental and human temporal lobe epilepsy
title Systematic review and meta-analysis of differentially expressed miRNAs in experimental and human temporal lobe epilepsy
title_full Systematic review and meta-analysis of differentially expressed miRNAs in experimental and human temporal lobe epilepsy
title_fullStr Systematic review and meta-analysis of differentially expressed miRNAs in experimental and human temporal lobe epilepsy
title_full_unstemmed Systematic review and meta-analysis of differentially expressed miRNAs in experimental and human temporal lobe epilepsy
title_short Systematic review and meta-analysis of differentially expressed miRNAs in experimental and human temporal lobe epilepsy
title_sort systematic review and meta-analysis of differentially expressed mirnas in experimental and human temporal lobe epilepsy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599629/
https://www.ncbi.nlm.nih.gov/pubmed/28912503
http://dx.doi.org/10.1038/s41598-017-11510-8
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