Related Experiment Video
Updated: Feb 16, 2026

10:37
Perturbations of Circulating miRNAs in Irritable Bowel Syndrome Detected Using a Multiplexed High-throughput Gene Expression Platform
Published on: November 30, 2016
8.7K
Plasma microRNA Profile Differentiates Crohn's Colitis From Ulcerative Colitis
Uri Netz1,2,3, Jane Carter1, M Robert Eichenberger1
1Price Institute of Surgical Research, The Hiram C. Polk Jr., MD Department of Surgery, University of Louisville, Louisville, Kentucky.
Inflammatory Bowel Diseases
|December 23, 2017
Summary
Plasma microRNAs (miRNAs) can help distinguish Crohn's colitis (CC) from ulcerative colitis (UC). Two specific miRNAs, miR-598 and miR-642, showed significant differences, offering a potential diagnostic tool for inflammatory bowel disease (IBD).
Area of Science:
- Gastroenterology
- Molecular Biology
- Biomarker Discovery
Background:
- Inflammatory bowel disease (IBD) encompasses Crohn's disease (CD) and ulcerative colitis (UC).
- Accurate differentiation between Crohn's colitis (CC) and UC is crucial for treatment, especially surgical planning.
- Diagnostic ambiguity occurs in up to 15% of IBD cases confined to the colon.
Purpose of the Study:
- To investigate the potential of plasma microRNAs (miRNAs) as biomarkers for differentiating CC from UC.
- To identify specific miRNAs that are differentially expressed between CC and UC patients.
Main Methods:
- Plasma samples were collected from patients with isolated CC and UC.
- Screening of 380 common miRNAs was performed, followed by confirmation of differentially expressed miRNAs using single assays.
- A predictive model was developed and validated using blinded data to assess diagnostic accuracy.
Main Results:
- Seven miRNAs were initially selected for confirmation, with two miRNAs (miR-598 and miR-642) showing consistent differential expression (P = 0.013, P = 0.005).
- The predictive model utilizing these two miRNAs achieved an overall accuracy of 75% in differentiating CC from UC using blinded data.
Conclusions:
- Two plasma miRNAs, miR-598 and miR-642, were identified as potential biomarkers to distinguish CC from UC.
- The findings suggest the feasibility and promise of a plasma miRNA-based assay for differentiating these IBD subtypes.
More Related Videos
Related Concept Videos
MicroRNAs
4.1K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
4.1K
MicroRNAs
24.3K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After...
24.3K

