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Published on: October 17, 2013
Clinical disease activity and endoscopic severity correlate poorly in children newly diagnosed with Crohn's disease
Nicholas Carman1, Diane Tomalty2, Peter C Church2
1Children's Hospital of Eastern Ontario, Department of Pediatrics, University of Ottawa, Ottawa, Canada.
Insights
In pediatric Crohn's disease, the weighted Pediatric Crohn's Disease Activity Index (wPCDAI) poorly reflects endoscopic severity. Clinical markers alone are insufficient for assessing disease activity in children with newly diagnosed Crohn's disease.
Area of Science:
- Pediatric Gastroenterology
- Inflammatory Bowel Disease Research
- Clinical Trial Analysis
Background:
- Crohn's disease (CD) treatment increasingly targets mucosal healing.
- Noninvasive measures to assess mucosal healing in pediatric CD require validation.
- Limited data exist on the correlation between clinical indices and endoscopic findings in pediatric CD.
Purpose of the Study:
- To compare endoscopic disease severity with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI) in children with newly diagnosed CD.
- To evaluate the utility of clinical indices and biochemical markers in reflecting endoscopic disease activity.
Main Methods:
- Inclusion of 280 children (≤17 years) newly diagnosed with CD from the Canadian Children Inflammatory Bowel Disease Network.
- Assessment of clinical disease activity using wPCDAI and biochemical parameters.
- Evaluation of endoscopic severity via the Simple Endoscopic Score for CD (SES-CD) and correlation analysis with clinical and biochemical markers.
Main Results:
- A weak correlation was observed between wPCDAI and SES-CD (r = 0.39, P < .001).
- Most wPCDAI components, except stooling, showed weak correlation with SES-CD.
- Routine blood tests did not correlate well with endoscopic severity, and clinical symptoms primarily explained disease activity variations.
Conclusions:
- The wPCDAI demonstrates poor correlation with endoscopic disease activity in newly diagnosed pediatric Crohn's disease.
- Clinical markers alone should not be relied upon to determine disease activity, especially as treatment goals shift towards mucosal healing.
Background And Aims:
Treatment goals in Crohn's disease (CD) have evolved to target mucosal healing. There is now a drive to determine if noninvasive measures can adequately identify the attainment and persistence of this goal. Currently, data describing the relationship between clinical indices and endoscopic appearance in pediatric CD are sparse. Our aim was to compare endoscopic severity with the weighted Pediatric Crohn's Disease Activity Index (wPCDAI) in children with newly diagnosed CD.
Methods:
All children aged ≤17 years newly diagnosed with CD enrolled in an inception cohort at sites of the Canadian Children Inflammatory Bowel Disease Network were eligible. Clinical disease activity at presentation was evaluated by the wPCDAI and conventional biochemical parameters. Severity of disease at ileocolonoscopy was assessed by the simple endoscopic score for CD (SES-CD), with segmental subscores noted. We evaluated the association of SES-CD and disease activity markers using the Pearson test of correlation, the Spearman rank coefficient, and linear regression models.
Results:
Two hundred eighty patients from 11 centers were included in the analysis. The median wPCDAI score was 60 (interquartile range, 40-80; 53% severe). Median SES-CD was 16 (interquartile range 10-22; 51% severe). The wPCDAI correlated weakly with SES-CD (r = .39, P < .001). Examination of the individual components that contribute to the wPCDAI demonstrated weak correlation with the SES-CD for all items apart from stooling (moderate correlation, r = .50, P < .001). Routine blood tests did not correlate well with the SES-CD. In regression models, variation in clinical symptoms accounted for most of the variation in both the wPCDAI and SES-CD, with no additional benefit from routine blood tests.
Conclusions:
In children with newly diagnosed CD, wPCDAI correlates poorly with endoscopic disease activity. As treatment paradigms evolve to target mucosal healing, clinical markers should not be used in isolation to determine disease activity.
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