| Title: | Rome III criteria capture higher irritable bowel syndrome SNP-heritability and highlight a novel genetic link with cardiovascular traits |
| Journal: | Cellular and Molecular Gastroenterology and Hepatology |
| Published: | 18 Apr 2024 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/38643935/ |
| DOI: | https://doi.org/10.1016/j.jcmgh.2024.04.002 |
| URL: | http://dx.doi.org/10.1016/j.jcmgh.2024.04.002 |
Publication 9864
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Abstract
BACKGROUND & AIMS: Irritable bowel syndrome (IBS) shows genetic predisposition, and large-scale genome-wide association studies (GWAS) are emerging, based on heterogeneous disease definitions. We aimed at investigating the genetic architecture of IBS defined according to gold-standard Rome Criteria.</p>
METHODS: We conducted GWAS meta-analyses of Rome III IBS and its subtypes in 24,735 IBS cases and 77,149 asymptomatic controls from two independent European cohorts (UK Biobank and Lifelines). SNP-based heritability (h2SNP) and genetic correlations (rg) with other traits were calculated. IBS risk loci were functionally annotated to identify candidate genes. Sensitivity and conditional analyses were conducted to assess impact of confounders. Polygenic risk scores (PRS) were computed and tested in independent datasets.</p>
RESULTS: Rome III IBS showed significant SNP-heritability (up to 13%) and similar genetic architecture across subtypes, including those with manifestations at the opposite ends of the symptom spectrum (rg=0.48 between IBS-D and IBS-C). Genetic correlations with other traits highlighted commonalities with family history of heart disease and hypertension, coronary artery disease, and angina pectoris (rg=0.20-0.45), among others. Four independent GWAS signals (p<5×10-8) were detected, including two novel loci for IBS (rs2035380) and IBS-Mixed (rs2048419) that had been previously associated with hypertension and coronary artery disease. Functional annotation of GWAS risk loci revealed genes implicated in circadian rhythm (BMAL1), intestinal barrier (CLDN23), immunomodulation (MFHAS1), and the cAMP pathway (ADCY2). PRS allowed the identification of individuals at increased risk of IBS (OR=1.34, p=1.1×10-3).</p>
CONCLUSIONS: Rome III Criteria capture higher SNP-heritability than previously estimated for IBS. The identified link between IBS and cardiovascular traits may contribute to the delineation of alternative therapeutic strategies, warranting further investigation.</p>
9 Authors
- Leticia Camargo Tavares
- Esteban Alexander Lopera-Maya
- Ferdinando Bonfiglio
- Tenghao Zheng
- Trishla Sinha
- Francine Zanchetta Marques
- Alexandra Zhernakova
- Serena Sanna
- Mauro D'Amato
1 Application
| Application ID | Title |
|---|---|
| 17435 | Exploring the genetics of irritable bowel syndrome: the ?bellygenes? initiative (project approved by bbmri-lpc) |
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