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PMID: 22837873 Published · ppublish English Journal Article

An Update on Post-infectious Irritable Bowel Syndrome: Role of Genetics, Immune Activation, Serotonin and Altered Microbiome.

Journal of neurogastroenterology and motility ·Vol. 18 ·No. 3 ·2012-07-00 ·Pages 258-68

Spiller R, Lam C

Abstract

The literature on post-infectious irritable bowel syndrome (IBS) is reviewed with special emphasis on recent new data. Further accounts of this phenomenon continue to be reported following a range of infections including giardiasis as well as viral and bacterial gastroenteritis. Risk factors such as severity of initial illness, female gender together with adverse psychological factors have been confirmed. Recent evidence of a genetic predisposition needs replication. Animal studies suggest activation of mast cells and inflammation driven impairment of serotonin transporter may be important, which are findings supported by some recent human studies in IBS with diarrhoea. Experimentally induced inflammation leads to damage and remodelling of enteric nerves. Similar changes have been reported in IBS patients with increase in nerves expressing transient receptor potential cation channel V1. While changes in microbiota are very likely this area has yet to be explored using modern techniques. Since the prognosis is for slow improvement, treatments should currently target the key symptoms of diarrhoea and abdominal pain. Future therapies aimed at correcting underlying mechanisms including immune activation and serotonin excess are currently being explored and may provide better treatments in the future.

Keywords
Genetics Infection Irritable bowel syndrome Serotonin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Spiller Robin
NIHR Biomedical Research Unit in the Nottingham Digestive Diseases Centre, Nottingham, United Kingdom.
Lam Ching
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Article Info
Journal
Journal of neurogastroenterology and motility
Abbr.
J Neurogastroenterol Motil
ISSN
2093-0887
Published
2012-07-00
Epub
2012-00-10
Pages
258-68
Language
English
Region
Korea (South)
NLM ID
101530189
PMCID
PMC3400813
Grants
Medical Research Council · MC_G1002464 · United Kingdom
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