Which PCDAI Version Best Reflects Intestinal Inflammation in Pediatric Crohn Disease?

Dan Turner1, Arie Levine, Thomas D Walters

  • 1*Pediatric Gastroenterology Unit, Shaare Zedek Medical Center, The Hebrew University of Jerusalem †Pediatric Gastroenterology Unit, Wolfson Medical Center, Tel Aviv University, Holon, Israel ‡Hospital for Sick Children, Toronto, Ontario §IWK Health Centre, Halifax, Nova Scotia, Canada ||Children's Hospital, Málaga, Spain ¶Hauner Children's Hospital, Munich, Germany #Children's Hospital of Philadelphia, Philadelphia, PA **Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada ††Connecticut Children's Medical Center, Hartford.

Insights

The weighted Pediatric Crohn's Disease Activity Index (wPCDAI) and PCDAI correlate moderately with endoscopic inflammation in pediatric Crohn's disease. However, no current PCDAI version accurately assesses mucosal healing.

Area of Science:

  • Pediatric Gastroenterology
  • Inflammatory Bowel Disease Research
  • Clinical Trial Analysis

Background:

  • Measuring mucosal inflammation is crucial in pediatric Crohn's disease (CD).
  • Limited data exist correlating Pediatric Crohn's Disease Activity Index (PCDAI) versions with objective measures of inflammation.

Purpose of the Study:

  • To compare four PCDAI versions against endoscopic inflammation (SES-CD), fecal calprotectin, ESR, and CRP.
  • To identify potential cut-off values for PCDAI versions associated with mucosal healing in pediatric CD patients.

Main Methods:

  • Prospective data from the ImageKids and Growth Relapse and Outcomes with Therapy studies were analyzed.
  • 100 children with CD underwent colonoscopy; 145 had fecal calprotectin data at week 12.
  • Four PCDAI versions were compared with SES-CD, fecal calprotectin, ESR, and CRP.

Main Results:

  • All four PCDAI versions showed fair correlation with SES-CD (r=0.42-0.45) and CRP (r=0.32-0.45).
  • The wPCDAI and PCDAI demonstrated superior correlation with blood tests compared to shorter versions.
  • Correlation with fecal calprotectin was poor for all versions; only wPCDAI reached significance (r=0.26).
  • Optimal cut-offs for mucosal healing were <12.5 for wPCDAI (sensitivity 58%, specificity 84%) and <10 for PCDAI (sensitivity 63%, specificity 77%).

Conclusions:

  • The wPCDAI and PCDAI show comparable and fair correlation with endoscopic inflammation measures.
  • These versions are slightly superior to abbreviated and short versions but do not reliably assess mucosal healing.
  • Further research is needed to develop accurate tools for assessing mucosal healing in pediatric CD.
Abstract

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