Pathophysiology and management of abnormal growth in children with chronic inflammatory bowel disease

S F Ahmed, C Farquharson, P McGrogan, R K Russell

Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

Abstract

Many children with a variety of chronic diseases suffer from a variable component of chronic inflammation and often have co-existing growth retardation. The aetiology of this growth retardation may be multifactorial and in a condition such as inflammatory bowel disease it includes the effects of the disease on nutrition as well as the effect of drugs such as glucocorticoids. Growth is primarily regulated through the endocrine and paracrine component of the GH/IGF-1 axis which may be modulated by other factors such as sex steroids. There is increasing evidence that this axis may be affected in children with chronic inflammation. An improved understanding of the GH/IGF-1 axis and how it is affected in chronic inflammation will lead to an improved rationale for developing therapeutic regimens that can improve growth in those children whose growth does not improve despite optimal management of the disease. This review will illustrate these aspects by concentrating primarily on the pathophysiology of growth retardation in inflammatory bowel disease and possible interventions for improving growth.
Original languageEnglish
Title of host publicationNutrition and Growth
EditorsR Shamir, D Turck, M Phillip
Place of PublicationBasel
PublisherKarger
Pages142-8
Number of pages7
ISBN (Print)978-3-318-02265-0
DOIs
Publication statusPublished - 2013
Event1st International Conference on Nutrition and Growth - Paris, France
Duration: 1 Mar 20123 Mar 2012

Publication series

NameWorld review of nutrition and dietetics
PublisherKarger
Volume106

Conference

Conference1st International Conference on Nutrition and Growth
CountryFrance
CityParis
Period1/03/123/03/12

Fingerprint Dive into the research topics of 'Pathophysiology and management of abnormal growth in children with chronic inflammatory bowel disease'. Together they form a unique fingerprint.

Cite this