Literature DB >> 19297006

A paucity of colonic enteroendocrine and/or enterochromaffin cells characterizes a subset of patients with chronic unexplained diarrhea/malabsorption.

Steven Ohsie1, Garrett Gerney, Dorina Gui, Doron Kahana, Martín G Martín, Galen Cortina.   

Abstract

A generalized absence of enteroendocrine cells characterizes 2 diarrheal/malabsorptive diseases, namely, enteroendocrine cell dysgenesis and autoimmune polyglandular syndrome 1. However, it is not routine for pathologists to examine mucosal biopsies for enteroendocrine cells in cases of chronic diarrheal illness. Our primary aim was to prospectively examine colonic mucosa for loss of enteroendocrine cells using chromogranin A immunohistochemistry for diagnostic purposes. Our secondary aim was to investigate enterochromaffin cells as a subset of enteroendocrine cells, using serotonin (5HT) immunohistochemistry; we hypothesized that other causes of diarrhea due to loss of enteroendocrine cell subsets are missed by evaluating enteroendocrine cells alone. Our approach was limited to patients with chronic unexplained diarrhea partly selected by referring physicians who considered the patients problematic. Seven problematic patients with reduced enteroendocrine or enterochromaffin cells were collected over a 9-month period and placed in group A. Three group A patients demonstrated reduced enteroendocrine cells relative to controls, and they were later diagnosed as having enteroendocrine cell dysgenesis (n = 1) and autoimmune polyglandular syndrome 1 (n = 2). Four group A patients had reduced enterochromaffin cells but normal enteroendocrine cells. These 4 patients had conditions such as congenital diarrhea, mild graft-versus-host disease, acquired childhood chronic diarrhea, and diarrhea post lung transplant. The reduced enterochromaffin cells in the graft-versus-host disease patient inspired a third aim, that is, to investigate whether a loss of enterochromaffin cells would be a generalized defect seen in patients with mild colonic graft-versus-host disease (group B). However, no loss of enterochromaffin cells was detected in group B. Two methods of enumerating endocrine cells were used and demonstrated 67% agreement.

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Year:  2009        PMID: 19297006     DOI: 10.1016/j.humpath.2008.12.016

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  8 in total

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Journal:  Am J Gastroenterol       Date:  2011-12-13       Impact factor: 10.864

2.  APECED: is this a model for failure of T cell and B cell tolerance?

Authors:  Nicolas Kluger; Annamari Ranki; Kai Krohn
Journal:  Front Immunol       Date:  2012-08-02       Impact factor: 7.561

3.  The Basic Helix-Loop-Helix Transcription Factor NEUROG3 Is Required for Development of the Human Endocrine Pancreas.

Authors:  Patrick S McGrath; Carey L Watson; Cameron Ingram; Michael A Helmrath; James M Wells
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4.  Neurogenin 3 is important but not essential for pancreatic islet development in humans.

Authors:  Oscar Rubio-Cabezas; Ethel Codner; Sarah E Flanagan; José L Gómez; Sian Ellard; Andrew T Hattersley
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Review 5.  Understanding inborn errors of immunity: A lens into the pathophysiology of monogenic inflammatory bowel disease.

Authors:  Jodie Deborah Ouahed
Journal:  Front Immunol       Date:  2022-09-29       Impact factor: 8.786

6.  Dysgenesis of enteroendocrine cells in Aristaless-Related Homeobox polyalanine expansion mutations.

Authors:  Natalie A Terry; Randall A Lee; Erik R Walp; Klaus H Kaestner; Catherine Lee May
Journal:  J Pediatr Gastroenterol Nutr       Date:  2015-02       Impact factor: 2.839

7.  Identification of novel, clinically correlated autoantigens in the monogenic autoimmune syndrome APS1 by proteome-wide PhIP-Seq.

Authors:  Joseph L DeRisi; Mark S Anderson; Sara E Vazquez; Elise Mn Ferré; David W Scheel; Sara Sunshine; Brenda Miao; Caleigh Mandel-Brehm; Zoe Quandt; Alice Y Chan; Mickie Cheng; Michael German; Michail Lionakis
Journal:  Elife       Date:  2020-05-15       Impact factor: 8.140

8.  Novel Homozygous Inactivating Mutation in the PCSK1 Gene in an Infant with Congenital Malabsorptive Diarrhea.

Authors:  Laetitia Aerts; Nathalie A Terry; Nina N Sainath; Clarivet Torres; Martín G Martín; Bruno Ramos-Molina; John W Creemers
Journal:  Genes (Basel)       Date:  2021-05-10       Impact factor: 4.096

  8 in total

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