Genetics of irritable bowel syndrome

Maria Henström, Mauro D'Amato

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Irritable bowel syndrome (IBS) is a common condition with a complex and largely unknown etiology. There is no cure, and treatment options are mainly directed to the amelioration of symptoms. IBS causes reduced quality of life and poses considerable repercussions on health and socioeconomic systems. There is a heritable component in IBS, and genetic research is a valuable tool for the identification of causative pathways, which will provide important insight into the pathophysiology. However, although some gene-hunting efforts have been conducted and a few risk genes proposed, IBS genetic research is lagging behind compared to other complex diseases. In this mini-review, we briefly summarize existing genetic studies, discuss the main challenges in IBS genetic research, and propose strategies to overcome these challenges for IBS gene discovery.
Original languageEnglish
Article number7
Number of pages5
JournalMolecular and Cellular Pediatrics
Volume3
DOIs
Publication statusPublished - 2016
Externally publishedYes

Keywords

  • Genetics
  • Genome-wide association study
  • Irritable bowel syndrome

Cite this