Identification of unique gene expression profile in children with regressive autism spectrum disorder (ASD) and ileocolitis.

Gastrointestinal symptoms are common in children with autism spectrum disorder (ASD) and are often associated with mucosal inflammatory infiltrates of the small and large intestine. Although distinct histologic and immunohistochemical properties of this inflammatory infiltrate have been previously d...

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Autores principales: Stephen J Walker, John Fortunato, Lenny G Gonzalez, Arthur Krigsman
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:d4b15115e5524d0b85d40413fe6bc6452021-11-18T07:54:12ZIdentification of unique gene expression profile in children with regressive autism spectrum disorder (ASD) and ileocolitis.1932-620310.1371/journal.pone.0058058https://doaj.org/article/d4b15115e5524d0b85d40413fe6bc6452013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23520485/?tool=EBIhttps://doaj.org/toc/1932-6203Gastrointestinal symptoms are common in children with autism spectrum disorder (ASD) and are often associated with mucosal inflammatory infiltrates of the small and large intestine. Although distinct histologic and immunohistochemical properties of this inflammatory infiltrate have been previously described in this ASD(GI) group, molecular characterization of these lesions has not been reported. In this study we utilize transcriptome profiling of gastrointestinal mucosal biopsy tissue from ASD(GI) children and three non-ASD control groups (Crohn's disease, ulcerative colitis, and histologically normal) in an effort to determine if there is a gene expression profile unique to the ASD(GI) group. Comparison of differentially expressed transcripts between the groups demonstrated that non-pathologic (normal) tissue segregated almost completely from inflamed tissue in all cases. Gene expression profiles in intestinal biopsy tissue from patients with Crohn's disease, ulcerative colitis, and ASD(GI), while having significant overlap with each other, also showed distinctive features for each group. Taken together, these results demonstrate that ASD(GI) children have a gastrointestinal mucosal molecular profile that overlaps significantly with known inflammatory bowel disease (IBD), yet has distinctive features that further supports the presence of an ASD-associated IBD variant, or, alternatively, a prodromal phase of typical inflammatory bowel disease. Although we report qPCR confirmation of representative differentially expressed transcripts determined initially by microarray, these findings may be considered preliminary to the extent that they require further confirmation in a validation cohort.Stephen J WalkerJohn FortunatoLenny G GonzalezArthur KrigsmanPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 3, p e58058 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Stephen J Walker
John Fortunato
Lenny G Gonzalez
Arthur Krigsman
Identification of unique gene expression profile in children with regressive autism spectrum disorder (ASD) and ileocolitis.
description Gastrointestinal symptoms are common in children with autism spectrum disorder (ASD) and are often associated with mucosal inflammatory infiltrates of the small and large intestine. Although distinct histologic and immunohistochemical properties of this inflammatory infiltrate have been previously described in this ASD(GI) group, molecular characterization of these lesions has not been reported. In this study we utilize transcriptome profiling of gastrointestinal mucosal biopsy tissue from ASD(GI) children and three non-ASD control groups (Crohn's disease, ulcerative colitis, and histologically normal) in an effort to determine if there is a gene expression profile unique to the ASD(GI) group. Comparison of differentially expressed transcripts between the groups demonstrated that non-pathologic (normal) tissue segregated almost completely from inflamed tissue in all cases. Gene expression profiles in intestinal biopsy tissue from patients with Crohn's disease, ulcerative colitis, and ASD(GI), while having significant overlap with each other, also showed distinctive features for each group. Taken together, these results demonstrate that ASD(GI) children have a gastrointestinal mucosal molecular profile that overlaps significantly with known inflammatory bowel disease (IBD), yet has distinctive features that further supports the presence of an ASD-associated IBD variant, or, alternatively, a prodromal phase of typical inflammatory bowel disease. Although we report qPCR confirmation of representative differentially expressed transcripts determined initially by microarray, these findings may be considered preliminary to the extent that they require further confirmation in a validation cohort.
format article
author Stephen J Walker
John Fortunato
Lenny G Gonzalez
Arthur Krigsman
author_facet Stephen J Walker
John Fortunato
Lenny G Gonzalez
Arthur Krigsman
author_sort Stephen J Walker
title Identification of unique gene expression profile in children with regressive autism spectrum disorder (ASD) and ileocolitis.
title_short Identification of unique gene expression profile in children with regressive autism spectrum disorder (ASD) and ileocolitis.
title_full Identification of unique gene expression profile in children with regressive autism spectrum disorder (ASD) and ileocolitis.
title_fullStr Identification of unique gene expression profile in children with regressive autism spectrum disorder (ASD) and ileocolitis.
title_full_unstemmed Identification of unique gene expression profile in children with regressive autism spectrum disorder (ASD) and ileocolitis.
title_sort identification of unique gene expression profile in children with regressive autism spectrum disorder (asd) and ileocolitis.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/d4b15115e5524d0b85d40413fe6bc645
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AT lennyggonzalez identificationofuniquegeneexpressionprofileinchildrenwithregressiveautismspectrumdisorderasdandileocolitis
AT arthurkrigsman identificationofuniquegeneexpressionprofileinchildrenwithregressiveautismspectrumdisorderasdandileocolitis
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