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Evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis
BACKGROUND: Macrophage activation syndrome (MAS) is a severe and potentially lethal complication of several inflammatory diseases but seems particularly linked to systemic juvenile idiopathic arthritis (sJIA). Standardized diagnostic and treatment guidelines for MAS in sJIA are currently lacking. Th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669611/ https://www.ncbi.nlm.nih.gov/pubmed/26634252 http://dx.doi.org/10.1186/s12969-015-0055-3 |
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author | Boom, V. Anton, J. Lahdenne, P. Quartier, P. Ravelli, A. Wulffraat, N.M. Vastert, S.J. |
author_facet | Boom, V. Anton, J. Lahdenne, P. Quartier, P. Ravelli, A. Wulffraat, N.M. Vastert, S.J. |
author_sort | Boom, V. |
collection | PubMed |
description | BACKGROUND: Macrophage activation syndrome (MAS) is a severe and potentially lethal complication of several inflammatory diseases but seems particularly linked to systemic juvenile idiopathic arthritis (sJIA). Standardized diagnostic and treatment guidelines for MAS in sJIA are currently lacking. The aim of this systematic literature review was to evaluate currently available literature on diagnostic criteria for MAS in sJIA and provide an overview of possible biomarkers for diagnosis, disease activity and treatment response and recent advances in treatment. METHODS: A systematic literature search was performed in MEDLINE, EMBASE and Cochrane. 495 papers were identified. Potentially relevant papers were selected by 3 authors after which full text screening was performed. All selected papers were evaluated by at least two independent experts for validity and level of evidence according to EULAR guidelines. RESULTS: 27 papers were included: 7 on diagnosis, 9 on biomarkers and 11 on treatment. Systematic review of the literature confirmed that there are no validated diagnostic criteria for MAS in sJIA. The preliminary Ravelli criteria, with the addition of ferritin, performed well in a large retrospective case-control study. Recently, an international consortium lead by PRINTO proposed a new set of diagnostic criteria able to distinguish MAS from active sJIA and/or infection with superior performance. Other promising diagnostic biomarkers potentially distinguish MAS complicating sJIA from primary and virus-associated hemophagocytic lymphohistiocytosis. The highest level of evidence for treatment comes from case-series. High dose corticosteroids with or without cyclosporine A were frequently reported as first-line therapy. From the newer treatment modalities, promising responses have been reported with anakinra. CONCLUSION: MAS in sJIA seems to be diagnosed best by the recently proposed PRINTO criteria, although prospective validation is needed. Novel promising biomarkers for sJIA related MAS are in need of prospective validation as well, and are not widely available yet. Currently, treatment of MAS in sJIA relies more on experience than evidence based medicine. Taking into account the severity of MAS and the scarcity of evidence, early expert consultation is recommended as soon as MAS is suspected. |
format | Online Article Text |
id | pubmed-4669611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46696112015-12-05 Evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis Boom, V. Anton, J. Lahdenne, P. Quartier, P. Ravelli, A. Wulffraat, N.M. Vastert, S.J. Pediatr Rheumatol Online J Research Article BACKGROUND: Macrophage activation syndrome (MAS) is a severe and potentially lethal complication of several inflammatory diseases but seems particularly linked to systemic juvenile idiopathic arthritis (sJIA). Standardized diagnostic and treatment guidelines for MAS in sJIA are currently lacking. The aim of this systematic literature review was to evaluate currently available literature on diagnostic criteria for MAS in sJIA and provide an overview of possible biomarkers for diagnosis, disease activity and treatment response and recent advances in treatment. METHODS: A systematic literature search was performed in MEDLINE, EMBASE and Cochrane. 495 papers were identified. Potentially relevant papers were selected by 3 authors after which full text screening was performed. All selected papers were evaluated by at least two independent experts for validity and level of evidence according to EULAR guidelines. RESULTS: 27 papers were included: 7 on diagnosis, 9 on biomarkers and 11 on treatment. Systematic review of the literature confirmed that there are no validated diagnostic criteria for MAS in sJIA. The preliminary Ravelli criteria, with the addition of ferritin, performed well in a large retrospective case-control study. Recently, an international consortium lead by PRINTO proposed a new set of diagnostic criteria able to distinguish MAS from active sJIA and/or infection with superior performance. Other promising diagnostic biomarkers potentially distinguish MAS complicating sJIA from primary and virus-associated hemophagocytic lymphohistiocytosis. The highest level of evidence for treatment comes from case-series. High dose corticosteroids with or without cyclosporine A were frequently reported as first-line therapy. From the newer treatment modalities, promising responses have been reported with anakinra. CONCLUSION: MAS in sJIA seems to be diagnosed best by the recently proposed PRINTO criteria, although prospective validation is needed. Novel promising biomarkers for sJIA related MAS are in need of prospective validation as well, and are not widely available yet. Currently, treatment of MAS in sJIA relies more on experience than evidence based medicine. Taking into account the severity of MAS and the scarcity of evidence, early expert consultation is recommended as soon as MAS is suspected. BioMed Central 2015-12-03 /pmc/articles/PMC4669611/ /pubmed/26634252 http://dx.doi.org/10.1186/s12969-015-0055-3 Text en © Boom et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article Boom, V. Anton, J. Lahdenne, P. Quartier, P. Ravelli, A. Wulffraat, N.M. Vastert, S.J. Evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis |
title | Evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis |
title_full | Evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis |
title_fullStr | Evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis |
title_full_unstemmed | Evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis |
title_short | Evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis |
title_sort | evidence-based diagnosis and treatment of macrophage activation syndrome in systemic juvenile idiopathic arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669611/ https://www.ncbi.nlm.nih.gov/pubmed/26634252 http://dx.doi.org/10.1186/s12969-015-0055-3 |
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