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Fecal α1-Antitrypsin: A Marker of Intestinal Versus Systemic Inflammation in Pediatric Crohn's Disease?
D Herzog1, E Delvin, E Seidman
1Divisions of Gastroenterology and *Clinical Biochemistry, Department of Pediatrics, Ste-Justine Hospital, University of Montreal, Montreal, Canada.
Insights
Fecal alpha-1 antitrypsin (α1-AT) is not a reliable marker for active Crohn
Area of Science:
- Pediatric Gastroenterology
- Inflammatory Bowel Disease Research
- Biomarker Discovery
Background:
- Crohn's disease (CD) in children often causes growth failure and malnutrition.
- Identifying early, noninvasive relapse markers is crucial for pediatric CD management.
- Fecal alpha-1 antitrypsin (α1-AT) is explored as a potential indicator.
Purpose of the Study:
- To evaluate fecal α1-AT as an early, noninvasive marker for relapse in pediatric Crohn's disease.
- To correlate fecal α1-AT levels with disease activity (P-CDAI) and growth status.
- To compare fecal α1-AT levels in pediatric CD patients with controls.
Main Methods:
- Prospective study of 42 pediatric CD patients over 1 year.
- Monthly assessment of fecal α1-AT, P-CDAI, and growth parameters.
- Comparison of fecal α1-AT levels between relapsed, quiescent, and healthy pediatric groups.
Main Results:
- Fecal α1-AT levels did not differ significantly between active relapse and quiescent CD.
- Children with growth failure showed significantly higher fecal α1-AT, even in remission.
- Elevated fecal α1-AT levels correlated with malnutrition and subclinical disease activity, not overt relapse.
Conclusions:
- Fecal α1-AT is not a reliable marker for clinically active Crohn's disease in children.
- Fecal α1-AT may indicate chronic malnutrition and subclinical disease activity in pediatric CD.
- Further research is needed to clarify the role of fecal α1-AT in pediatric IBD.
Abstract:
: Growth failure and malnutrition are major concerns in pediatric patients with frequent relapses of Crohn's disease (CD). In search of an early, noninvasive marker of relapse, we prospectively examined the relationship between levels of fecal α1-antitrypsin (α1-AT) in comparison with other known inflammatory parameters and disease activity using a pediatric CD Activity Index (P-CDAI), as well as in relation to growth. Forty-two pediatric patients (29 M, 13 F, 7-16 years old, mean 12.8 years) with ileal or ileocolonic CD were prospectively examined at 4 monthly intervals over a 1 year period. Median (interquartile range) fecal α1-AT values did not differ between children in clinical relapse (P-CDAI > 150, n = 10) compared with CD patients (n = 42) with quiescent disease [1.84 (3.67) mg/g versus 1.55 (3.97) mg/g, respectively, p = ns]. However, children with growth failure (n = 14) had a significantly higher fecal α1-AT [3.63 (5.65) mg/g] despite clinical remission [median P-CDAI 22 (72.5)] compared with those with normal growth [1.41 (1.66) mg/g, p = 0.02]. Very high fecal α1-AT levels (>4 mg/g) were not associated with clinically active disease [median P-CDAI 23 (71.5)]. Overall however, levels in CD were significantly higher than that of 17 pediatric control patients with diarrheal disorders unrelated to IBD [0.98 (1.21), p < 0.05]. Fecal α1-AT seems therefore not to be a reliable marker of clinically evident disease activity, but was best correlated with chronic malnutrition and subclinical disease activity.
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