• norsk
    • English
  • English 
    • norsk
    • English
  • Login
View Item 
  •   Home
  • Fakultet for helsevitenskap (HV)
  • HV - Institutt for sykepleie og helsefremmende arbeid
  • View Item
  •   Home
  • Fakultet for helsevitenskap (HV)
  • HV - Institutt for sykepleie og helsefremmende arbeid
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Serological markers in diagnosis of pediatric inflammatory bowel disease and as predictors for early tumor necrosis factor blocker therapy

Olbjørn, Christine; Småstuen, Milada Cvancarova; Thiis-Evensen, Espen; Nakstad, Britt; Vatn, Morten H; Perminow, Gøri Margrete
Journal article, Peer reviewed
Accepted version
Thumbnail
View/Open
Artikkel_serologi_revised_final_SJG_021116.pdf (156.3Kb)
URI
https://hdl.handle.net/10642/6546
Date
2016-11-25
Metadata
Show full item record
Collections
  • HV - Institutt for sykepleie og helsefremmende arbeid [1566]
Original version
Olbjørn C, Småstuen MC, Thiis-Evensen E, Nakstad B, Vatn MH, Perminow GM. Serological markers in diagnosis of pediatric inflammatory bowel disease and as predictors for early tumor necrosis factor blocker therapy. Scandinavian Journal of Gastroenterology. 2017;52(4):414-419   http://dx.doi.org/10.1080/00365521.2016.1259653
Abstract
Objective: To describe the prevalence of serological markers in newly diagnosed treatment

naïve pediatric inflammatory bowel disease (IBD), their utility in differentiating Crohn’s

disease (CD), ulcerative colitis (UC) and symptomatic non-IBD patients and whether

serological markers are associated with early TNF blocker treatment.

Material and methods: Ninety-six children and adolescents < 18 years, 58 with IBD and 38

symptomatic non-IBD controls were included. At diagnosis and after 1-2 years, serological

antibodies (anti–Saccharomyces cerevisiae antibodies (ASCA), perinuclear anti-neutrophil

cytoplasmic antibody (pANCA), flagellin expressed by Clostridial phylum (anti-CBir), outer

membrane porin of Escherichia coli (anti-OmpC), Pseudomonas fluorescens associated

sequence (anti-I2)), CRP, ESR, and fecal calprotectin were analyzed. The choice of treatment

was made at the discretion of the treating pediatrician.

Results: Of the IBD patients 20 (36%) and 26 (47%) were positive for ASCA and pANCA

compared to 3(8%), p<0.01 and 10 (27%), p=0.04 of the controls. Thirteen (72%) of UC

patients were pANCA positive, versus 13 (35%) of CD patients (p<0.01). None of the UC

patients was ASCA positive versus 20 (54%) of CD patients (p<0.0001). Compared to

conventionally treated patients, the 18 (49%) TNF blocker treated CD patients had higher

presence of ASCA (p<0.01) lower presence of pANCA (p=0.02) and higher levels of fecal

calprotectin, CRP and ESR at diagnosis. In multivariate analyses ASCA and pANCA status,

but not CRP, ESR or calprotectin, were independently associated with early TNF blocker

treatment.

Conclusions: ASCA and pANCA status were associated with having IBD and with early

TNF blocker treatment in CD.
Publisher
Taylor and Francis
Series
Scandinavian Journal of Gastroenterology;Volume 52, 2017 - Issue 4
Journal
Scandinavian Journal of Gastroenterology

Contact Us | Send Feedback

Privacy policy
DSpace software copyright © 2002-2019  DuraSpace

Service from  Unit
 

 

Browse

ArchiveCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsDocument TypesJournalsThis CollectionBy Issue DateAuthorsTitlesSubjectsDocument TypesJournals

My Account

Login

Statistics

View Usage Statistics

Contact Us | Send Feedback

Privacy policy
DSpace software copyright © 2002-2019  DuraSpace

Service from  Unit