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J Autism Dev Disord (2008) 38:1066–1071

DOI 10.1007/s10803-007-0482-1

ORIGINAL PAPER

Intestinal Permeability and Glucagon-like peptide-2 in Children


with Autism: A Controlled Pilot Study
Marli A. Robertson Æ David L. Sigalet Æ Jens J. Holst Æ Jon B. Meddings Æ
Julie Wood Æ Keith A. Sharkey

Published online: 29 February 2008


Ó Springer Science+Business Media, LLC 2008

Abstract We measured small intestinal permeability autism, 7 developmentally normal siblings of these chil-
using a lactulose:mannitol sugar permeability test in a dren and 8 healthy, developmentally normal, unrelated
group of children with autism, with current or previous children. Our study did not detect differences in these
gastrointestinal complaints. Secondly, we examined whe- measures of gastrointestinal function in a group of children
ther children with autism had an abnormal glucagon-like with autism.
peptide-2 (GLP-2) response to feeding. Results were
compared with sibling controls and children without Keywords Autism  Nutrition  Intestinal permeability 
developmental disabilities. We enrolled 14 children with Glucagon-like peptide 2

M. A. Robertson
Department of Pediatrics, University of Calgary, Calgary, AB,
Canada Introduction
M. A. Robertson (&)
Alberta Children’s Hospital, 2888 Shaganappi Trail NW, Autism is a complex developmental disorder diagnosed on
Calgary, AB, Canada T3B 6A8 the basis of behavioral symptoms that typically appear
e-mail: marli.robertson@calgaryhealthregion.ca during the first 3 years of life. Autism is one of five dis-
orders coming under the umbrella of Pervasive
D. L. Sigalet  K. A. Sharkey
Institute of Infection, Immunity and Inflammation, Developmental Disorders (PDDs) or autistic spectrum
University of Calgary, Calgary, AB, Canada disorders (ASDs). Children with autism typically have
difficulties in verbal and non-verbal communication, social
D. L. Sigalet interactions, and leisure or play activities. The prevalence
Department of Surgery, University of Calgary, Calgary, AB,
Canada of ASDs, has been estimated to be 6.6:1000 with the
prevalence of autism increasing (Blaxill 2004; Chakrabarti
J. J. Holst and Fombonne 2005; Charman 2002; Rice 2007). In most
Department of Medical Physiology, University of Copenhagen, children with autism the etiology is unknown.
Copenhagen, Denmark
Gastrointestinal symptoms are reported to be more
J. B. Meddings common in children with ASDs although this is somewhat
Department of Medicine, University of Alberta, Edmonton, AB, controversial (Molloy and Manning-Courtney 2003; Horv-
Canada
ath et al. 1999; Valicenti-McDermott et al. 2006; Kuddo
J. Wood and Nelson 2003). Many parents observe that the onset of
Gastroenterology and Nutrition, Alberta Children’s Hospital, gastrointestinal symptoms coincides with early concerns
2888 Shaganappi Trail NW, Calgary, AB, Canada T3B 6A8 about their infant’s development. These observations are
consistent with the hypothesis that gastrointestinal dys-
K. A. Sharkey
Department of Physiology and Biophysics, function may be causally related to the development of the
University of Calgary, Calgary, AB, Canada autistic phenotype in some children. In the ‘‘leaky-gut’’

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