Abnormal Liver Biochemistry Is Common in Pediatric Inflammatory Bowel Disease: Prevalence and Associations. Issue 12 (December 2015)
- Record Type:
- Journal Article
- Title:
- Abnormal Liver Biochemistry Is Common in Pediatric Inflammatory Bowel Disease: Prevalence and Associations. Issue 12 (December 2015)
- Main Title:
- Abnormal Liver Biochemistry Is Common in Pediatric Inflammatory Bowel Disease
- Authors:
- Valentino, Pamela L.
Feldman, Brian M.
Walters, Thomas D.
Griffiths, Anne M.
Ling, Simon C.
Pullenayegum, Eleanor M.
Kamath, Binita M. - Abstract:
- Abstract : Background: Liver enzymes (LEs) abnormalities associated with pediatric inflammatory bowel diseases (IBD) are understudied. We undertook to describe the development and associations of abnormal LEs in pediatric IBD. Methods: We ascertained a cohort of 300 children with IBD and collected retrospective data. A Kaplan–Meier analysis determined the time to development of different thresholds of abnormal LEs. Associations between clinical variables and the development of abnormal LEs were determined. Results: The probability of developing the first episode of abnormal LEs above the upper limit of normal (ULN) within 150 months was 58.1% (16.3% by 1 mo post-IBD diagnosis). There was a 6% prevalence of primary sclerosing cholangitis (PSC) or autoimmune sclerosing cholangitis (ASC) in this cohort. Of those diagnosed with PSC/ASC, 93% had persistent LE elevations at a threshold of >2× ULN, while those without PSC/ASC had a 4% probability of this abnormality. Elevated gamma glutamyltranspeptidase levels of 252 U/L had a 99% sensitivity and 71% specificity for PSC/ASC in IBD. After exclusion of patients with PSC/ASC, corticosteroids, antibiotics, and exclusive enteral nutrition demonstrated strongly positive associations with the first development of abnormal LEs >ULN (hazard ratio 2.1 [95% confidence interval, 1.3–3.3], hazard ratio 5.6 [95% confidence interval, 3.6–8.9], hazard ratio 4.2 [95% confidence interval, 1.6–11.3], respectively). Conclusions: Abnormal LEs areAbstract : Background: Liver enzymes (LEs) abnormalities associated with pediatric inflammatory bowel diseases (IBD) are understudied. We undertook to describe the development and associations of abnormal LEs in pediatric IBD. Methods: We ascertained a cohort of 300 children with IBD and collected retrospective data. A Kaplan–Meier analysis determined the time to development of different thresholds of abnormal LEs. Associations between clinical variables and the development of abnormal LEs were determined. Results: The probability of developing the first episode of abnormal LEs above the upper limit of normal (ULN) within 150 months was 58.1% (16.3% by 1 mo post-IBD diagnosis). There was a 6% prevalence of primary sclerosing cholangitis (PSC) or autoimmune sclerosing cholangitis (ASC) in this cohort. Of those diagnosed with PSC/ASC, 93% had persistent LE elevations at a threshold of >2× ULN, while those without PSC/ASC had a 4% probability of this abnormality. Elevated gamma glutamyltranspeptidase levels of 252 U/L had a 99% sensitivity and 71% specificity for PSC/ASC in IBD. After exclusion of patients with PSC/ASC, corticosteroids, antibiotics, and exclusive enteral nutrition demonstrated strongly positive associations with the first development of abnormal LEs >ULN (hazard ratio 2.1 [95% confidence interval, 1.3–3.3], hazard ratio 5.6 [95% confidence interval, 3.6–8.9], hazard ratio 4.2 [95% confidence interval, 1.6–11.3], respectively). Conclusions: Abnormal LEs are common in pediatric IBD and occur early. PSC/ASC is associated with persistently high LEs and gamma glutamyltranspeptidase levels >252 U/L. Children with IBD are at risk of elevated LEs if they require medications other than 5-ASA to induce IBD remission. Abstract : Article first published online 13 August 2015.Supplemental Digital Content is Available in the Text. … (more)
- Is Part Of:
- Inflammatory bowel diseases. Volume 21:Issue 12(2015:Dec.)
- Journal:
- Inflammatory bowel diseases
- Issue:
- Volume 21:Issue 12(2015:Dec.)
- Issue Display:
- Volume 21, Issue 12 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 12
- Issue Sort Value:
- 2015-0021-0012-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-12
- Subjects:
- inflammatory bowel diseases -- primary sclerosing cholangitis -- autoimmune sclerosing cholangitis -- liver enzymes
Inflammatory bowel diseases -- Periodicals
Colitis, Ulcerative -- Periodicals
Crohn Disease -- Periodicals
Inflammatory Bowel Diseases -- Periodicals
616.344 - Journal URLs:
- http://journals.lww.com/ibdjournal/pages/default.aspx ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1536-4844/ ↗
http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=ovft&AN=00054725-000000000-00000 ↗
https://academic.oup.com/ibdjournal ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/MIB.0000000000000558 ↗
- Languages:
- English
- ISSNs:
- 1078-0998
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4478.845400
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5190.xml