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The role of micro-RNAs in neuropathic pain—a scoping review
Neuropathic pain can be caused by a lesion or disease of the somatosensory system characterised by pathological neuro-immune alterations. At a molecular level, microRNAs (miRNAs) act as regulators of gene expression orchestrating both immune and neuronal processes. Thus, miRNAs may act as essential...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624461/ https://www.ncbi.nlm.nih.gov/pubmed/37928202 http://dx.doi.org/10.1097/PR9.0000000000001108 |
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author | Kovanur Sampath, Kesava Belcher, Suzie Hales, James Thomson, Oliver P. Farrell, Gerard Gisselman, Angela Spontelli Katare, Rajesh Tumilty, Steve |
author_facet | Kovanur Sampath, Kesava Belcher, Suzie Hales, James Thomson, Oliver P. Farrell, Gerard Gisselman, Angela Spontelli Katare, Rajesh Tumilty, Steve |
author_sort | Kovanur Sampath, Kesava |
collection | PubMed |
description | Neuropathic pain can be caused by a lesion or disease of the somatosensory system characterised by pathological neuro-immune alterations. At a molecular level, microRNAs (miRNAs) act as regulators of gene expression orchestrating both immune and neuronal processes. Thus, miRNAs may act as essential modulators of processes for the establishment and maintenance of neuropathic pain. The objective/aims of this scoping review was to explore and chart the literature to identify miRNAs that are dysregulated in neuropathic pain. The following databases were searched from inception to March 2023: PubMed, EBSCO, CINAHL, Cochrane Library, and SCOPUS. Two independent reviewers screened, extracted data, and independently assessed the risk of bias in included studies. The JBI critical appraisal checklist was used for critical appraisal. A narrative synthesis was used to summarise the evidence. Seven studies (total of 384 participants) that met our eligibility criteria were included in this scoping review. Our review has identified different miRNAs that are commonly involved in the chronic neuropathic pain conditions including miR-132, miR-101, and miR-199a. Our review findings further suggest that expression of miRNAs to be significantly associated with increased diabetic disease duration, HbA1C levels, and fibrinogen levels. Our review findings suggest that there is clear association between miRNA expression and chronic neuropathic pain conditions. Therefore, increasing the specificity by selecting a candidate miRNA and identifying its target mRNA is an area of future research. |
format | Online Article Text |
id | pubmed-10624461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-106244612023-11-04 The role of micro-RNAs in neuropathic pain—a scoping review Kovanur Sampath, Kesava Belcher, Suzie Hales, James Thomson, Oliver P. Farrell, Gerard Gisselman, Angela Spontelli Katare, Rajesh Tumilty, Steve Pain Rep Review Neuropathic pain can be caused by a lesion or disease of the somatosensory system characterised by pathological neuro-immune alterations. At a molecular level, microRNAs (miRNAs) act as regulators of gene expression orchestrating both immune and neuronal processes. Thus, miRNAs may act as essential modulators of processes for the establishment and maintenance of neuropathic pain. The objective/aims of this scoping review was to explore and chart the literature to identify miRNAs that are dysregulated in neuropathic pain. The following databases were searched from inception to March 2023: PubMed, EBSCO, CINAHL, Cochrane Library, and SCOPUS. Two independent reviewers screened, extracted data, and independently assessed the risk of bias in included studies. The JBI critical appraisal checklist was used for critical appraisal. A narrative synthesis was used to summarise the evidence. Seven studies (total of 384 participants) that met our eligibility criteria were included in this scoping review. Our review has identified different miRNAs that are commonly involved in the chronic neuropathic pain conditions including miR-132, miR-101, and miR-199a. Our review findings further suggest that expression of miRNAs to be significantly associated with increased diabetic disease duration, HbA1C levels, and fibrinogen levels. Our review findings suggest that there is clear association between miRNA expression and chronic neuropathic pain conditions. Therefore, increasing the specificity by selecting a candidate miRNA and identifying its target mRNA is an area of future research. Wolters Kluwer 2023-11-02 /pmc/articles/PMC10624461/ /pubmed/37928202 http://dx.doi.org/10.1097/PR9.0000000000001108 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Kovanur Sampath, Kesava Belcher, Suzie Hales, James Thomson, Oliver P. Farrell, Gerard Gisselman, Angela Spontelli Katare, Rajesh Tumilty, Steve The role of micro-RNAs in neuropathic pain—a scoping review |
title | The role of micro-RNAs in neuropathic pain—a scoping review |
title_full | The role of micro-RNAs in neuropathic pain—a scoping review |
title_fullStr | The role of micro-RNAs in neuropathic pain—a scoping review |
title_full_unstemmed | The role of micro-RNAs in neuropathic pain—a scoping review |
title_short | The role of micro-RNAs in neuropathic pain—a scoping review |
title_sort | role of micro-rnas in neuropathic pain—a scoping review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624461/ https://www.ncbi.nlm.nih.gov/pubmed/37928202 http://dx.doi.org/10.1097/PR9.0000000000001108 |
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