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Significant reduction of long non-coding RNAs expression in bipolar disorder
Long non-coding RNAs (lncRNAs) have been recently emerged as critical modulators of oxidative stress pathway. Likewise, rising evidence currently highlights dysfunction of oxidative stress pathways in bipolar disorder (BD) patients. In the current study, we evaluated the expression levels of H19, SC...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9004165/ https://www.ncbi.nlm.nih.gov/pubmed/35410190 http://dx.doi.org/10.1186/s12888-022-03899-y |
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author | Maloum, Zahra Taheri, Mohammad Ghafouri-Fard, Soudeh Shirvani-Farsani, Zeinab |
author_facet | Maloum, Zahra Taheri, Mohammad Ghafouri-Fard, Soudeh Shirvani-Farsani, Zeinab |
author_sort | Maloum, Zahra |
collection | PubMed |
description | Long non-coding RNAs (lncRNAs) have been recently emerged as critical modulators of oxidative stress pathway. Likewise, rising evidence currently highlights dysfunction of oxidative stress pathways in bipolar disorder (BD) patients. In the current study, we evaluated the expression levels of H19, SCAL1 (LUCAT1), RMST, MEG3 and MT1DP lncRNAs in the PBMC from 50 patients with BD and 50 control subjects (male/female ratio in each group: 70%/30%). Expression levels of SCAL1, RMST and MEG3 but not H19 and MT1DP were considerably decreased in BD patients compared with healthy individuals. Such significant decrease in the expression of MEG3, RMST and SCAL1 was only reported in male BD patients compared with male controls. Substantial pairwise correlations were observed between expression levels of these lncRNAs in BD subjects. The area under curve values for RMST, MEG3 and SCAL1 were 0.70, 0.63 and 0.61 respectively. On the basis of this finding, RMST had the best efficiency in the discrimination of disease status between BD patients and controls. Taken together, the current results suggest a role for MEG3, RMST and SCAL1 lncRNAs in the pathogenesis of BD. In addition, peripheral expression levels of these lncRNAs might serve as potential peripheral markers for BD. |
format | Online Article Text |
id | pubmed-9004165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90041652022-04-13 Significant reduction of long non-coding RNAs expression in bipolar disorder Maloum, Zahra Taheri, Mohammad Ghafouri-Fard, Soudeh Shirvani-Farsani, Zeinab BMC Psychiatry Research Long non-coding RNAs (lncRNAs) have been recently emerged as critical modulators of oxidative stress pathway. Likewise, rising evidence currently highlights dysfunction of oxidative stress pathways in bipolar disorder (BD) patients. In the current study, we evaluated the expression levels of H19, SCAL1 (LUCAT1), RMST, MEG3 and MT1DP lncRNAs in the PBMC from 50 patients with BD and 50 control subjects (male/female ratio in each group: 70%/30%). Expression levels of SCAL1, RMST and MEG3 but not H19 and MT1DP were considerably decreased in BD patients compared with healthy individuals. Such significant decrease in the expression of MEG3, RMST and SCAL1 was only reported in male BD patients compared with male controls. Substantial pairwise correlations were observed between expression levels of these lncRNAs in BD subjects. The area under curve values for RMST, MEG3 and SCAL1 were 0.70, 0.63 and 0.61 respectively. On the basis of this finding, RMST had the best efficiency in the discrimination of disease status between BD patients and controls. Taken together, the current results suggest a role for MEG3, RMST and SCAL1 lncRNAs in the pathogenesis of BD. In addition, peripheral expression levels of these lncRNAs might serve as potential peripheral markers for BD. BioMed Central 2022-04-12 /pmc/articles/PMC9004165/ /pubmed/35410190 http://dx.doi.org/10.1186/s12888-022-03899-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Maloum, Zahra Taheri, Mohammad Ghafouri-Fard, Soudeh Shirvani-Farsani, Zeinab Significant reduction of long non-coding RNAs expression in bipolar disorder |
title | Significant reduction of long non-coding RNAs expression in bipolar disorder |
title_full | Significant reduction of long non-coding RNAs expression in bipolar disorder |
title_fullStr | Significant reduction of long non-coding RNAs expression in bipolar disorder |
title_full_unstemmed | Significant reduction of long non-coding RNAs expression in bipolar disorder |
title_short | Significant reduction of long non-coding RNAs expression in bipolar disorder |
title_sort | significant reduction of long non-coding rnas expression in bipolar disorder |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9004165/ https://www.ncbi.nlm.nih.gov/pubmed/35410190 http://dx.doi.org/10.1186/s12888-022-03899-y |
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