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Measurement of fecal calprotectin improves monitoring and detection of recurrence of Crohn's disease after surgery.
Wright, Emily K; Kamm, Michael A; De Cruz, Peter; Hamilton, Amy L; Ritchie, Kathryn J; Krejany, Efrosinia O; Leach, Steven; Gorelik, Alexandra; Liew, Danny; Prideaux, Lani; Lawrance, Ian C; Andrews, Jane M; Bampton, Peter A; Jakobovits, Simon L; Florin, Timothy H; Gibson, Peter R; Debinski, Henry; Macrae, Finlay A; Samuel, Douglas; Kronborg, Ian; Radford-Smith, Graeme; Selby, Warwick; Johnston, Michael J; Woods, Rodney; Elliott, P Ross; Bell, Sally J; Brown, Steven J; Connell, William R; Day, Andrew S; Desmond, Paul V; Gearry, Richard B.
Affiliation
  • Wright EK; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia; University of Melbourne, Melbourne, Australia.
  • Kamm MA; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia; University of Melbourne, Melbourne, Australia. Electronic address: mkamm@unimelb.edu.au.
  • De Cruz P; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia; University of Melbourne, Melbourne, Australia.
  • Hamilton AL; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia; University of Melbourne, Melbourne, Australia.
  • Ritchie KJ; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
  • Krejany EO; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
  • Leach S; School of Women's and Children's Health, University of New South Wales, Sydney, Australia.
  • Gorelik A; Melbourne EpiCentre, University of Melbourne, Melbourne, Australia.
  • Liew D; Melbourne EpiCentre, University of Melbourne, Melbourne, Australia.
  • Prideaux L; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia; University of Melbourne, Melbourne, Australia.
  • Lawrance IC; Centre for Inflammatory Bowel Diseases, Fremantle Hospital, Freemantle, Australia; The University of Western Australia, Fremantle, Australia.
  • Andrews JM; Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, Adelaide, Australia; University of Adelaide, Adelaide, Australia.
  • Bampton PA; Department of Gastroenterology and Hepatology, Flinders Medical Centre, Adelaide, Australia; Flinders University, Adelaide, Australia.
  • Jakobovits SL; Department of Gastroenterology, Alfred Health, Melbourne, Australia; Monash University, Melbourne, Australia.
  • Florin TH; Department of Gastroenterology, Mater Health Services, Brisbane, Australia.
  • Gibson PR; Department of Gastroenterology, Alfred Health, Melbourne, Australia; Monash University, Melbourne, Australia.
  • Debinski H; Melbourne Gastrointestinal Investigation Unit, Cabrini Hospital, Melbourne, Australia.
  • Macrae FA; University of Melbourne, Melbourne, Australia; Department of Colorectal Medicine and Genetics, and Department of Medicine, Royal Melbourne Hospital, Melbourne, Australia.
  • Samuel D; Department of Gastroenterology, Bankstown Hospital, Sydney, Australia.
  • Kronborg I; Department of Gastroenterology, Western Hospital, Melbourne, Australia.
  • Radford-Smith G; IBD Group Queensland Institute of Medical Research, University of Queensland, Brisbane, Australia; Department of Gastroenterology, Royal Brisbane and Womens Hospital, Brisbane, Australia.
  • Selby W; AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, Australia.
  • Johnston MJ; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
  • Woods R; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
  • Elliott PR; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
  • Bell SJ; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
  • Brown SJ; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
  • Connell WR; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
  • Day AS; Department of Paediatrics, University of Otago, Christchurch, New Zealand.
  • Desmond PV; Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia; University of Melbourne, Melbourne, Australia.
  • Gearry RB; Department of Medicine, University of Otago, Christchurch, New Zealand.
Gastroenterology ; 148(5): 938-947.e1, 2015 May.
Article in En | MEDLINE | ID: mdl-25620670
ABSTRACT
BACKGROUND &

AIMS:

Crohn's disease (CD) usually recurs after intestinal resection; postoperative endoscopic monitoring and tailored treatment can reduce the chance of recurrence. We investigated whether monitoring levels of fecal calprotectin (FC) can substitute for endoscopic analysis of the mucosa.

METHODS:

We analyzed data collected from 135 participants in a prospective, randomized, controlled trial, performed at 17 hospitals in Australia and 1 hospital in New Zealand, that assessed the ability of endoscopic evaluations and step-up treatment to prevent CD recurrence after surgery. Levels of FC, serum levels of C-reactive protein (CRP), and Crohn's disease activity index (CDAI) scores were measured before surgery and then at 6, 12, and 18 months after resection of all macroscopic Crohn's disease. Ileocolonoscopies were performed at 6 months after surgery in 90 patients and at 18 months after surgery in all patients.

RESULTS:

Levels of FC were measured in 319 samples from 135 patients. The median FC level decreased from 1347 µg/g before surgery to 166 µg/g at 6 months after surgery, but was higher in patients with disease recurrence (based on endoscopic analysis; Rutgeerts score, ≥i2) than in patients in remission (275 vs 72 µg/g, respectively; P < .001). Combined 6- and 18-month levels of FC correlated with the presence (r = 0.42; P < .001) and severity (r = 0.44; P < .001) of CD recurrence, but the CRP level and CDAI score did not. Levels of FC greater than 100 µg/g indicated endoscopic recurrence with 89% sensitivity and 58% specificity, and a negative predictive value (NPV) of 91%; this means that colonoscopy could have been avoided in 47% of patients. Six months after surgery, FC levels less than 51 µg/g in patients in endoscopic remission predicted maintenance of remission (NPV, 79%). In patients with endoscopic recurrence at 6 months who stepped-up treatment, FC levels decreased from 324 µg/g at 6 months to 180 µg/g at 12 months and 109 µg/g at 18 months.

CONCLUSIONS:

In this analysis of data from a prospective clinical trial, FC measurement has sufficient sensitivity and NPV values to monitor for CD recurrence after intestinal resection. Its predictive value might be used to identify patients most likely to relapse. After treatment for recurrence, the FC level can be used to monitor response to treatment. It predicts which patients will have disease recurrence with greater accuracy than CRP level or CDAI score.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Crohn Disease / Leukocyte L1 Antigen Complex / Feces Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: Gastroenterology Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Crohn Disease / Leukocyte L1 Antigen Complex / Feces Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: Gastroenterology Year: 2015 Document type: Article