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Breath Collection from Children for Disease Biomarker Discovery
Published on: February 14, 2019
Anti-Saccharomyces cerevisiae Antibodies as a Prognostic Biomarker in Children With Crohn Disease
Abin Chandrakumar1,2,3, Michael Georgy3, Prasoon Agarwal1,4,5
1Department of Pharmacology and Therapeutics, University of Manitoba.
Insights
Anti-Saccharomyces cerevisiae antibodies (ASCAs) indicate more severe pediatric Crohn disease (CD). However, ASCA immunoglobulin G (IgG) positivity predicts a lower relapse rate in children with CD treated with biologics.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Inflammatory Bowel Disease Research
Background:
- Anti-Saccharomyces cerevisiae antibodies (ASCAs) are potential biomarkers for differentiating Crohn disease (CD) from ulcerative colitis (UC).
- The prognostic significance of ASCA status in pediatric CD patients remains under-investigated.
Purpose of the Study:
- To evaluate the prognostic value of ASCA status in children with CD receiving biologic therapy.
- To assess the association between ASCA status and disease severity and treatment response.
Main Methods:
- A longitudinal prospective observational study of children diagnosed with CD between 2012 and 2018.
- Cox regression models were used to compare anti-tumor necrosis factor (TNF) biologic therapy response between ASCA-positive and ASCA-negative patients.
Main Results:
- ASCA-positive patients exhibited higher risks of moderate-to-severe clinical disease (OR 2.88) and extensive endoscopic disease (OR 3.30) at baseline.
- ASCA immunoglobulin G (IgG)-positive patients treated with biologics showed a significantly lower relapse rate (aHR 0.12).
- A notable proportion (14%) of patients had unstable ASCA values over time.
Conclusions:
- ASCA-positive pediatric CD patients present with more severe clinical and endoscopic disease.
- ASCA IgG status serves as a valuable prognostic marker for children with CD undergoing biologic treatment.
Objective:
Although anti-Saccharomyces cerevisiae antibodies (ASCAs) could be a useful biomarker in differentiating Crohn disease (CD) from ulcerative colitis (UC), their role as prognostic markers in children with CD has been underinvestigated. This longitudinal prospective observational study aimed to assess the prognostic value of ASCA status among children with CD managed using biologics.
Methods:
The study population comprised children with inflammatory bowel disease diagnosed with CD from 2012 to 2018. Cox regression model with adjustment for a priori covariates was used to examine the response to anti-tumor necrosis factor (TNF) biological therapy among ASCA-positive patients in comparison to ASCA-negative patients.
Results:
There were 273 measurements available from the study cohort comprising children with CD, who were followed up for a median duration of 14 months (interquartile range 5-42). ASCA-positive patients had a higher risk for moderate to severe clinical disease (odds ratio 2.88; 95% confidence interval [CI] 1.2-7.55) and extensive endoscopic distribution (odds ratio 3.30; CI 1.12-9.74) at baseline in comparison to ASCA-negative patients, respectively. In comparison to ASCA immunoglobulin G (IgG)-negative patients, ASCA IgG-positive patients who were treated with biologics had a significantly lower relapse rate (adjusted hazard ratio 0.12; CI 0.02-0.93). Ten (14%) patients had an unstable ASCA value with either ASCA immunoglobulin A or ASCA IgG status changing from positive to negative or vice versa.
Conclusions:
ASCA-positive children with CD present with more extensive (endoscopic) and clinically severe disease. ASCA IgG is a useful prognostic marker among children with CD who receive biologics.
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