Impact of disease and treatments on growth and puberty of pediatric patients with inflammatory bowel disease

Digestion. 2012;85(4):308-19. doi: 10.1159/000336766. Epub 2012 Jun 8.

Abstract

Growth retardation, associated with delayed puberty, is a frequent feature in pediatric patients with inflammatory bowel disease (IBD), especially with Crohn's disease. It is mainly induced by malnutrition and the effects of the inflammatory process on the growth hormone/insulin-like growth factor-1 axis or on the growth plate. Therefore, control of disease activity and mucosal healing are paramount to promote growth and adequate pubertal onset. Current therapeutic strategies for maintenance in IBD include anti-inflammatory drugs, immunosuppressives, and, more recently, biologic agents. Although these treatments are efficient in minimizing inflammation and inducing prolonged remission, their long-term effects on growth and final height remain controversial. Furthermore, glucocorticoid therapy, even though very efficient in inducing remission, clearly shows deleterious effects on growth, which is not the case for exclusive enteral nutrition showing comparable results regarding induction of remission. Thus regular assessment of weight, height and pubertal stage is essential in children and adolescents with chronic disease, namely IBD.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adolescent
  • Child
  • Enteral Nutrition
  • Glucocorticoids / adverse effects*
  • Growth Disorders / etiology*
  • Growth Disorders / metabolism
  • Growth Hormone / metabolism
  • Humans
  • Immunosuppressive Agents / adverse effects*
  • Inflammation / complications
  • Inflammation / etiology
  • Inflammation / metabolism
  • Inflammatory Bowel Diseases / complications*
  • Inflammatory Bowel Diseases / drug therapy*
  • Inflammatory Bowel Diseases / metabolism
  • Insulin-Like Growth Factor I / metabolism
  • Malnutrition / complications
  • Malnutrition / etiology
  • Malnutrition / metabolism
  • Puberty, Delayed / etiology*
  • Puberty, Delayed / metabolism

Substances

  • Glucocorticoids
  • Immunosuppressive Agents
  • Insulin-Like Growth Factor I
  • Growth Hormone