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Updated: Feb 9, 2026

Circulating MicroRNA Quantification Using DNA-binding Dye Chemistry and Droplet Digital PCR
Published on: June 26, 2016
Circulating microRNAs as potential diagnostic biomarkers for osteoporosis
Abdullah Y Mandourah1,2, Lakshminarayan Ranganath3, Roger Barraclough4
1Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, The William Henry Duncan Building, 6 West Derby Street, Liverpool, L7 8TX, United Kingdom.
Abstract:
Osteoporosis is the most common age-related bone disease worldwide and is usually clinically asymptomatic until the first fracture happens. MicroRNAs are critical molecular regulators in bone remodelling processes and are stabilised in the blood. The aim of this project was to identify circulatory microRNAs associated with osteoporosis using advanced PCR arrays initially and the identified differentially-expressed microRNAs were validated in clinical samples using RT-qPCR. A total of 161 participants were recruited and 139 participants were included in this study with local ethical approvals prior to recruitment. RNAs were extracted, purified, quantified and analysed from all serum and plasma samples. Differentially-expressed miRNAs were identified using miRNA PCR arrays initially and validated in 139 serum and 134 plasma clinical samples using RT-qPCR. Following validation of identified miRNAs in individual clinical samples using RT-qPCR, circulating miRNAs, hsa-miR-122-5p and hsa-miR-4516 were statistically significantly differentially-expressed between non-osteoporotic controls, osteopaenia and osteoporosis patients. Further analysis showed that the levels of these microRNAs were associated with fragility fracture and correlated with the low bone mineral density in osteoporosis patients. The results show that circulating hsa-miR-122-5p and hsa-miR-4516 could be potential diagnostic biomarkers for osteoporosis in the future.
Insights
Circulating microRNAs, hsa-miR-122-5p and hsa-miR-4516, show potential as diagnostic biomarkers for osteoporosis. These microRNAs are linked to low bone density and fragility fractures in patients.
Area of Science:
- Biochemistry
- Molecular Biology
- Gerontology
Background:
- Osteoporosis is a prevalent age-related bone disease, often asymptomatic until fracture.
- MicroRNAs are key regulators of bone remodeling and are detectable in blood.
- Early detection of osteoporosis is crucial for fracture prevention.
Purpose of the Study:
- To identify circulatory microRNAs associated with osteoporosis.
- To validate potential microRNA biomarkers in clinical samples.
- To explore the correlation of identified microRNAs with bone mineral density and fractures.
Main Methods:
- Serum and plasma RNA extraction and purification from 161 participants.
- Initial screening using advanced microRNA PCR arrays.
- Validation of differentially-expressed microRNAs using quantitative real-time PCR (RT-qPCR).
Main Results:
- hsa-miR-122-5p and hsa-miR-4516 were significantly differentially-expressed in osteoporosis patients.
- These microRNAs correlated with low bone mineral density.
- Elevated levels of these microRNAs were associated with fragility fractures.
Conclusions:
- Circulating hsa-miR-122-5p and hsa-miR-4516 are potential diagnostic biomarkers for osteoporosis.
- These microRNAs may aid in early detection and risk assessment of osteoporosis.
- Further research is warranted to establish their clinical utility.
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