Unknown

Dataset Information

0

Prediction of complicated disease course for children newly diagnosed with Crohn's disease: a multicentre inception cohort study.


ABSTRACT: BACKGROUND:Stricturing and penetrating complications account for substantial morbidity and health-care costs in paediatric and adult onset Crohn's disease. Validated models to predict risk for complications are not available, and the effect of treatment on risk is unknown. METHODS:We did a prospective inception cohort study of paediatric patients with newly diagnosed Crohn's disease at 28 sites in the USA and Canada. Genotypes, antimicrobial serologies, ileal gene expression, and ileal, rectal, and faecal microbiota were assessed. A competing-risk model for disease complications was derived and validated in independent groups. Propensity-score matching tested the effect of anti-tumour necrosis factor ? (TNF?) therapy exposure within 90 days of diagnosis on complication risk. FINDINGS:Between Nov 1, 2008, and June 30, 2012, we enrolled 913 patients, 78 (9%) of whom experienced Crohn's disease complications. The validated competing-risk model included age, race, disease location, and antimicrobial serologies and provided a sensitivity of 66% (95% CI 51-82) and specificity of 63% (55-71), with a negative predictive value of 95% (94-97). Patients who received early anti-TNF? therapy were less likely to have penetrating complications (hazard ratio [HR] 0·30, 95% CI 0·10-0·89; p=0·0296) but not stricturing complication (1·13, 0·51-2·51; 0·76) than were those who did not receive early anti-TNF? therapy. Ruminococcus was implicated in stricturing complications and Veillonella in penetrating complications. Ileal genes controlling extracellular matrix production were upregulated at diagnosis, and this gene signature was associated with stricturing in the risk model (HR 1·70, 95% CI 1·12-2·57; p=0·0120). When this gene signature was included, the model's specificity improved to 71%. INTERPRETATION:Our findings support the usefulness of risk stratification of paediatric patients with Crohn's disease at diagnosis, and selection of anti-TNF? therapy. FUNDING:Crohn's and Colitis Foundation of America, Cincinnati Children's Hospital Research Foundation Digestive Health Center.

SUBMITTER: Kugathasan S 

PROVIDER: S-EPMC5719489 | biostudies-literature | 2017 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

Prediction of complicated disease course for children newly diagnosed with Crohn's disease: a multicentre inception cohort study.

Kugathasan Subra S   Denson Lee A LA   Walters Thomas D TD   Kim Mi-Ok MO   Marigorta Urko M UM   Schirmer Melanie M   Mondal Kajari K   Liu Chunyan C   Griffiths Anne A   Noe Joshua D JD   Crandall Wallace V WV   Snapper Scott S   Rabizadeh Shervin S   Rosh Joel R JR   Shapiro Jason M JM   Guthery Stephen S   Mack David R DR   Kellermayer Richard R   Kappelman Michael D MD   Steiner Steven S   Moulton Dedrick E DE   Keljo David D   Cohen Stanley S   Oliva-Hemker Maria M   Heyman Melvin B MB   Otley Anthony R AR   Baker Susan S SS   Evans Jonathan S JS   Kirschner Barbara S BS   Patel Ashish S AS   Ziring David D   Trapnell Bruce C BC   Sylvester Francisco A FA   Stephens Michael C MC   Baldassano Robert N RN   Markowitz James F JF   Cho Judy J   Xavier Ramnik J RJ   Huttenhower Curtis C   Aronow Bruce J BJ   Gibson Greg G   Hyams Jeffrey S JS   Dubinsky Marla C MC  

Lancet (London, England) 20170302 10080


<h4>Background</h4>Stricturing and penetrating complications account for substantial morbidity and health-care costs in paediatric and adult onset Crohn's disease. Validated models to predict risk for complications are not available, and the effect of treatment on risk is unknown.<h4>Methods</h4>We did a prospective inception cohort study of paediatric patients with newly diagnosed Crohn's disease at 28 sites in the USA and Canada. Genotypes, antimicrobial serologies, ileal gene expression, and  ...[more]

Similar Datasets

| S-EPMC5355514 | biostudies-literature
| S-EPMC4418409 | biostudies-literature
| S-EPMC6906406 | biostudies-literature
| S-EPMC8666701 | biostudies-literature
| S-EPMC3459595 | biostudies-literature
| S-EPMC6278907 | biostudies-literature
| S-EPMC4130535 | biostudies-literature
2018-10-30 | GSE117889 | GEO
| S-EPMC4884453 | biostudies-literature
| S-EPMC8803753 | biostudies-literature