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Predictors of response to methotrexate in juvenile idiopathic arthritis

BACKGROUND: The response to methotrexate so far is unpredictable in patients with juvenile idiopathic arthritis. Thus such predictors have to be determined in a large patient cohort. METHODS: Demographic, clinical, articular and laboratory variables of patients newly treated with methotrexate were a...

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Autores principales: Albarouni, Mohamed, Becker, Ingrid, Horneff, Gerd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138941/
https://www.ncbi.nlm.nih.gov/pubmed/25143761
http://dx.doi.org/10.1186/1546-0096-12-35
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author Albarouni, Mohamed
Becker, Ingrid
Horneff, Gerd
author_facet Albarouni, Mohamed
Becker, Ingrid
Horneff, Gerd
author_sort Albarouni, Mohamed
collection PubMed
description BACKGROUND: The response to methotrexate so far is unpredictable in patients with juvenile idiopathic arthritis. Thus such predictors have to be determined in a large patient cohort. METHODS: Demographic, clinical, articular and laboratory variables of patients newly treated with methotrexate were analysed by bivariate and logistic regression analysis to identify predictors of response to methotrexate. Minimal response was defined by the American College of Rheumatology pediatric (PedACR) 30 and strong response by the PedACR 70 criteria. RESULTS: The patient population consisted of 731 patients. At month 3, 77.4% and at month 12 83.1% of patients were responders according to the PedACR 30 criteria, while 43.1% and 65.9% of patients had a PedACR 70 response at month 3 and at month 12. Thus minimal response was frequently already reached at month 3 while strong response to MTX treatment took usually longer to achieve. In multivariate analysis the number of tender joints (p = 0.002), active joints (p < 0.001), concomitant use of NSAID (p = 0.027) and the parents evaluation of overall well-being (p < 0.001) were significant baseline parameters for minimal response at month 3, while at month 12 the determinants for reaching PedACR 70 were a disease duration < 1 year (p =0.001), a lower number of tender (p <0.001) but a higher number of active joints (p <0.001), a higher score of the parent’s evaluation of child’s pain (p =0.029), and the presence of morning stiffness (p =0.014). CONCLUSIONS: Baseline parameters for minimal response after 3 months of treatment and strong response after 12 months of treatment could be identified. Beside parameters defining activity and severity of disease, the disease duration and the concomitant use of NSAID were influencing factors. Overall the model of prediction could support physicians in making treatment decisions.
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spelling pubmed-41389412014-08-21 Predictors of response to methotrexate in juvenile idiopathic arthritis Albarouni, Mohamed Becker, Ingrid Horneff, Gerd Pediatr Rheumatol Online J Research BACKGROUND: The response to methotrexate so far is unpredictable in patients with juvenile idiopathic arthritis. Thus such predictors have to be determined in a large patient cohort. METHODS: Demographic, clinical, articular and laboratory variables of patients newly treated with methotrexate were analysed by bivariate and logistic regression analysis to identify predictors of response to methotrexate. Minimal response was defined by the American College of Rheumatology pediatric (PedACR) 30 and strong response by the PedACR 70 criteria. RESULTS: The patient population consisted of 731 patients. At month 3, 77.4% and at month 12 83.1% of patients were responders according to the PedACR 30 criteria, while 43.1% and 65.9% of patients had a PedACR 70 response at month 3 and at month 12. Thus minimal response was frequently already reached at month 3 while strong response to MTX treatment took usually longer to achieve. In multivariate analysis the number of tender joints (p = 0.002), active joints (p < 0.001), concomitant use of NSAID (p = 0.027) and the parents evaluation of overall well-being (p < 0.001) were significant baseline parameters for minimal response at month 3, while at month 12 the determinants for reaching PedACR 70 were a disease duration < 1 year (p =0.001), a lower number of tender (p <0.001) but a higher number of active joints (p <0.001), a higher score of the parent’s evaluation of child’s pain (p =0.029), and the presence of morning stiffness (p =0.014). CONCLUSIONS: Baseline parameters for minimal response after 3 months of treatment and strong response after 12 months of treatment could be identified. Beside parameters defining activity and severity of disease, the disease duration and the concomitant use of NSAID were influencing factors. Overall the model of prediction could support physicians in making treatment decisions. BioMed Central 2014-08-13 /pmc/articles/PMC4138941/ /pubmed/25143761 http://dx.doi.org/10.1186/1546-0096-12-35 Text en Copyright © 2014 Albarouni et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Albarouni, Mohamed
Becker, Ingrid
Horneff, Gerd
Predictors of response to methotrexate in juvenile idiopathic arthritis
title Predictors of response to methotrexate in juvenile idiopathic arthritis
title_full Predictors of response to methotrexate in juvenile idiopathic arthritis
title_fullStr Predictors of response to methotrexate in juvenile idiopathic arthritis
title_full_unstemmed Predictors of response to methotrexate in juvenile idiopathic arthritis
title_short Predictors of response to methotrexate in juvenile idiopathic arthritis
title_sort predictors of response to methotrexate in juvenile idiopathic arthritis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138941/
https://www.ncbi.nlm.nih.gov/pubmed/25143761
http://dx.doi.org/10.1186/1546-0096-12-35
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