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Comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial
INTRODUCTION: Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disorder in children. Although methotrexate (MTX) is the first line disease-modifying antirheumatic drug for JIA, many patients do not respond well or cannot tolerate MTX. The aim of this study was to compare the...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044028/ https://www.ncbi.nlm.nih.gov/pubmed/36998586 http://dx.doi.org/10.5114/reum/161317 |
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author | Rezaieyazdi, Zahra Ravanshad, Sahar Khodashahi, Mandana Bokaeian, Maliheh Mehrad Majd, Hassan Salari, Masoumeh |
author_facet | Rezaieyazdi, Zahra Ravanshad, Sahar Khodashahi, Mandana Bokaeian, Maliheh Mehrad Majd, Hassan Salari, Masoumeh |
author_sort | Rezaieyazdi, Zahra |
collection | PubMed |
description | INTRODUCTION: Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disorder in children. Although methotrexate (MTX) is the first line disease-modifying antirheumatic drug for JIA, many patients do not respond well or cannot tolerate MTX. The aim of this study was to compare the effect of combination therapy of MTX and leflunomide (LFN) with MTX in patients who do not respond to MTX. MATERIAL AND METHODS: Eighteen patients (2–20 years old) with polyarticular, oligoarticular or extended oligoarticular subtypes of JIA who did not respond to conventional JIA therapy participated in this double-blind, placebo-controlled, randomized trial. The intervention group received LFN and MTX for 3 months while the control group received oral placebo and MTX at a similar dose to the intervention group. Response to treatment was assessed every 4 weeks using the American College of Rheumatology Pediatric criteria (ACRPed) scale. RESULTS: Clinical criteria, including number of active joints and restricted joints, physician and patient global assessment, Childhood Health Assessment Questionnaire (CHAQ38) score, and serum erythrocyte sedimentation ratelevel, did not differ significantly between groups at baseline and at the end of the 4(th) and 8(th) weeks of treatment. Only the CHAQ38 score was significantly higher in the intervention group at the end of the 12(th) week of treatment. Analysis of the effect of treatment on study parameters revealed that only the global patient assessment score differed significantly between groups (p = 0.003). CONCLUSIONS: The results of this study showed that combining LFN with MTX does not improve clinical outcomes of JIA and may increase side effects in patients who do not respond to MTX. |
format | Online Article Text |
id | pubmed-10044028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie |
record_format | MEDLINE/PubMed |
spelling | pubmed-100440282023-03-29 Comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial Rezaieyazdi, Zahra Ravanshad, Sahar Khodashahi, Mandana Bokaeian, Maliheh Mehrad Majd, Hassan Salari, Masoumeh Reumatologia Original Paper INTRODUCTION: Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disorder in children. Although methotrexate (MTX) is the first line disease-modifying antirheumatic drug for JIA, many patients do not respond well or cannot tolerate MTX. The aim of this study was to compare the effect of combination therapy of MTX and leflunomide (LFN) with MTX in patients who do not respond to MTX. MATERIAL AND METHODS: Eighteen patients (2–20 years old) with polyarticular, oligoarticular or extended oligoarticular subtypes of JIA who did not respond to conventional JIA therapy participated in this double-blind, placebo-controlled, randomized trial. The intervention group received LFN and MTX for 3 months while the control group received oral placebo and MTX at a similar dose to the intervention group. Response to treatment was assessed every 4 weeks using the American College of Rheumatology Pediatric criteria (ACRPed) scale. RESULTS: Clinical criteria, including number of active joints and restricted joints, physician and patient global assessment, Childhood Health Assessment Questionnaire (CHAQ38) score, and serum erythrocyte sedimentation ratelevel, did not differ significantly between groups at baseline and at the end of the 4(th) and 8(th) weeks of treatment. Only the CHAQ38 score was significantly higher in the intervention group at the end of the 12(th) week of treatment. Analysis of the effect of treatment on study parameters revealed that only the global patient assessment score differed significantly between groups (p = 0.003). CONCLUSIONS: The results of this study showed that combining LFN with MTX does not improve clinical outcomes of JIA and may increase side effects in patients who do not respond to MTX. Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 2023-03-08 2023 /pmc/articles/PMC10044028/ /pubmed/36998586 http://dx.doi.org/10.5114/reum/161317 Text en Copyright: © 2023 Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Original Paper Rezaieyazdi, Zahra Ravanshad, Sahar Khodashahi, Mandana Bokaeian, Maliheh Mehrad Majd, Hassan Salari, Masoumeh Comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial |
title | Comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial |
title_full | Comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial |
title_fullStr | Comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial |
title_full_unstemmed | Comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial |
title_short | Comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial |
title_sort | comparison of the efficacy and safety of methotrexate alone or in combination with leflunomide in the treatment of juvenile idiopathic arthritis: a double-blind, placebo-controlled, randomized trial |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044028/ https://www.ncbi.nlm.nih.gov/pubmed/36998586 http://dx.doi.org/10.5114/reum/161317 |
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