Publication

Presentation and disease course in early-compared to later-onset pediatric Cohn's disease

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Last modified
  • 05/14/2025
Type of Material
Authors
    Neera Gupta, University of California, San FranciscoAlan G. Bostrom, University of California, San FranciscoBarbara S. Kirschner, University of ChicagoStanley Cohen, Emory UniversityOren Abramson, Kaiser Permanente of Northern CaliforniaGeorge D. Ferry, Texas Children’s HospitalBenjamin D. Gold, Children's Healthcare AtlantaHarland S. Winter, MassGeneral Hospital for ChildrenRobert N. Baldassano, Children's Hospital of PhiladelphiaTerry Smith, Texas Children’s HospitalMelvin B. Heyman, University of California, San Francisco
Language
  • English
Date
  • 2008-08-01
Publisher
  • Springer Nature [academic journals on nature.com]: Hybrid Journals - CC BY-NC-ND or CC-NC-SA, CC BY on request
Publication Version
Copyright Statement
  • © 2008 by Am. Coll. of Gastroenterology.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0002-9270
Volume
  • 103
Issue
  • 8
Start Page
  • 2092
End Page
  • 2098
Grant/Funding Information
  • This study was supported by grants from the National Institutes of Health DK077734 (N.G.), DK060617 (M.B.H.), DK53708 (B.D.G.), DK007762 (M.B.H./N.G.); the Children’s Digestive Health and Nutrition Foundation/Crohn’s and Colitis Foundation of America Award for New Investigators (N.G.); the Crohn’s and Colitis Foundation of America Career Development Award (N.G.); and the Crohn’s and Colitis Foundation of America.
Abstract
  • BACKGROUND: The relationship between the age at diagnosis and disease course is poorly defined in children with Crohn's disease (CD). We examined the presentation and course of disease in patients 0-5 compared to 6-17 yr of age at diagnosis. METHODS: We analyzed uniform data from 989 consecutive CD patients collected between January 2000 and November 2003, and stored in the Pediatric IBD Consortium Registry. The statistical tests account for the length of follow-up of each patient. RESULTS: In total, 98 patients (9.9%) were of 0-5 yr of age at diagnosis. The mean follow-up time was 5.6 ± 5.0 yr in the younger group and 3.3 ± 2.8 yr in the older group (P < 0.001). Race/ethnicity differed by the age group (P = 0.015); a larger proportion of the younger group was Asian/Pacific Islander or Hispanic, and a larger proportion of the older group was African American. The initial classification as ulcerative colitis or indeterminate colitis was more common among the 0-5 yr of age group (P < 0.001). The 6-17 yr of age patients presented with more abdominal pain (P < 0.001), weight loss (P = 0.001), or fever (P = 0.07), while the 0-5 yr of age patients presented with more rectal bleeding (P = 0.008). The 6-17 yr of age patients were more likely to be treated with antibiotics (P < 0.001), 6-mercaptopurine/azathioprine (P < 0.001), infliximab (P = 0.001), or corticosteroids (P = 0.0006). The 6-17 yr of age patients had a higher cumulative incidence of treatment with 5-aminosalicylates (P = 0.009) or methotrexate (P = 0.04). The risk for developing an abscess (P = 0.001), a fistula (P = 0.02), a stricture (P = 0.05), or a perianal fissure (P = 0.06) was greater in the 6-17 yr of age patients. CONCLUSIONS: The 6-17 yr of age patients with CD appear to have a more complicated disease course compared to 0-5 yr of age children. The 0-5 yr of age group may represent a unique disease phenotype and benefit from different approaches to management. Long-term prospective studies are required to validate these findings.
Author Notes
  • Neera Gupta, M.D., M.A.S., UCSF Children’s Hospital, University of California, San Francisco, 500 Parnassus Avenue, MU-4 East, Box 0136, San Francisco, CA 94143-0136.
Keywords
Research Categories
  • Health Sciences, Medicine and Surgery

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