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Circulating microRNAs as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation
Ischemic stroke (IS) is the majority of strokes which remain the second leading cause of deaths in the last two decades. Circulating microRNAs (miRNAs) have been suggested as potential diagnostic and therapeutic tools for IS by previous studies analyzing their differential expression. However, incon...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357437/ https://www.ncbi.nlm.nih.gov/pubmed/37484808 http://dx.doi.org/10.7150/ijms.83963 |
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author | Wang, Yang Su, Xianwei Leung, Geoffrey Ho Duen Ren, Bohua Zhang, Qiang Xiong, Zhiqiang Zhou, Jingye Yang, Ling Lu, Gang Chan, Wai-Yee Ren, Lijie |
author_facet | Wang, Yang Su, Xianwei Leung, Geoffrey Ho Duen Ren, Bohua Zhang, Qiang Xiong, Zhiqiang Zhou, Jingye Yang, Ling Lu, Gang Chan, Wai-Yee Ren, Lijie |
author_sort | Wang, Yang |
collection | PubMed |
description | Ischemic stroke (IS) is the majority of strokes which remain the second leading cause of deaths in the last two decades. Circulating microRNAs (miRNAs) have been suggested as potential diagnostic and therapeutic tools for IS by previous studies analyzing their differential expression. However, inconclusive and controversial conclusions of these results have to be addressed. In this study, comprehensive analysis and real-world validation were performed to assess the associations between circulating miRNAs and IS. 29 studies with 112 miRNAs were extracted after manual selection and filtering, 12 differentially expressed miRNAs were obtained from our results of meta-analysis. These miRNAs were evaluated in 20 IS patients, compared to 20 healthy subjects. 4 miRNAs (hsa-let-7e-5p, hsa-miR-124-3p, hsa-miR-17-5p, hsa-miR-185-5p) exhibited the significant expression level in IS patient plasma samples. Pathway and biological process enrichment analysis for the target genes of the 4 validated miRNAs identified cellular senescence and neuroinflammation as key post-IS response pathways. The results of our analyses closely correlated with the pathogenesis and implicated pathways observed in IS subjects suggested by the literature, which may provide aid in the development of circulating diagnostic or therapeutic targets for IS patients. |
format | Online Article Text |
id | pubmed-10357437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-103574372023-07-21 Circulating microRNAs as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation Wang, Yang Su, Xianwei Leung, Geoffrey Ho Duen Ren, Bohua Zhang, Qiang Xiong, Zhiqiang Zhou, Jingye Yang, Ling Lu, Gang Chan, Wai-Yee Ren, Lijie Int J Med Sci Research Paper Ischemic stroke (IS) is the majority of strokes which remain the second leading cause of deaths in the last two decades. Circulating microRNAs (miRNAs) have been suggested as potential diagnostic and therapeutic tools for IS by previous studies analyzing their differential expression. However, inconclusive and controversial conclusions of these results have to be addressed. In this study, comprehensive analysis and real-world validation were performed to assess the associations between circulating miRNAs and IS. 29 studies with 112 miRNAs were extracted after manual selection and filtering, 12 differentially expressed miRNAs were obtained from our results of meta-analysis. These miRNAs were evaluated in 20 IS patients, compared to 20 healthy subjects. 4 miRNAs (hsa-let-7e-5p, hsa-miR-124-3p, hsa-miR-17-5p, hsa-miR-185-5p) exhibited the significant expression level in IS patient plasma samples. Pathway and biological process enrichment analysis for the target genes of the 4 validated miRNAs identified cellular senescence and neuroinflammation as key post-IS response pathways. The results of our analyses closely correlated with the pathogenesis and implicated pathways observed in IS subjects suggested by the literature, which may provide aid in the development of circulating diagnostic or therapeutic targets for IS patients. Ivyspring International Publisher 2023-06-04 /pmc/articles/PMC10357437/ /pubmed/37484808 http://dx.doi.org/10.7150/ijms.83963 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Wang, Yang Su, Xianwei Leung, Geoffrey Ho Duen Ren, Bohua Zhang, Qiang Xiong, Zhiqiang Zhou, Jingye Yang, Ling Lu, Gang Chan, Wai-Yee Ren, Lijie Circulating microRNAs as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation |
title | Circulating microRNAs as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation |
title_full | Circulating microRNAs as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation |
title_fullStr | Circulating microRNAs as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation |
title_full_unstemmed | Circulating microRNAs as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation |
title_short | Circulating microRNAs as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation |
title_sort | circulating micrornas as diagnostic biomarkers for ischemic stroke: evidence from comprehensive analysis and real-world validation |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357437/ https://www.ncbi.nlm.nih.gov/pubmed/37484808 http://dx.doi.org/10.7150/ijms.83963 |
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