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.

Abstract

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.