Systematic review: the role of bile acids in the pathogenesis of gastro‐oesophageal reflux disease and related neoplasia

Aliment Pharmacol Ther 2011; 34: 146–165 Summary Background  Factors other than acid may play a role in gastro‐oesophageal reflux disease (GERD) and its complications. Aim  To assessed the role of bile acids in the pathogenesis of GERD, Barrett’s oesophagus and Barrett’s‐related neoplasia. Methods ...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2011-07, Vol.34 (2), p.146-165
Hauptverfasser: McQuaid, K. R., Laine, L., Fennerty, M. B., Souza, R., Spechler, S. J.
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container_issue 2
container_start_page 146
container_title Alimentary pharmacology & therapeutics
container_volume 34
creator McQuaid, K. R.
Laine, L.
Fennerty, M. B.
Souza, R.
Spechler, S. J.
description Aliment Pharmacol Ther 2011; 34: 146–165 Summary Background  Factors other than acid may play a role in gastro‐oesophageal reflux disease (GERD) and its complications. Aim  To assessed the role of bile acids in the pathogenesis of GERD, Barrett’s oesophagus and Barrett’s‐related neoplasia. Methods  We conducted a systematic review of computerised bibliographic databases for original articles involving humans or human oesophageal tissue or cells that assessed exposure to or manipulation of bile acids. Outcomes assessed included GERD symptoms; gross oesophageal injury; Barrett’s oesophagus and related neoplasia; and intermediate markers of inflammation, proliferation or neoplasia. Results  Eighty‐three original articles were included. In in vivo studies, bile acids concentrations were higher in the oesophageal aspirates of patients with GERD than controls, and bile acids infusions triggered GERD symptoms, especially in high concentrations or in combination with acid. In ex vivo/in vitro studies, bile acids stimulated squamous oesophageal cells and Barrett’s epithelial cells to produce inflammatory mediators (e.g., IL‐8 and COX‐2) and caused oxidative stress, DNA damage and apoptosis. They also induced squamous cells to change their gene expression pattern to resemble intestinal‐type cells and caused Barrett’s cells to increase expression of intestinal‐type genes. Conclusions  In aggregate, these studies suggest that bile acids may contribute to the pathogenesis of symptoms, oesophagitis and Barrett’s metaplasia with related carcinogenesis in patients with GERD. However, all study results are not uniform and substantial differences in study parameters may explain at least some of this variation.
doi_str_mv 10.1111/j.1365-2036.2011.04709.x
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R. ; Laine, L. ; Fennerty, M. B. ; Souza, R. ; Spechler, S. J.</creator><creatorcontrib>McQuaid, K. R. ; Laine, L. ; Fennerty, M. B. ; Souza, R. ; Spechler, S. J.</creatorcontrib><description>Aliment Pharmacol Ther 2011; 34: 146–165 Summary Background  Factors other than acid may play a role in gastro‐oesophageal reflux disease (GERD) and its complications. Aim  To assessed the role of bile acids in the pathogenesis of GERD, Barrett’s oesophagus and Barrett’s‐related neoplasia. Methods  We conducted a systematic review of computerised bibliographic databases for original articles involving humans or human oesophageal tissue or cells that assessed exposure to or manipulation of bile acids. Outcomes assessed included GERD symptoms; gross oesophageal injury; Barrett’s oesophagus and related neoplasia; and intermediate markers of inflammation, proliferation or neoplasia. Results  Eighty‐three original articles were included. In in vivo studies, bile acids concentrations were higher in the oesophageal aspirates of patients with GERD than controls, and bile acids infusions triggered GERD symptoms, especially in high concentrations or in combination with acid. In ex vivo/in vitro studies, bile acids stimulated squamous oesophageal cells and Barrett’s epithelial cells to produce inflammatory mediators (e.g., IL‐8 and COX‐2) and caused oxidative stress, DNA damage and apoptosis. They also induced squamous cells to change their gene expression pattern to resemble intestinal‐type cells and caused Barrett’s cells to increase expression of intestinal‐type genes. Conclusions  In aggregate, these studies suggest that bile acids may contribute to the pathogenesis of symptoms, oesophagitis and Barrett’s metaplasia with related carcinogenesis in patients with GERD. However, all study results are not uniform and substantial differences in study parameters may explain at least some of this variation.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/j.1365-2036.2011.04709.x</identifier><identifier>PMID: 21615439</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Barrett Esophagus - etiology ; Bile Acids and Salts - physiology ; Biological and medical sciences ; Digestive system ; Esophageal Neoplasms - etiology ; Esophagus ; Gastric Emptying - physiology ; Gastroenterology. Liver. Pancreas. Abdomen ; Gastroesophageal Reflux - etiology ; Humans ; Hydrogen-Ion Concentration ; Medical sciences ; Other diseases. Semiology ; Pharmacology. 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R.</creatorcontrib><creatorcontrib>Laine, L.</creatorcontrib><creatorcontrib>Fennerty, M. B.</creatorcontrib><creatorcontrib>Souza, R.</creatorcontrib><creatorcontrib>Spechler, S. J.</creatorcontrib><title>Systematic review: the role of bile acids in the pathogenesis of gastro‐oesophageal reflux disease and related neoplasia</title><title>Alimentary pharmacology &amp; therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Aliment Pharmacol Ther 2011; 34: 146–165 Summary Background  Factors other than acid may play a role in gastro‐oesophageal reflux disease (GERD) and its complications. Aim  To assessed the role of bile acids in the pathogenesis of GERD, Barrett’s oesophagus and Barrett’s‐related neoplasia. Methods  We conducted a systematic review of computerised bibliographic databases for original articles involving humans or human oesophageal tissue or cells that assessed exposure to or manipulation of bile acids. Outcomes assessed included GERD symptoms; gross oesophageal injury; Barrett’s oesophagus and related neoplasia; and intermediate markers of inflammation, proliferation or neoplasia. Results  Eighty‐three original articles were included. In in vivo studies, bile acids concentrations were higher in the oesophageal aspirates of patients with GERD than controls, and bile acids infusions triggered GERD symptoms, especially in high concentrations or in combination with acid. In ex vivo/in vitro studies, bile acids stimulated squamous oesophageal cells and Barrett’s epithelial cells to produce inflammatory mediators (e.g., IL‐8 and COX‐2) and caused oxidative stress, DNA damage and apoptosis. They also induced squamous cells to change their gene expression pattern to resemble intestinal‐type cells and caused Barrett’s cells to increase expression of intestinal‐type genes. Conclusions  In aggregate, these studies suggest that bile acids may contribute to the pathogenesis of symptoms, oesophagitis and Barrett’s metaplasia with related carcinogenesis in patients with GERD. However, all study results are not uniform and substantial differences in study parameters may explain at least some of this variation.</description><subject>Barrett Esophagus - etiology</subject><subject>Bile Acids and Salts - physiology</subject><subject>Biological and medical sciences</subject><subject>Digestive system</subject><subject>Esophageal Neoplasms - etiology</subject><subject>Esophagus</subject><subject>Gastric Emptying - physiology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gastroesophageal Reflux - etiology</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Pharmacology. 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R.</creatorcontrib><creatorcontrib>Laine, L.</creatorcontrib><creatorcontrib>Fennerty, M. B.</creatorcontrib><creatorcontrib>Souza, R.</creatorcontrib><creatorcontrib>Spechler, S. J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McQuaid, K. R.</au><au>Laine, L.</au><au>Fennerty, M. B.</au><au>Souza, R.</au><au>Spechler, S. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systematic review: the role of bile acids in the pathogenesis of gastro‐oesophageal reflux disease and related neoplasia</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2011-07</date><risdate>2011</risdate><volume>34</volume><issue>2</issue><spage>146</spage><epage>165</epage><pages>146-165</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>Aliment Pharmacol Ther 2011; 34: 146–165 Summary Background  Factors other than acid may play a role in gastro‐oesophageal reflux disease (GERD) and its complications. Aim  To assessed the role of bile acids in the pathogenesis of GERD, Barrett’s oesophagus and Barrett’s‐related neoplasia. 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They also induced squamous cells to change their gene expression pattern to resemble intestinal‐type cells and caused Barrett’s cells to increase expression of intestinal‐type genes. Conclusions  In aggregate, these studies suggest that bile acids may contribute to the pathogenesis of symptoms, oesophagitis and Barrett’s metaplasia with related carcinogenesis in patients with GERD. However, all study results are not uniform and substantial differences in study parameters may explain at least some of this variation.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21615439</pmid><doi>10.1111/j.1365-2036.2011.04709.x</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record>
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subjects Barrett Esophagus - etiology
Bile Acids and Salts - physiology
Biological and medical sciences
Digestive system
Esophageal Neoplasms - etiology
Esophagus
Gastric Emptying - physiology
Gastroenterology. Liver. Pancreas. Abdomen
Gastroesophageal Reflux - etiology
Humans
Hydrogen-Ion Concentration
Medical sciences
Other diseases. Semiology
Pharmacology. Drug treatments
title Systematic review: the role of bile acids in the pathogenesis of gastro‐oesophageal reflux disease and related neoplasia
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