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Does fecal calprotectin predict short-term relapse after stopping TNFα-blocking agents in inflammatory bowel disease patients in deep remission?
Molander, Pauliina; Färkkilä, Martti; Ristimäki, Ari; Salminen, Kimmo; Kemppainen, Helena; Blomster, Timo; Koskela, Ritva; Jussila, Airi; Rautiainen, Henna; Nissinen, Markku; Haapamäki, Johanna; Arkkila, Perttu; Nieminen, Urpo; Kuisma, Juha; Punkkinen, Jari; Kolho, Kaija-Leena; Mustonen, Harri; Sipponen, Taina.
Afiliación
  • Molander P; Maria Helsinki City Hospital and University of Helsinki, Helsinki, Finland pauliina.molander@welho.com.
  • Färkkilä M; Department of Medicine, Division of Gastroenterology, Helsinki University Central Hospital, Helsinki, Finland University of Helsinki, Institute of Clinical Medicine, Department of Medicine, Division of Gastroenterology, Helsinki, Finland.
  • Ristimäki A; Department of Pathology, HUSLAB and Haartman Institute, Helsinki University Central Hospital and Genome-Scale Biology, Research Programs Unit, University of Helsinki, Helsinki, Finland.
  • Salminen K; Department of Medicine, Division of Gastroenterology, Turku University Central Hospital, Turku, Finland.
  • Kemppainen H; Department of Medicine, Division of Gastroenterology, Turku University Central Hospital, Turku, Finland.
  • Blomster T; Department of Medicine, Division of Gastroenterology, Oulu University Central Hospital, Oulu, Finland.
  • Koskela R; Department of Medicine, Division of Gastroenterology, Oulu University Central Hospital, Oulu, Finland.
  • Jussila A; Department of Gastroenterology and Alimentary Tract Surgery, Tampere University Hospital, Tampere, Finland.
  • Rautiainen H; Department of Medicine, Division of Gastroenterology, Helsinki University Central Hospital, Jorvi Hospital, Espoo, Finland.
  • Nissinen M; Department of Medicine, Division of Gastroenterology, Helsinki University Central Hospital, Peijas Hospital, Vantaa, Finland.
  • Haapamäki J; Department of Medicine, Division of Gastroenterology, Helsinki University Central Hospital, Helsinki, Finland.
  • Arkkila P; Department of Medicine, Division of Gastroenterology, Helsinki University Central Hospital, Helsinki, Finland.
  • Nieminen U; Department of Medicine, Division of Gastroenterology, Helsinki University Central Hospital, Helsinki, Finland.
  • Kuisma J; Department of Medicine, Hyvinkää Hospital, Hyvinkää, Finland.
  • Punkkinen J; Department of Medicine, Porvoo Hospital, Porvoo, Finland.
  • Kolho KL; Children's Hospital, Helsinki University Central Hospital, Helsinki, Finland University of Helsinki, Institute of Clinical Medicine, Department of Medicine, Division of Gastroenterology, Helsinki, Finland.
  • Mustonen H; Helsinki University Central Hospital, Department of Surgery, Biomedicum Helsinki, Finland.
  • Sipponen T; Department of Medicine, Division of Gastroenterology, Helsinki University Central Hospital, Helsinki, Finland.
J Crohns Colitis ; 9(1): 33-40, 2015 Jan.
Article en En | MEDLINE | ID: mdl-25052347
BACKGROUND AND AIMS: This prospective multicenter study examined whether elevated fecal calprotec tin (FC) concentrations after stopping TNFα-blocking therapy can predict clinical or endoscopic relapse. In addition, we evaluated the impact of histological remission on the relapse risk. METHODS: We enrolled inflammatory bowel disease (IBD) patients who were in clinical, endoscopic, and FC-based (< 100 µg/g) remission after a minimum 11 months of TNFα-blocking therapy. The patients were followed-up for 12 months after the discontinuation of TNFα-blocking therapy. FC was collected monthly for the first 6 months and thereafter every second month. Ileocolonoscopy was performed at inclusion, at 4 months, at the study end, and at the time of clinical relapse. RESULTS: Of 52 enrolled patients, 49 (16 Crohn's disease, 33 ulcerative colitis/IBD unclassified) provided the stool samples requested and comprised the study group. During the follow-up, 15/49 (31%) relapsed, whereas 34 (69%) remained in remission. Patients relapsing showed constantly elevated FC levels for a median of 94 (13-317) days before the relapse. Significant increase in median FC levels was seen 2 (p = 0.0014), 4 (p = 0.0056), and 6 (p = 0.0029) months before endoscopic relapse. Constantly normal FC concentrations during the follow-up were highly predictive for clinical and endoscopic remission. Normal FC concentrations in patients with remission were associated with histological remission. CONCLUSION: FC seems to increase and remain elevated before clinical or endoscopic relapse, suggesting that it can be used as a surrogate marker for predicting and identifying patients requiring close follow-up in clinical practice.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fármacos Gastrointestinales / Enfermedades Inflamatorias del Intestino / Factor de Necrosis Tumoral alfa / Complejo de Antígeno L1 de Leucocito / Heces Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Crohns Colitis Asunto de la revista: GASTROENTEROLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Finlandia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fármacos Gastrointestinales / Enfermedades Inflamatorias del Intestino / Factor de Necrosis Tumoral alfa / Complejo de Antígeno L1 de Leucocito / Heces Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Crohns Colitis Asunto de la revista: GASTROENTEROLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Finlandia
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