Please use this identifier to cite or link to this item:
http://148.72.244.84/xmlui/handle/xmlui/16616
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Nahidah kzar madhloom | - |
dc.contributor.author | Maan Hasan Salih | - |
dc.contributor.author | Iktefa Abdul Hamid Mohammed saeed | - |
dc.contributor.author | Shimaa Jumaa Abood | - |
dc.date.accessioned | 2025-08-24T06:35:28Z | - |
dc.date.available | 2025-08-24T06:35:28Z | - |
dc.date.issued | 2025-06-25 | - |
dc.identifier.uri | http://148.72.244.84/xmlui/handle/xmlui/16616 | - |
dc.description.abstract | Abstract Background: MicroRNAs (miRNAs) regulate several biological pathways in osteoporosis patients. The study aimed to estimate the correlation of miRNA21, miRNA-422, miRNA‐142-3p, and miR-181c with osteoporosis in premenopausal women. Patients and Methods: This study was performed on 60 osteoporosis premenopausal and 30 healthy women. Determination of osteocalcin (OC), deoxypyridinoline (DPD), and bone-specific alkaline phosphatase (BAP) were done by ELISA, and estimation of miRNA gene expression was done by using qRT-PCR. Results: OC, DPD, and BAP levels indicated a significant decrease in osteoporosis women. In addition, our data showed that miRNA-21 (p=0.0001, r=-0.5585) and miRNA-422 (p=0.0035, r=-0.3715) have a high expression and negative correlation with BMD. Meanwhile, the miRNA-142-3p (p=0.0136, r=0.3089) and miRNA-181c (p=0.0401, r=-0.2685) have decreased expression and positive correlation with BMD value. Conclusion: The results of this study indicated a clear association of miRNA21 and miRNA-422 in osteoporosis thus they may be useful as biomarkers for osteoporosis | en_US |
dc.subject | Osteoporosis, miRNA-21, miRNA-422, miRNA‐142-3p, and miR-181c. | en_US |
dc.title | Estimation of miRNA-21, miRNA422, miRNA‐142-3p, and miR-181c Gene Expression as Potential Biomarkers of Osteoporosis in Premenopausal Women | en_US |
dc.type | Article | en_US |
Appears in Collections: | مجلة ديالى الطبية / Diyala Journal of Medicine |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.