Background:It is important to identify patients with monogenic IBD as management may differ from classical IBD. In this position statement we formulate recommendations for the use of genomics in evaluating potential monogenic causes of IBD across age groups.Methods:The consensus included paediatric IBD specialists from the Paediatric IBD Porto group of the European Society of Paediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) and specialists from several monogenic IBD research consortia. We defined key topics and performed a systematic literature review to cover indications, technologies (targeted panel, exome and genome sequencing), gene panel setup, cost-effectiveness of genetic screening, and requirements for the clinical care setting. We developed recommendations that were voted upon by all authors and Porto group members (32 voting specialists).Results:We recommend next-generation DNA-sequencing technologies to diagnose monogenic causes of IBD in routine clinical practice embedded in a setting of multidisciplinary patient care. Routine genetic screening is not recommended for all IBD patients. Genetic testing should be considered depending on age of IBD-onset (infantile IBD, very early-onset IBD, paediatric or young adult IBD), and further criteria, such as family history, relevant comorbidities, and extraintestinal manifestations. Genetic testing is also recommended in advance of hematopoietic stem cell transplantation. We developed a diagnostic algorithm that includes a gene panel of 75 monogenic IBD genes. Considerations are provided also for low resource countries.Conclusions:Genomic technologies should be considered an integral part of patient care to investigate patients at risk for monogenic forms of IBD.
|Original language||American English|
|Number of pages||18|
|Journal||Journal of Pediatric Gastroenterology and Nutrition|
|State||Published - 1 Mar 2021|
Bibliographical noteFunding Information:
The Genius group and the COLORS in IBD project were supported via ESPGHAN network grants (F.M.R., H.H.U., and D.W.). H.H.U., and S.T. are funded by the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC). R.K.R. is supported by an NHS Research Scotland Career Researcher Clinician award. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. H.H.U., S.S., C.K., A.M. are supported by the Leona M. and Harry B. Helmsley Charitable Trust (VEO-IBD consortium).
© 2021 Lippincott Williams and Wilkins. All rights reserved.
- Crohn's disease
- exome sequencing
- primary immunodeficiency
- ulcerative colitis
- very early-onset inflammatory bowel disease