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Updated: Jun 27, 2025

Cerebrospinal Fluid MicroRNA Profiling Using Quantitative Real Time PCR
Published on: January 22, 2014
Circulating microRNAs May Be Predictive of Degenerative Cervical Myelopathy
Srikanth N Divi1, Dessislava Z Markova2, Nicholas D D'Antonio2
1Department of Orthopaedic Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL.
Patients with degenerative cervical myelopathy (DCM) show unique circulating microRNAs (miRNAs) and inflammatory markers. These biomarkers may offer new avenues for diagnostic testing and therapeutic interventions for DCM.
Area of Science:
- Basic Science
- Biomarkers
- Neuroscience
Background:
- Degenerative cervical myelopathy (DCM) diagnosis relies on clinical assessment and imaging.
- Currently, no specific serum markers exist for DCM diagnosis.
- Identifying novel biomarkers is crucial for improved DCM management.
Purpose of the Study:
- To identify a unique serum profile of circulating miRNAs and inflammatory markers in DCM patients.
- To compare these profiles against healthy controls (HC).
- To explore potential diagnostic and therapeutic targets for DCM.
Main Methods:
- Collected venous blood from DCM patients and age/gender-matched HC.
- Extracted and screened miRNAs to identify dysregulation in DCM.
- Utilized RT-qPCR for specific miRNA analysis (miR-223-3p, miR-451a).
- Performed bioinformatics analysis for gene networks and miRNA targets.
- Assessed serum inflammatory profiles using a pro-inflammatory panel.
Main Results:
- Two miRNAs, miR-223-3p (upregulated) and miR-451a (downregulated), were differentially expressed in DCM.
- Bioinformatics identified a neurological disease-associated gene network with miR-233-3p targeting over 100 genes.
- Significant upregulation of pro-inflammatory cytokines was observed in DCM patients compared to HC.
- Thirty-six DCM patients and 35 HC were enrolled.
Conclusions:
- DCM patients exhibit a distinct circulating miRNA signature and inflammatory profile.
- These findings suggest potential utility of identified miRNAs as diagnostic or prognostic markers.
- The identified biomarkers may represent future therapeutic targets for degenerative cervical myelopathy.
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