Literature DB >> 21334460

Levels of C-reactive protein are associated with response to infliximab therapy in patients with Crohn's disease.

Matthias Jürgens1, Jestinah M Mahachie John, Isabelle Cleynen, Fabian Schnitzler, Herma Fidder, Wouter van Moerkercke, Vera Ballet, Maja Noman, Ilse Hoffman, Gert van Assche, Paul J Rutgeerts, Kristel van Steen, Severine Vermeire.   

Abstract

BACKGROUND & AIMS: Infliximab is an antibody against tumor necrosis factor-α that is used to treat patients with moderate to severe Crohn's disease (CD). C-reactive protein (CRP) is a marker used to identify and follow individuals with CD. We analyzed changes in levels of CRP in a large cohort of patients with CD undergoing treatment with infliximab.
METHODS: Serial levels of CRP were analyzed in 718 CD patients. Blood was collected before each infusion; a total of 8845 CRP levels were available for analysis. The correlations between CRP levels and need for dose adjustment, outcomes, and mucosal healing (based on endoscopic analysis of 253 patients) were evaluated. Therapy adjustment was considered successful if therapy continued without need for change. Subgroup analysis was performed by using data from 268 patients who received 8 weeks of maintenance therapy.
RESULTS: More patients with high baseline levels of CRP responded to infliximab than patients with normal levels (90.8% vs 82.6%; P = .014). Early normalization of CRP levels correlated with sustained long-term response (P < .001). CRP levels remained significantly higher among patients who lost their response to infliximab, compared with those with a sustained response (P = .001). At time of loss of response, CRP levels were significantly increased (median, 11.2 mg/L) and did not return to baseline levels (median, 18.2 mg/L; P = .039). CRP correlated with mucosal healing (P = .033).
CONCLUSIONS: CRP is a good marker of disease activity in patients treated with infliximab. Increased levels of CRP indicate mucosal inflammation and a likelihood of clinical relapse.
Copyright © 2011 AGA Institute. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21334460     DOI: 10.1016/j.cgh.2011.02.008

Source DB:  PubMed          Journal:  Clin Gastroenterol Hepatol        ISSN: 1542-3565            Impact factor:   11.382


  54 in total

1.  IBD: CRP is a good long-term biomarker.

Authors:  Isobel Franks
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2011-07-04       Impact factor: 46.802

Review 2.  Biomarkers in inflammatory bowel disease: current practices and recent advances.

Authors:  Heba N Iskandar; Matthew A Ciorba
Journal:  Transl Res       Date:  2012-02-01       Impact factor: 7.012

Review 3.  The use of prognostic factors in inflammatory bowel diseases.

Authors:  Thomas Billiet; Marc Ferrante; Gert Van Assche
Journal:  Curr Gastroenterol Rep       Date:  2014-11

4.  Long-Term Outcomes of Adalimumab Treatment in 254 Patients with Crohn's Disease: A Hospital-Based Cohort Study from Korea.

Authors:  Hyungil Seo; Byong Duk Ye; Eun Mi Song; Sun-Ho Lee; Kiju Chang; Ho-Su Lee; Sung Wook Hwang; Sang Hyoung Park; Dong-Hoon Yang; Kyung-Jo Kim; Jeong-Sik Byeon; Seung-Jae Myung; Suk-Kyun Yang
Journal:  Dig Dis Sci       Date:  2017-08-18       Impact factor: 3.199

5.  A SPECIAL MEETING REVIEW EDITION: Highlights in Anti-Tumor Necrosis Factor Monitoring and Antibody Monitoring From the 2014 DDW Meeting: Digestive Disease Week 2014 May 3-6, 2014 • Chicago, Illinois: Special Reporting on:• Therapeutic Monitoring of Anti-TNF Levels and Antibodies to Predict Response and Achieve Mucosal Healing• Prospective Therapeutic Drug Monitoring and Optimization of Infliximab Maintenance Therapy in IBD• Classification of Non-IBD, Crohn's Disease and Ulcerative Colitis in a Young Patient Population Using a Multi-Marker Diagnostic Panel• Persistence of Antibodies to Infliximab for More Than Two Months Predicts Loss of Response to Infliximab in Inflammatory Bowel Diseases• Pre-Operative Serological Markers May Predict Postoperative Crohn's Disease Recurrence: Results From a Prospective Mono-Centric Trial• Antibodies and Levels of Biologies-Reactive vs Proactive Measurements• Higher 6-Thioguanine Nucleotide Concentrations Are Associated With Higher Trough Levels of Infliximab in Patients on Combination Therapy• The Clinical and Immunological Significance of Low Levels of Infliximab in the Absence of Anti-lnfliximab Antibodies in Patients With IBD• Antibodies to Adalimumab Predict Inflammation in Crohn's Patients on Maintenance Adalimumab Therapy• ATG16L1 Genotype Is Associated With Response to Anti-TNFWith Expert Commentary by:William J. Sandborn, MDProfessor and Chief, Division of Gastroenterology Director, UCSD IBD CenterUC San Diego Health SystemLa Jolla, California.

Authors: 
Journal:  Gastroenterol Hepatol (N Y)       Date:  2014-07

Review 6.  Mucosal healing in inflammatory bowel disease: Expanding horizon.

Authors:  Jimil Shah; Manik Lal Thakur; Usha Dutta
Journal:  Indian J Gastroenterol       Date:  2019-04-29

7.  Outcomes following infliximab therapy for pediatric patients hospitalized with refractory colitis-predominant IBD.

Authors:  Tolulope O Falaiye; Keisha R Mitchell; Zengqi Lu; Benjamin R Saville; Sara N Horst; Dedrick E Moulton; David A Schwartz; Keith T Wilson; Michael J Rosen
Journal:  J Pediatr Gastroenterol Nutr       Date:  2014-02       Impact factor: 2.839

Review 8.  Utility of surrogate markers for the prediction of relapses in inflammatory bowel diseases.

Authors:  Jason Orlando Dimitri Musci; Jack Stephen Cornish; Jan Däbritz
Journal:  J Gastroenterol       Date:  2016-03-14       Impact factor: 7.527

Review 9.  Predicting durable response or resistance to antitumor necrosis factor therapy in inflammatory bowel disease.

Authors:  Uri Kopylov; Ernest Seidman
Journal:  Therap Adv Gastroenterol       Date:  2016-04-01       Impact factor: 4.409

10.  C-reactive protein is an indicator of serum infliximab level in predicting loss of response in patients with Crohn's disease.

Authors:  Toshifumi Hibi; Atsushi Sakuraba; Mamoru Watanabe; Satoshi Motoya; Hiroaki Ito; Noriko Sato; Toru Yoshinari; Kenta Motegi; Yoshitaka Kinouchi; Masakazu Takazoe; Yasuo Suzuki; Takayuki Matsumoto; Kazuhiko Kawakami; Takayuki Matsumoto; Ichiro Hirata; Shinji Tanaka; Toshifumi Ashida; Toshiyuki Matsui
Journal:  J Gastroenterol       Date:  2013-04-20       Impact factor: 7.527

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