Serum microRNAs in osteoporotic fracture and osteoarthritis: a genetic and functional study
Autor: | Antonio Cano, Miguel Angel García-Pérez, Clara Pertusa, Damián Mifsut, Juan J. Tarín |
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Rok vydání: | 2021 |
Předmět: |
Oncology
medicine.medical_specialty Science Osteoporosis Disease Osteoarthritis Article Internal medicine Hip replacement medicine Humans Bone Aged Multidisciplinary business.industry Incidence (epidemiology) Cartilage Middle Aged medicine.disease Pathophysiology MicroRNAs medicine.anatomical_structure Case-Control Studies Medicine Genetic markers Biomarker (medicine) Epigenetics Female business Biomarkers Osteoporotic Fractures |
Zdroj: | Scientific Reports Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021) |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-021-98789-w |
Popis: | 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 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. |
Databáze: | OpenAIRE |
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