A GWAS meta-analysis from 5 population-based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome

F. Bonfiglio, M. Henstrom, A. Nag, F. Hadizadeh, T. Zheng, M. C. Cenit, E. Tigchelaar, F. Williams, A. Reznichenko, W. E. Ek, N. V. Rivera, G. Homuth, A. A. Aghdassi, T. Kacprowski, M. Mannikko, V. Karhunen, L. Bujanda, J. Rafter, C. Wijmenga, J. RonkainenP. Hysi, A. Zhernakova, M. D'Amato*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

14 Citations (Scopus)

Abstract

BackgroundIrritable bowel syndrome (IBS) shows genetic predisposition, however, large-scale, powered gene mapping studies are lacking. We sought to exploit existing genetic (genotype) and epidemiological (questionnaire) data from a series of population-based cohorts for IBS genome-wide association studies (GWAS) and their meta-analysis.

MethodsBased on questionnaire data compatible with Rome III Criteria, we identified a total of 1335 IBS cases and 9768 asymptomatic individuals from 5 independent European genotyped cohorts. Individual GWAS were carried out with sex-adjusted logistic regression under an additive model, followed by meta-analysis using the inverse variance method. Functional annotation of significant results was obtained via a computational pipeline exploiting ontology and interaction networks, and tissue-specific and gene set enrichment analyses.

Key ResultsSuggestive GWAS signals (P5.0x10(-6)) were detected for 7 genomic regions, harboring 64 gene candidates to affect IBS risk via functional or expression changes. Functional annotation of this gene set convincingly (best FDR-corrected P=3.1x10(-10)) highlighted regulation of ion channel activity as the most plausible pathway affecting IBS risk.

Conclusion & InferencesOur results confirm the feasibility of population-based studies for gene-discovery efforts in IBS, identify risk genes and loci to be prioritized in independent follow-ups, and pinpoint ion channels as important players and potential therapeutic targets warranting further investigation.

Original languageEnglish
Article number13358
Number of pages11
JournalNeurogastroenterology and motility
Volume30
Issue number9
DOIs
Publication statusPublished - Sep-2018

Keywords

  • IBS
  • SNP
  • genetics
  • GWAS
  • meta-analysis
  • GENOME-WIDE ASSOCIATION
  • FUNCTIONAL GI DISORDERS
  • SWEDISH TWIN REGISTRY
  • GASTROINTESTINAL DISORDERS
  • BRUGADA-SYNDROME
  • QUALITY-CONTROL
  • TRP CHANNELS
  • EXPRESSION
  • POLYMORPHISMS

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