Profiling of serum and urinary microRNAs in children with atopic dermatitis

PLoS One. 2014 Dec 22;9(12):e115448. doi: 10.1371/journal.pone.0115448. eCollection 2014.

Abstract

Background: Atopic dermatitis (AD) is the most prevalent chronic inflammatory skin disease in children characterized by dermatitis and pruritus. MicroRNAs (miRNAs) have been shown as great potential biomarkers for disease fingerprints to predict prognostics. We aimed to identify miRNA signature from serum and urine for the prognosis of AD patient by genome-wide miRNA profiling analysis.

Methods: Serum and urine from 30 children with AD and 28 healthy children were collected and their genome-wide miRNA expression profiles were measured by TaqMan-based array and confirmed by quantitative real-time PCR. Inflammatory factors in serum were detected by Antibody Array System.

Results: miR-203 and miR-483-5p were significantly up-regulated in serum of children with AD compared with healthy children. The level of miR-483-5p in serum was significantly associated with other atopic conditions, such as rhinitis and/or asthma. However, miR-203 was markedly decreased in urine of children with AD compared with healthy children. Down-regulated miR-203 in urine was significant associated with abnormal level of serum IgE in AD patients. 7 inflammatory factors in serum were altered in children with AD compared with healthy children. Up-regulated miR-203 in serum was significantly associated with increased sTNFRI and sTNFRII.

Conclusions: Up-regulated miR-483-5p in serum may be indicative of other atopic conditions in children with AD. Down-regulated miR-203 in urine may serve as a biomarker for the severity of inflammation in children with AD.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood*
  • Biomarkers / urine*
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Dermatitis, Atopic / blood
  • Dermatitis, Atopic / genetics*
  • Dermatitis, Atopic / urine
  • Female
  • Gene Expression Profiling
  • Humans
  • Infant
  • Inflammation Mediators / analysis
  • Male
  • MicroRNAs / blood*
  • MicroRNAs / urine*
  • Prognosis
  • Real-Time Polymerase Chain Reaction
  • Up-Regulation

Substances

  • Biomarkers
  • Inflammation Mediators
  • MicroRNAs

Grants and funding

This work was supported by Public Welfare Research Fund for Healthcare (201202013) and Innovative Research Teams in Universities, Liaoning Bureau of Education (LT2012012). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.