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Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study
The rising incidence of bone pathologies such as osteoporosis and osteoarthritis is negatively affecting the functional status of millions of patients worldwide. The genetic component of these multifactorial pathologies is far from being fully understood, but in recent years several epigenetic mecha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481273/ https://www.ncbi.nlm.nih.gov/pubmed/34588560 http://dx.doi.org/10.1038/s41598-021-98789-w |
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author | Pertusa, Clara Tarín, Juan J. Cano, Antonio García-Pérez, Miguel Ángel Mifsut, Damián |
author_facet | Pertusa, Clara Tarín, Juan J. Cano, Antonio García-Pérez, Miguel Ángel Mifsut, Damián |
author_sort | Pertusa, Clara |
collection | PubMed |
description | The rising incidence of bone pathologies such as osteoporosis and osteoarthritis is negatively affecting the functional status of millions of patients worldwide. The genetic component of these multifactorial pathologies is far from being fully understood, but in recent years several epigenetic mechanisms involved in the pathophysiology of these bone diseases have been identified. The aim of the present study was to compare the serum expression of four miRNAs in women with hip fragility fracture (OF group), osteoarthritis requiring hip replacement (OA group) and control women (Ctrl group). Serum expression of miR-497-5p, miR-155-5p, miR-423-5p and miR-365-3p was determined in a sample of 23 OA women, 25 OF women and 52 Ctrl women. Data shown that women with bone pathologies have higher expression of miR-497 and miR-423 and lower expression of miR-155 and miR-365 than control subjects. Most importantly, miR-497 was identified as an excellent discriminator between OA group and control group (AUC: 0.89, p < 0.000) and acceptable in distinguishing from the OF group (AUC: 0.76, p = 0.002). Our data suggest that circulating miR-497 may represent a significant biomarker of OA, a promising finding that could contribute towards future early-stage diagnosis of this disease. Further studies are required to establish the role of miR-155, miR-423 and miR-365 in bone pathologies. |
format | Online Article Text |
id | pubmed-8481273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84812732021-09-30 Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study Pertusa, Clara Tarín, Juan J. Cano, Antonio García-Pérez, Miguel Ángel Mifsut, Damián Sci Rep Article The rising incidence of bone pathologies such as osteoporosis and osteoarthritis is negatively affecting the functional status of millions of patients worldwide. The genetic component of these multifactorial pathologies is far from being fully understood, but in recent years several epigenetic mechanisms involved in the pathophysiology of these bone diseases have been identified. The aim of the present study was to compare the serum expression of four miRNAs in women with hip fragility fracture (OF group), osteoarthritis requiring hip replacement (OA group) and control women (Ctrl group). Serum expression of miR-497-5p, miR-155-5p, miR-423-5p and miR-365-3p was determined in a sample of 23 OA women, 25 OF women and 52 Ctrl women. Data shown that women with bone pathologies have higher expression of miR-497 and miR-423 and lower expression of miR-155 and miR-365 than control subjects. Most importantly, miR-497 was identified as an excellent discriminator between OA group and control group (AUC: 0.89, p < 0.000) and acceptable in distinguishing from the OF group (AUC: 0.76, p = 0.002). Our data suggest that circulating miR-497 may represent a significant biomarker of OA, a promising finding that could contribute towards future early-stage diagnosis of this disease. Further studies are required to establish the role of miR-155, miR-423 and miR-365 in bone pathologies. Nature Publishing Group UK 2021-09-29 /pmc/articles/PMC8481273/ /pubmed/34588560 http://dx.doi.org/10.1038/s41598-021-98789-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 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/) . |
spellingShingle | Article Pertusa, Clara Tarín, Juan J. Cano, Antonio García-Pérez, Miguel Ángel Mifsut, Damián Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study |
title | Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study |
title_full | Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study |
title_fullStr | Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study |
title_full_unstemmed | Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study |
title_short | Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study |
title_sort | serum micrornas in osteoporotic fracture and osteoarthritis: a genetic and functional study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481273/ https://www.ncbi.nlm.nih.gov/pubmed/34588560 http://dx.doi.org/10.1038/s41598-021-98789-w |
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