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Clinical Presentation and Histologic Findings at
Ileocolonoscopy in Children with Autistic Spectrum Disorder and Chronic
Gastrointestinal Symptoms
Authors: Arthur Krigsman, Marvin Boris, Alan Goldblatt and Carol Stott
Publication Date: 27 Jan 2010
Autism Insights 2010:2 1-11
Arthur Krigsman1, Marvin Boris2, Alan Goldblatt3 and Carol Stott4
1Assistant Professor of Pediatrics, New York University School of Medicine
Director of Gastroenterology Services, Thoughtful House Center for Children,
3001 Bee Caves Rd, Austin, Texas, 78746, USA. 2Associate Clinical Professor of
Pediatrics, New York University School of Medicine, 550 1st Ave., New York, NY
10016, USA. 3Adjunct Professor Touro College, 27-33 West 23rd St, New York, NY
10010, USA. 4Thoughtful House Center for Children, 3001 Bee Caves Rd, Austin,
Texas, 78746, USA.
Abstract
Background: Children with developmental disorders experience chronic
gastrointestinal symptoms.
Aims: To examine the nature of these gastrointestinal symptoms and histologic
findings in children with autism spectrum/developmental disorders and
ileocolonic disease.
Methods: Chart review. 143 autism spectrum/developmental disorder patients, with
chronic gastrointestinal symptoms, undergoing diagnostic ileocolonoscopy.
Results: Diarrhea was present in 78%, abdominal pain in 59% and constipation in
36%. Ileal and/or colonic lymphonodular hyperplasia (LNH), defined as the
presence of an increased number of enlarged lymphoid follicles, often with
hyperactive germinal centers, was present in 73.2%. Terminal ileum LNH presented
visually in 67% and histologically in 73%. Colonic LNH was multifocal and
presented histologically in 32%. Ileal and/or colonic inflammation presented in
74%, consisting primarily of active or chronic colitis (69%). Ileal inflammation
presented in 35%. Presence of LNH significantly predicted mucosal inflammation.
Patients with ileal and/or colonic LNH had lower mean/median age than those
without; patients with ileal and/or colonic inflammation had lower mean/median
age than those without. There was a significant association between ileo and/or
colonic inflammation or LNH, and onset of developmental disorder; plateaued or
regressive onset conferred greater risk than early onset.
Conclusions: Patients with autism or related disorders exhibiting chronic
gastrointestinal symptoms demonstrate ileal or colonic inflammation upon light
microscopic examination of biopsy tissue. Further work is needed to determine
whether resolution of histopathology with appropriate therapy is accompanied by
GI symptomatic and cognitive/behavioral improvement.
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