Diagnostic implications of MicroRNAs; 155, 146 a, and 203 lesional expression in alopecia areata: A preliminary

Amany Ibrahim Mustafa1,2, Asmaa Mohamed Al-Refaie1, Ola Samir El-Shimi3

  • 1Department of Dermatology, Venereology and Andrology, Faculty of Medicine, Benha University, Benha, Egypt.

Abstract

Insights

MicroRNAs (miRNAs) are implicated in alopecia areata (AA) pathogenesis. Elevated lesional expression of miRNAs-155, 146a, and 203 correlates with active disease, suggesting their potential as biomarkers for AA activity.

Area of Science:

  • Dermatology
  • Immunology
  • Molecular Biology

Background:

  • Alopecia areata (AA) is an immune-mediated hair follicle disorder with unknown pathophysiology.
  • MicroRNAs (miRNAs) are small noncoding RNAs linked to autoimmune conditions.

Purpose of the Study:

  • To investigate the association between lesional expression of specific miRNAs and AA pathogenesis.
  • To measure the expression levels of miRNAs-155, 146a, and 203 in patchy AA patients.
  • To evaluate the relationship between these miRNAs and AA disease parameters.

Main Methods:

  • Quantitative reverse transcription PCR (RT-qPCR) was used to measure skin expression levels of miRNAs-155, 146a, and 203.
  • The study included 50 patients with patchy AA and 25 healthy controls.
  • Alopecia activity and severity were assessed using established guidelines.

Main Results:

  • Patients with patchy AA showed significantly higher lesional expression of miRNAs-203, 146a, and 155 compared to controls (p < 0.05).
  • Higher miRNA-146a expression was associated with multiple lesions (p < 0.001).
  • Active AA patients exhibited significantly elevated expression of all three miRNAs compared to inactive cases (p < 0.001).

Conclusions:

  • The investigated miRNAs (155, 146a, 203) appear to play a role in the pathogenesis of alopecia areata.
  • These miRNAs may serve as potential indicators of AA disease activity.
  • Further research is necessary to elucidate their precise role and clinical significance.