Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease.

Serra EG., Schwerd T., Moutsianas L., Cavounidis A., Fachal L., Pandey S., Kammermeier J., Croft NM., Posovszky C., Rodrigues A., Russell RK., Barakat F., Auth MKH., Heuschkel R., Zilbauer M., Fyderek K., Braegger C., Travis SP., Satsangi J., Parkes M., Thapar N., Ferry H., Matte JC., Gilmour KC., Wedrychowicz A., Sullivan P., Moore C., Sambrook J., Ouwehand W., Roberts D., Danesh J., Baeumler TA., Fulga TA., Karaminejadranjbar M., Ahmed A., Wilson R., Barrett JC., Elkadri A., Griffiths AM., COLORS in IBD group investigators None., Oxford IBD cohort study investigators None., INTERVAL Study None., Swiss IBD cohort investigators None., UK IBD Genetics Consortium None., NIDDK IBD Genetics Consortium None., Snapper SB., Shah N., Muise AM., Wilson DC., Uhlig HH., Anderson CA.

Very-early-onset inflammatory bowel disease (VEO-IBD) is a heterogeneous phenotype associated with a spectrum of rare Mendelian disorders. Here, we perform whole-exome-sequencing and genome-wide genotyping in 145 patients (median age-at-diagnosis of 3.5 years), in whom no Mendelian disorders were clinically suspected. In five patients we detect a primary immunodeficiency or enteropathy, with clinical consequences (XIAP, CYBA, SH2D1A, PCSK1). We also present a case study of a VEO-IBD patient with a mosaic de novo, pathogenic allele in CYBB. The mutation is present in ~70% of phagocytes and sufficient to result in defective bacterial handling but not life-threatening infections. Finally, we show that VEO-IBD patients have, on average, higher IBD polygenic risk scores than population controls (99 patients and 18,780 controls; P < 4 × 10-10), and replicate this finding in an independent cohort of VEO-IBD cases and controls (117 patients and 2,603 controls; P < 5 × 10-10). This discovery indicates that a polygenic component operates in VEO-IBD pathogenesis.

DOI

10.1038/s41467-019-14275-y

Type

Journal article

Journal

Nature communications

Publication Date

21/02/2020

Volume

11

Addresses

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.

Keywords

COLORS in IBD group investigators, Oxford IBD cohort study investigators, INTERVAL Study, Swiss IBD cohort investigators, UK IBD Genetics Consortium, NIDDK IBD Genetics Consortium, Humans, Inflammatory Bowel Diseases, Genetic Predisposition to Disease, Risk Factors, Case-Control Studies, Cohort Studies, Pedigree, Age of Onset, Genes, Recessive, Multifactorial Inheritance, Mutation, Mosaicism, Adult, Child, Child, Preschool, Infant, Infant, Newborn, Female, Male, Genetic Variation, Whole Exome Sequencing, Loss of Function Mutation, NADPH Oxidase 2, Primary Immunodeficiency Diseases

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