Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders.
Chris EijsboutsTenghao ZhengNicholas A KennedyFerdinando BonfiglioCarl A AndersonLoukas MoutsianasJoanne HollidayJingchunzi ShiSuyash S Shringarpurenull nullAlexandru-Ioan Vodanull nullGianrico FarrugiaAndre FrankeMatthias HübenthalGonçalo R AbecasisMatthew ZawistowskiAnne Heidi SkogholtEivind Ness-JensenKristian HveemTõnu EskoMaris Teder-LavingAlexandra ZhernakovaMichael CamilleriGuy BoeckxstaensPeter J WhorwellRobin C SpillerGilean McVeanMauro D'AmatoLuke Jostins-DeanMiles ParkesPublished in: Nature genetics (2021)
Irritable bowel syndrome (IBS) results from disordered brain-gut interactions. Identifying susceptibility genes could highlight the underlying pathophysiological mechanisms. We designed a digestive health questionnaire for UK Biobank and combined identified cases with IBS with independent cohorts. We conducted a genome-wide association study with 53,400 cases and 433,201 controls and replicated significant associations in a 23andMe panel (205,252 cases and 1,384,055 controls). Our study identified and confirmed six genetic susceptibility loci for IBS. Implicated genes included NCAM1, CADM2, PHF2/FAM120A, DOCK9, CKAP2/TPTE2P3 and BAG6. The first four are associated with mood and anxiety disorders, expressed in the nervous system, or both. Mirroring this, we also found strong genome-wide correlation between the risk of IBS and anxiety, neuroticism and depression (rg > 0.5). Additional analyses suggested this arises due to shared pathogenic pathways rather than, for example, anxiety causing abdominal symptoms. Implicated mechanisms require further exploration to help understand the altered brain-gut interactions underlying IBS.
Keyphrases
- irritable bowel syndrome
- genome wide
- sleep quality
- dna methylation
- genome wide association study
- genome wide analysis
- copy number
- bipolar disorder
- depressive symptoms
- resting state
- white matter
- cross sectional
- healthcare
- mental health
- functional connectivity
- gene expression
- physical activity
- social media
- brain injury
- health information
- patient reported