Fecal calprotectin concentration predicts outcome in inflammatory bowel disease after induction therapy with TNFα blocking agents

被引:153
作者
Molander, Pauliina [1 ,2 ]
af Bjorkesten, Clas-Goran
Mustonen, Harri [4 ]
Haapamaki, Johanna
Vauhkonen, Matti [3 ]
Kolho, Kaija-Leena [5 ]
Farkkila, Martti [2 ]
Sipponen, Taina
机构
[1] Maria Helsinki City Hosp, Dept Med, Div Gastroenterol, FIN-00099 Helsinki, Finland
[2] Univ Helsinki, Helsinki, Finland
[3] Univ Helsinki, Cent Hosp, Dept Med, Div Gastroenterol,Jorvi Hosp, Helsinki, Finland
[4] Univ Helsinki, Cent Hosp, Dept Surg, Biomedicum Helsinki, Helsinki, Finland
[5] Univ Helsinki, Cent Hosp, Childrens Hosp, Helsinki, Finland
关键词
Crohn's disease; ulcerative colitis; fecal markers; long-term outcome; infliximab; adalimumab; ILEOCOLONIC CROHNS-DISEASE; MAINTENANCE THERAPY; CLINICAL REMISSION; ULCERATIVE-COLITIS; ENDOSCOPIC SCORE; ACTIVITY INDEX; INFLIXIMAB; LACTOFERRIN; RELAPSE; MULTICENTER;
D O I
10.1002/ibd.22863
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Fecal calprotectin (FC) concentration is a useful surrogate marker for mucosal healing (MH) during tumor necrosis factor alpha (TNFa)-blocking therapy for inflammatory bowel disease (IBD). Our aim was to evaluate whether a normal FC after induction therapy with TNFa antagonist predicts the outcome of IBD patients during maintenance therapy. Methods: Sixty IBD patients (34 Crohn's disease [CD], 26 ulcerative colitis [UC]), treated with TNFa antagonists, either infliximab (n = 42) or adalimumab (n = 18), and having a documented FC level at baseline and after induction therapy were included. Disease activity was evaluated by partial Mayo score without endoscopy or HarveyBradshaw index at baseline, after induction, and at 12 months during maintenance therapy. Results: After induction, FC was normalized (=100 mu g/g) in 31 patients (52%, median 42 mu g/g, range 097), whereas the level remained elevated in 29 patients (48%, median 424 mu g/g, range 1165859). At 12 months, 26/31 (84%, 18 CD, 8 UC) of the patients with normal FC after induction were in clinical remission, whereas only 11/29 (38%, 9 CD, 2 UC) of those with an elevated (=100 mu g/g) postinduction FC were in clinical remission, P < 0.0001. After induction therapy with TNFa antagonists, a cutoff concentration of 139 mu g/g for FC had a sensitivity of 72% and a specificity of 80% to predict a risk of clinically active disease after 1 year. Conclusions: A normal FC after induction therapy with TNFa antagonists predicts sustained clinical remission in the majority of patients on scheduled therapy with active luminal disease. (Inflamm Bowel Dis 2012;)
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页码:2011 / 2017
页数:7
相关论文
共 31 条
[1]   Endoscopic Monitoring of Infliximab Therapy in Crohn's Disease [J].
af Bjorkesten, Clas-Goran ;
Nieminen, Urpo ;
Turunen, Ulla ;
Arkkila, Perttu E. ;
Sipponen, Taina ;
Farkkila, Martti A. .
INFLAMMATORY BOWEL DISEASES, 2011, 17 (04) :947-953
[2]   Review article: is clinical remission the optimum therapeutic goal in the treatment of Crohn's disease [J].
Arnott, IDR ;
Watts, D ;
Ghosh, S .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2002, 16 (05) :857-867
[3]   Mucosal Healing Predicts Sustained Clinical Remission in Patients With Early-Stage Crohn's Disease [J].
Baert, Filip ;
Moortgat, Liesbeth ;
Van Assche, Gert ;
Caenepeel, Philip ;
Vergauwe, Philippe ;
De Vos, Martine ;
Stokkers, Pieter ;
Hommes, Daniel ;
Rutgeerts, Paul ;
Vermeire, Severine ;
D'Haens, Geert .
GASTROENTEROLOGY, 2010, 138 (02) :463-468
[4]   Predicting the Crohn's disease activity index from the Harvey-Bradshaw index [J].
Best, WR .
INFLAMMATORY BOWEL DISEASES, 2006, 12 (04) :304-310
[5]   Review article: monitoring the activity of Crohn's disease [J].
Biancone, L ;
De Nigris, F ;
Blanco, GDV ;
Monteleone, I ;
Vavassori, P ;
Geremia, A ;
Pallone, F .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2002, 16 :29-33
[6]   CORRELATIONS BETWEEN CLINICAL ACTIVITY, ENDOSCOPIC SEVERITY, AND BIOLOGICAL PARAMETERS IN COLONIC OR ILEOCOLONIC CROHNS-DISEASE - A PROSPECTIVE MULTICENTER STUDY OF 121 CASES [J].
CELLIER, C ;
SAHMOUD, T ;
FROGUEL, E ;
ADENIS, A ;
BELAICHE, J ;
BRETAGNE, JF ;
FLORENT, C ;
BOUVRY, M ;
MARY, JY ;
MODIGLIANI, R ;
COLOMBEL, JF ;
CORTOT, A ;
LESCUT, D ;
BITOUN, A ;
LEMANN, M ;
SALMERON, M ;
THEROND, JP ;
VERNISSE, B ;
SEE, A ;
RAOUL, JL .
GUT, 1994, 35 (02) :231-235
[7]   Calprotectin is a stronger predictive marker of relapse in ulcerative colitis than in Crohn's disease [J].
Costa, F ;
Mumolo, MG ;
Ceccarelli, L ;
Bellini, M ;
Romano, MR ;
Sterpi, C ;
Ricchiuti, A ;
Marchi, S ;
Bottai, M .
GUT, 2005, 54 (03) :364-368
[8]   Endoscopic and histological healing with infliximab anti-tumor necrosis factor antibodies in Crohn's disease: A European multicenter trial [J].
D'Haens, G ;
Van Deventer, S ;
Van Hogezand, R ;
Chalmers, D ;
Kothe, C ;
Baert, F ;
Braakman, T ;
Schaible, T ;
Geboes, K ;
Rutgeerts, P .
GASTROENTEROLOGY, 1999, 116 (05) :1029-1034
[9]   A review of activity indices and efficacy end points for clinical trials of medical therapy in adults with ulcerative colitis [J].
D'Haens, Geert ;
Sandborn, William J. ;
Feagan, Brian G. ;
Geboes, Karel ;
Hanauer, Stephen B. ;
Irvine, E. Jan ;
Lemann, Marc ;
Marteau, Philippe ;
Rutgeerts, Paul ;
Scholmerich, Jurgen ;
Sutherland, Lloyd R. .
GASTROENTEROLOGY, 2007, 132 (02) :763-786
[10]   Can calprotectin predict relapse risk in inflammatory bowel disease? [J].
D'Inca, Renata ;
Dal Pont, Elisabetta ;
Di Leo, Vincenza ;
Benazzato, Luca ;
Martinato, Matteo ;
Lamboglia, Francesca ;
Oliva, Lydia ;
Sturniolo, Giacomo Carlo .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2008, 103 (08) :2007-2014