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How many biomarker measurements are needed to predict prognosis in Crohn's disease patients under infliximab?-A prospective study.
Magro, Fernando; Estevinho, Maria Manuela; Catalano, Gaia; Patita, Marta; Arroja, Bruno; Lago, Paula; Rosa, Isadora; Tavares de Sousa, Helena; Ministro, Paula; Mocanu, Irina; Vieira, Ana; Castela, Joana; Moleiro, Joana; Roseira, Joana; Cancela, Eugénia; Sousa, Paula; Portela, Francisco; Correia, Luís; Moreira, Paula; Santiago, Mafalda; Dias, Sandra; Afonso, Joana; Danese, Silvio; Peyrin-Biroulet, Laurent; Dias, Cláudia Camila.
Afiliación
  • Magro F; Department of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.
  • Estevinho MM; Department of Gastroenterology, São João Hospital University Centre, Porto, Portugal.
  • Catalano G; Center for Health Technology and Services Research (CINTESIS), Porto, Portugal.
  • Patita M; Unidade de Farmacologia Clínica, São João Hospital University Centre, Porto, Portugal.
  • Arroja B; Department of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.
  • Lago P; Department of Gastroenterology, Vila Nova de Gaia Espinho Hospital Center, Vila Nova de Gaia, Portugal.
  • Rosa I; Department of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.
  • Tavares de Sousa H; Department of Gastroenterology, Garcia da Orta Hospital, Almada, Portugal.
  • Ministro P; Department of Gastroenterology, Braga Hospital, Braga, Portugal.
  • Mocanu I; Department of Gastroenterology, Porto Hospital University Centre, Porto, Portugal.
  • Vieira A; Department of Gastroenterology, IPOLFG, EPE, Lisbon, Portugal.
  • Castela J; Department of Gastroenterology, Algarve Hospital University Centre - Portimão Unit, Portimão, Portugal.
  • Moleiro J; ABC - Algarve Biomedical Center, University of Algarve, Faro, Portugal.
  • Roseira J; Department of Gastroenterology, Viseu-Tondela Hospital Centre, Viseu, Portugal.
  • Cancela E; Department of Gastroenterology, Garcia da Orta Hospital, Almada, Portugal.
  • Sousa P; Department of Gastroenterology, Garcia da Orta Hospital, Almada, Portugal.
  • Portela F; Department of Gastroenterology, IPOLFG, EPE, Lisbon, Portugal.
  • Correia L; Department of Gastroenterology, IPOLFG, EPE, Lisbon, Portugal.
  • Moreira P; Department of Gastroenterology, Algarve Hospital University Centre - Portimão Unit, Portimão, Portugal.
  • Santiago M; Department of Gastroenterology, Viseu-Tondela Hospital Centre, Viseu, Portugal.
  • Dias S; Department of Gastroenterology, Viseu-Tondela Hospital Centre, Viseu, Portugal.
  • Afonso J; Department of Gastroenterology, Coimbra Hospital University Centre, Coimbra, Portugal.
  • Danese S; Department of Gastroenterology, Northern Lisbon University Hospital Centre, Lisbon, Portugal.
  • Peyrin-Biroulet L; Unidade de Farmacologia Clínica, São João Hospital University Centre, Porto, Portugal.
  • Dias CC; Center for Health Technology and Services Research (CINTESIS), Porto, Portugal.
United European Gastroenterol J ; 11(6): 531-541, 2023 07.
Article en En | MEDLINE | ID: mdl-37318072
BACKGROUND: Timely stratification of Crohn's disease (CD) is essential for patients' management. The use of noninvasive accurate biomarkers is key to monitor treatment and to pursue mucosal healing, the ultimate treatment endpoint in CD. OBJECTIVE: We aimed to evaluate the performance of readily available biomarkers and develop risk matrices to predict CD progression. METHODS: Data from 289 CD patients receiving infliximab (IFX) maintenance therapy for 2 years was collected; those patients were included in DIRECT, a prospective multicenter observational study. Disease progression was evaluated using two composite outcomes incorporating clinical and drug-related factors, the first including IFX dose and/or frequency adjustments. Univariate and multivariable logistic regressions were used to calculate the odds ratios (OR) and to develop risk matrices. RESULTS: The isolated presence of anemia at least once during follow-up was a significant predictor of disease progression (OR 2.436 and 3.396 [p ≤ 0.001] for composite outcomes 1 and 2, respectively) regardless of confounding factors. Isolated highly elevated C-reactive protein (CRP; >10.0 mg/L) and fecal calprotectin (FC; >500.0 µg/g) in at least one visit were also significant predictors, while milder elevations (3.1-10.0 mg/L and 250.1-500.0 µg/g) were only relevant when detected in at least two visits (consecutive or not). The combination of biomarkers in risk matrices had good ability to predict progression; patients simultaneously presenting anemia, highly elevated CRP and FC at least once had 42%-63% probability of achieving the composite outcomes. CONCLUSION: The combined evaluation of hemoglobin, CRP, and FC in at least one time point and their incorporation into risk matrices seems to be the optimal strategy for CD management, as data from additional visits did not meaningfully influence the predictions and may delay decision-making.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Crohn Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Límite: Humans Idioma: En Revista: United European Gastroenterol J Año: 2023 Tipo del documento: Article País de afiliación: Portugal Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Crohn Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Límite: Humans Idioma: En Revista: United European Gastroenterol J Año: 2023 Tipo del documento: Article País de afiliación: Portugal Pais de publicación: Reino Unido