Relationship between mir-126 expression in children with psoriasis, disease progression and therapeutic response

Elvina Murzina1, Victor Dosenko2, Tetiana Drevytska2

  • 1Department of Dermatovenereology, Allergology, Clinical and Laboratory Immunology, Shupyk National Healthcare University of Ukraine, Kyiv, Ukraine.

Insights

MicroRNA-126 (miR-126) levels in children with psoriasis are altered in buccal epithelium and correlate with disease severity and treatment response. Initial miR-126 levels in buccal epithelium can predict therapy outcomes in pediatric psoriasis.

Area of Science:

  • Dermatology
  • Molecular Biology
  • Genetics

Background:

  • Psoriasis is a chronic inflammatory skin condition affecting children.
  • MicroRNAs (miRNAs) play a role in regulating gene expression and are implicated in various diseases, including psoriasis.
  • miR-126 has been identified as a potential biomarker in several conditions, but its role in pediatric psoriasis requires further investigation.

Purpose of the Study:

  • To investigate the expression levels of miR-126 in children with psoriasis.
  • To determine the association between miR-126 expression and psoriasis severity, clinical presentation, and treatment efficacy.
  • To evaluate the potential of miR-126 as a prognostic marker for therapeutic response in pediatric psoriasis.

Main Methods:

  • Quantitative real-time PCR was used to measure miR-126 expression in psoriatic skin lesions and buccal epithelium of 54 children with psoriasis.
  • Correlation analyses were performed to assess the relationship between miR-126 levels and clinical parameters such as psoriasis severity (Body Surface Area - BSA), Psoriasis Area and Severity Index (PASI), and Physician's Global Assessment (PGA).
  • Treatment response (PASI < 75) was evaluated in relation to initial miR-126 levels.

Main Results:

  • miR-126 levels were significantly reduced in the buccal epithelium of children with psoriasis compared to healthy controls.
  • miR-126 expression in psoriatic epidermis varied significantly based on the clinical form and severity (BSA) of psoriasis.
  • Higher initial miR-126 levels in the buccal epithelium were associated with a poorer response to treatment (PASI < 75) and higher rates of treatment failure, particularly in older children and those with higher PGA scores.
  • High miR-126 levels in psoriatic keratinocytes correlated with moderate to severe plaque psoriasis.

Conclusions:

  • miR-126 expression is dysregulated in pediatric psoriasis and is linked to disease characteristics.
  • Initial miR-126 levels in the buccal epithelium serve as a prognostic indicator for treatment response in children with psoriasis.
  • Measuring miR-126 in buccal epithelium may aid in guiding treatment decisions, including the initiation of systemic therapy for pediatric psoriasis.