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Identification of circulating microRNA patterns in patients in psoriasis and psoriatic arthritis
Judith Haschka1,2, David Simon3,4, Sara Bayat3,4
1Ludwig Boltzmann Institute of Osteology, I Medical Department at Hanusch Hospital of OEGK, Vienna, Austria.
Objective:
miRNAs are small non-coding RNAs that control gene expression. Specific intra- and extracellular miRNA signatures have been identified in various diseases. Whether certain miRNA signatures are associated with psoriasis (PsO) and PsA is currently unknown. We aimed to search for circulating miRNA signatures associated with PsO and PsA patients.
Methods:
Expression of miRNAs was analysed by reverse transcription quantitative real-time PCR (RT-qPCR) in the serum of PsA, PsO patients and healthy controls. Demographic and disease-specific characteristics and imaging data from hand MRI were recorded. In the discovery phase, 192 miRNA assays were analysed in 48 samples (PsA, PsO, controls: each N = 16). For validation, 17 selected miRNAs were measured in the total population.
Results:
A total of 141 patients and controls were analysed (51 PsA, 40 PsO, 50 controls). In the discovery phase 51 miRNAs in PsO and 64 miRNAs in PsA were down- or upregulated compared with controls, with 33 miRNAs being changed in both (adj. P < 0.05). The 17 top candidates from discovery were assessed in the validation phase, 9 of them discriminated PsA and PsO from controls [area under the curve (AUC) ≥0.70, all P < 0.05]. Four miRNAs (miR-19b-3p, miR-21-5p, miR-92a-3p and let-7b-5p) were significantly differently regulated between PsO and PsA. A combination of these miRNAs increased the AUC to 0.92 in multivariate regression model to discriminate PsO and PsA.
Conclusion:
miRNA signatures in PsA and PsO patients differ from controls. Nine miRNAs were differentially regulated in PsA and PsO patients, five of them previously reported to be involved in bone and cartilage metabolism, indicating an intimate association of psoriatic inflammation and bone/cartilage changes.
Insights
Specific microRNA (miRNA) signatures in the blood can distinguish between psoriasis (PsO) and psoriatic arthritis (PsA) patients and healthy individuals. Four key miRNAs show significant differences between PsO and PsA, aiding in diagnosis.
Area of Science:
- Biochemistry and Molecular Biology
- Immunology
- Genetics
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs regulating gene expression.
- Distinct miRNA profiles are observed in various diseases, but their role in psoriasis (PsO) and psoriatic arthritis (PsA) remains unclear.
- Circulating miRNAs offer potential biomarkers for disease detection and monitoring.
Purpose of the Study:
- To identify specific circulating miRNA signatures associated with PsO and PsA.
- To differentiate between PsO and PsA patients based on their miRNA profiles.
- To explore the relationship between identified miRNAs and disease characteristics.
Main Methods:
- Serum samples from PsA, PsO patients, and healthy controls were analyzed using reverse transcription quantitative real-time PCR (RT-qPCR).
- A discovery phase involved analyzing 192 miRNAs in 48 samples, followed by validation of 17 candidate miRNAs in the total cohort.
- Demographic, clinical, and hand MRI data were collected for correlation analysis.
Main Results:
- Nine miRNAs were found to be differentially regulated in PsA and PsO patients compared to controls.
- Four specific miRNAs (miR-19b-3p, miR-21-5p, miR-92a-3p, and let-7b-5p) showed significant differences between PsO and PsA.
- A combination of these four miRNAs achieved an AUC of 0.92 for discriminating between PsO and PsA.
Conclusions:
- Circulating miRNA signatures effectively differentiate PsA and PsO patients from healthy controls.
- The identified miRNA profiles suggest a link between psoriatic inflammation and bone/cartilage metabolism.
- These findings highlight the potential of miRNAs as diagnostic biomarkers for PsO and PsA.
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