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Faecal calprotectin concentrations in children with functional gastrointestinal disorders diagnosed according to the
G Flagstad1, H Helgeland1, T Markestad1
1.Department of Pediatrics, Innlandet Hospital Trust, Lillehammer, Norway.Department of Child and Adolescent Psychiatry, Innlandet Hospital Trust, Gjøvik Norway.Innlandet Hospital Trust, Gjøvik, Norway.
Insights
Faecal calprotectin levels are normal in children with functional gastrointestinal disorders (FGID). This suggests that bowel inflammation is not a primary factor in the development of FGID in pediatric patients.
Area of Science:
- Pediatric Gastroenterology
- Gastrointestinal Motility Disorders
- Inflammatory Markers
Background:
- Functional gastrointestinal disorders (FGID) are common in children, presenting diagnostic challenges.
- Distinguishing FGID from inflammatory bowel disease (IBD) is crucial for appropriate management.
Purpose of the Study:
- To investigate whether faecal calprotectin concentrations differ across various FGID subtypes in pediatric patients.
- To assess the role of intestinal inflammation in the pathophysiology of FGID.
Main Methods:
- A cohort of children aged 4-15 years with recurrent abdominal pain were evaluated.
- FGID diagnoses were established using the Questionnaire on Pediatric Gastrointestinal Symptoms-Rome III.
- Faecal calprotectin levels were quantified in stool samples.
Main Results:
- The majority of FGID patients (89%) had faecal calprotectin levels at or below the lower detection limit (16 mg/kg).
- No significant differences in calprotectin concentrations were observed among different FGID subgroups.
- A small percentage of children (7%) exhibited slightly elevated values.
Conclusions:
- Faecal calprotectin concentrations are consistently within normal limits in children diagnosed with FGID.
- These findings indicate that significant bowel inflammation is unlikely to be a major contributor to FGID pathogenesis.
- The study supports the functional nature of these disorders, differentiating them from inflammatory conditions.
Objective:
To determine if faecal calprotectin concentrations vary with different entities of functional gastrointestinal disorders (FGID) in children.
Methods:
Children (4-15 years) who were consecutively referred by general practitioners to four general paediatric outpatient clinics for the evaluation of recurrent abdominal pain were assessed according to a research protocol which included clinical examination, a minimum set of blood, urine and stool tests, and clinical reassessment after 6-9 months. The diagnoses of FGID were based on the parent version of the Questionnaire on Pediatric Gastrointestinal Symptoms-Rome III.
Results:
Of the 152 patients included, 142 children were diagnosed with FGID. Of these, 126 (89%) provided a stool specimen for quantification of calprotectin. The median calprotectin concentrations were at or lower than 16 mg/kg which was at the lower detection limit and there were no differences between the FGID subgroups. Nine children (7%) had slightly raised values.
Conclusion:
The faecal calprotectin concentration is within normal limits in FGID and does not vary with different FGID entities suggesting that bowel inflammation is not a significant part of the pathogenesis in FGID.
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