Evaluation of faecal calprotectin as a valuable non-invasive marker in distinguishing gut pathogens in young children with acute gastroenteritis
Language English Country Norway Media print
Document type Journal Article
PubMed
20412103
DOI
10.1111/j.1651-2227.2010.01843.x
PII: APA1843
Knihovny.cz E-resources
- MeSH
- Acute Disease MeSH
- Bacterial Infections diagnosis MeSH
- Biomarkers metabolism MeSH
- Diagnosis, Differential MeSH
- Feces chemistry MeSH
- Gastroenteritis diagnosis microbiology virology MeSH
- Infant MeSH
- Leukocyte L1 Antigen Complex metabolism MeSH
- Humans MeSH
- Child, Preschool MeSH
- Prospective Studies MeSH
- Diarrhea etiology MeSH
- ROC Curve MeSH
- Sensitivity and Specificity MeSH
- Case-Control Studies MeSH
- Virus Diseases diagnosis MeSH
- Check Tag
- Infant MeSH
- Humans MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- Leukocyte L1 Antigen Complex MeSH
AIM: The aim of the study is to evaluate faecal calprotectin (f-CP) in children ≤3 years of age with acute gastroenteritis (AG) as an early predictor of bacterial inflammation. METHODS: We prospectively analysed f-CP levels and diagnostic workup in 107 consecutive children (66 AG, 41 controls). RESULTS: Children with bacterial AG (BAG) was found to have higher diarrheal frequency (p < 0.01), fever (p < 0.01), erythrocyte sedimentation rate (p < 0.001), white blood count (p < 0.01) and C-reactive protein (CRP) (p < 0.001) compared with viral AG (VAG). Vomiting was frequent in VAG (p < 0.001). f-CP negatively correlated with age in controls (r = -0.5998). BAG demonstrated significantly higher f-CP levels [median, 219 μg/g, interquartile range (IQR): 119-350.2] compared with VAG (49.3 μg/g, IQR: 8.8-131.1) as well as controls (26.5 μg/g, IQR: 14.9-55.1) (p < 0.001). VAG and control f-CP levels were similar. f-CP was the best-rated marker of BAG with a diagnostic accuracy of 92%. Receiver-operator characteristic analysis revealed an area under curve of 0.95 for identifying BAG; sensitivity and specificity of f-CP were 93% and 88%, respectively, at an adjusted cut-off point of 103.9 μg/g faeces. Combined f-CP and CRP yield improved diagnostic accuracy of 94% for BAG. CONCLUSION: f-CP facilitates early discrimination between bacterial and viral causes of AG in young children. Combining f-CP with CRP increases the diagnostic power of diagnosing BAG.
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