The use of exclusive enteral nutrition for induction of remission in children with Crohn's disease demonstrates that disease phenotype does not influence clinical remission

Aliment Pharmacol Ther. 2009 Sep 1;30(5):501-7. doi: 10.1111/j.1365-2036.2009.04067.x. Epub 2009 Jun 15.

Abstract

Background: Exclusive enteral nutrition (EEN) achieves variable remission rates in patients with Crohn's disease (CD).

Aim: To describe our experience of treating CD with an 8-week course of primary EEN and to study factors affecting treatment outcome.

Methods: All CD patients treated with EEN in our centre between 2004 and 2007 were included in the study. Remission was determined by a combination of clinical parameters. Disease phenotype was assigned using published classifications. Inflammatory markers and anthropometry (Z-scores) were calculated before and after treatment.

Results: A total of 114 children were treated (four were excluded). Median age at diagnosis was 11.6 years. Fifty-seven (51.8%) were fed orally whilst 53 (48.2%) were fed by tube. Eighty-eight (80%) achieved remission with consequent reductions in erythrocyte sedimentation rate and C-reactive protein (P < 0.001). Patients in remission had comparative improvements in weight (-1.04 cf. -0.40) and BMI Z-scores (-0.98 cf. -0.03) by the end of treatment (P < 0.001). Individuals with isolated terminal ileal disease (n = 4) had lower remission rates than other locations (P = 0.02). No other significant differences in remission rates for any other disease locations were found.

Conclusions: Exclusive enteral nutrition induces clinical remission, normalization of inflammatory markers and improves weight/BMI Z-scores in most patients. This study demonstrates that disease phenotype should not influence clinicians when commencing patients on EEN.

MeSH terms

  • Adolescent
  • Anthropometry
  • Blood Sedimentation
  • C-Reactive Protein / metabolism
  • Child
  • Child, Preschool
  • Crohn Disease / therapy*
  • Enteral Nutrition*
  • Humans
  • Phenotype
  • Remission Induction* / methods

Substances

  • C-Reactive Protein