Antitumour necrosis factor therapy is associated with de novo Crohn's disease after ileal pouch-anal anastomosis.
IBD
IPAA
anti-TNF
de novo Crohn's disease
ulcerative colitis
Journal
Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland
ISSN: 1463-1318
Titre abrégé: Colorectal Dis
Pays: England
ID NLM: 100883611
Informations de publication
Date de publication:
Sep 2021
Sep 2021
Historique:
revised:
02
05
2021
received:
20
10
2020
accepted:
09
05
2021
pubmed:
23
6
2021
medline:
5
10
2021
entrez:
22
6
2021
Statut:
ppublish
Résumé
Tumour necrosis factor inhibitors (TNFi) have revolutionized the management of moderate to severe ulcerative colitis (UC) since their approval for UC in 2005. However, many patients ultimately require surgery with ileal pouch-anal anastomosis (IPAA). Development of de novo Crohn's disease (CD) following IPAA is an increasingly common and devastating complication, sometimes progressing to pouch failure. The aim of this study was to evaluate the association of preoperative TNFi exposure and the development of de novo CD after IPAA. A prospective single-centre inflammatory bowel disease (IBD) registry was searched for consecutive patients with UC undergoing IPAA during a 25-year period ending July 2018. Patients with preoperative CD or IBD-unclassified were excluded. De novo CD was diagnosed upon endoscopic evidence of five or more mucosal ulcers proximal to the ileal pouch any time after surgery and/or pouch fistula occurring more than three months after ileostomy closure. The study cohort consisted of 400 patients with a median follow-up of 44.0 (IQR 11-113) months. Sixty-two (16%) patients developed de novo CD 28.0 (IQR 6-67) months following ileostomy closure. Survival analysis of TNFi era patients revealed a significant increase in de novo CD risk in those with preoperative TNFi exposure. Multivariable proportional hazards modelling revealed two independent predictors for de novo CD development: older age was protective (HR 0.89 per 5-year increase; P = 0.009) and preoperative TNFi exposure was hazardous (HR 2.10; P = 0.011). This prospective study is the first to suggest an association between preoperative TNFi exposure and the development of de novo CD.
Identifiants
pubmed: 34157179
doi: 10.1111/codi.15772
pmc: PMC8440372
mid: NIHMS1717879
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2416-2424Subventions
Organisme : NCATS NIH HHS
ID : UL1TR001881
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK062413
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01DK062413
Pays : United States
Organisme : Widjaja Foundation Inflammatory Bowel and Immunobiology Research Institute
Organisme : NIDDK NIH HHS
ID : P01 DK046763
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001881
Pays : United States
Organisme : Leona M. and Harry B. Helmsley Charitable Trust
ID : 2014PG-IBD014
Organisme : NIDDK NIH HHS
ID : P01DK046763
Pays : United States
Informations de copyright
© 2021 The Association of Coloproctology of Great Britain and Ireland.
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