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High-sensitivity C-reactive protein in paediatric inflammatory bowel disease
Marianne Sidoroff1, Riitta Karikoski, Taneli Raivio
1Hospital for Children and Adolescents, University of Helsinki, Helsinki, FIN-00029, Finland. marianne.sidoroff@helsinki.fi
High-sensitivity C-reactive protein (hs-CRP) did not help assess disease activity or glucocorticoid response in children with inflammatory bowel disease (IBD) when standard CRP was undetectable. This finding is crucial for understanding IBD management in pediatric patients.
Area of Science:
- Pediatric Gastroenterology
- Inflammatory Bowel Disease Research
- Biomarker Analysis
Background:
- Inflammatory bowel disease (IBD) management in children requires accurate assessment of disease activity.
- Standard C-reactive protein (CRP) levels are often undetectable in pediatric IBD patients, limiting its utility.
- High-sensitivity C-reactive protein (hs-CRP) is a potential alternative biomarker.
Purpose of the Study:
- To evaluate the utility of hs-CRP in assessing disease activity in pediatric IBD.
- To determine if hs-CRP can predict response to glucocorticoid treatment in pediatric IBD.
- To compare hs-CRP levels in active versus quiescent IBD and in different IBD subtypes.
Main Methods:
- Measured standard CRP and hs-CRP levels in 39 children with IBD undergoing colonoscopy.
- Assessed hs-CRP in 22 children with IBD for glucocorticoid treatment response.
- Included 33 non-IBD pediatric controls; hs-CRP was used when standard CRP was < 5 mg/L.
Main Results:
- Standard CRP was undetectable in 64% of IBD patients undergoing colonoscopy.
- hs-CRP could not differentiate active from quiescent IBD in patients with undetectable standard CRP.
- hs-CRP levels did not differ between glucocorticoid responders and non-responders.
Conclusions:
- hs-CRP measurement is not useful for assessing disease activity in pediatric IBD patients with undetectable standard CRP.
- hs-CRP does not aid in evaluating glucocorticoid treatment response in this population.
- Further research may be needed to identify reliable biomarkers for pediatric IBD activity.
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