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Mucosal microRNAs relate to age and severity of disease in ulcerative colitis
Mikkel Malham1,2, Jaslin P James3,4, Christian Jakobsen1
1The Pediatric Department, Copenhagen University Hospital, Hvidovre 2650, Denmark.
Insights
MicroRNA (miRNA) expression differs between pediatric and adult ulcerative colitis (UC) patients. miRNA levels correlate with UC disease severity, suggesting their potential as biomarkers for inflammation.
Area of Science:
- Gastroenterology
- Molecular Biology
- Immunology
Background:
- MicroRNAs (miRNAs) are implicated in ulcerative colitis (UC) disease activity.
- The link between miRNA expression and the more severe phenotype in pediatric UC is unclear.
Purpose of the Study:
- To investigate the relationship between miRNA expression, age, and disease severity in pediatric and adult UC patients.
- To determine if altered miRNA expression contributes to the distinct disease phenotype in pediatric UC.
Main Methods:
- RT-qPCR analysis of miR-21, miR-31, miR-126, miR-142, and miR-155 in rectal biopsies.
- Comparison of miRNA expression in 30 pediatric and 30 adult UC patients.
- In situ hybridization and image analysis for miR-21 and miR-126 expression localization.
Main Results:
- Adult UC patients showed significantly higher miR-21 expression than pediatric patients.
- miR-31 expression (all patients) and miR-155 expression (pediatric only) inversely correlated with histological disease severity.
- miR-21 and miR-126 expression levels correlated with histological disease severity.
Conclusions:
- miRNA expression in UC is dependent on patient age and disease severity.
- miRNAs may play a role in regulating UC inflammation.
- miRNAs show potential as biomarkers for monitoring UC disease severity.
Abstract:
Despite significant evidence that the expression of several microRNAs (miRNAs) impacts disease activity in patients with ulcerative colitis (UC), it remains unknown if the more severe disease phenotype seen in pediatric onset UC can be explained by an altered miRNA expression. In this study, we assessed the relationship between miRNA expression, age, and disease severity in pediatric and adult patients with UC. Using RT-qPCR, we analyzed the expression of miR-21, miR-31, miR-126, miR-142 and miR-155 in paraffin embedded rectum biopsies from 30 pediatric and 30 adult-onset UC patients. We found that lesions from adult patients had significantly higher expression levels of miR-21 compared to pediatric patients and that the expression levels of miR-31 (all patients) and miR-155 (pediatric patients only) correlated inversely with histological assessed disease severity. Using in situ hybridization followed by image analysis, the expression level estimates of miR-21 and miR-126 correlated with histological assessed disease severity. In conclusion, we found that the expression of miRNAs depends on the age of the patient and/or the severity of the disease, suggesting that miRNAs may contribute to the regulation of inflammation in UC and could be useful biomarkers in the surveillance of disease severity.
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