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How common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? The importance of definition
OBJECTIVES: Many criteria for clinically inactive disease (CID) and minimal disease activity (MDA) have been proposed for juvenile idiopathic arthritis (JIA). It is not known to what degree each of these criteria overlap within a single patient cohort. This study aimed to compare the frequency of MD...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738598/ https://www.ncbi.nlm.nih.gov/pubmed/28389553 http://dx.doi.org/10.1136/annrheumdis-2016-210511 |
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author | Shoop-Worrall, Stephanie J W Verstappen, Suzanne M M Baildam, Eileen Chieng, Alice Davidson, Joyce Foster, Helen Ioannou, Yiannis McErlane, Flora Wedderburn, Lucy R Thomson, Wendy Hyrich, Kimme L |
author_facet | Shoop-Worrall, Stephanie J W Verstappen, Suzanne M M Baildam, Eileen Chieng, Alice Davidson, Joyce Foster, Helen Ioannou, Yiannis McErlane, Flora Wedderburn, Lucy R Thomson, Wendy Hyrich, Kimme L |
author_sort | Shoop-Worrall, Stephanie J W |
collection | PubMed |
description | OBJECTIVES: Many criteria for clinically inactive disease (CID) and minimal disease activity (MDA) have been proposed for juvenile idiopathic arthritis (JIA). It is not known to what degree each of these criteria overlap within a single patient cohort. This study aimed to compare the frequency of MDA and CID across different criteria in a cohort of children with JIA at 1 year following presentation. METHODS: The Childhood Arthritis Prospective Study recruits children at initial presentation to paediatric or adolescent rheumatology in seven UK centres. Children recruited between October 2001 and December 2013 were included. The proportions of children with CID and MDA at 1 year were calculated using four investigator-defined and eight published composite criteria. Missing data were accounted for using multiple imputation under different assumptions. RESULTS: In a cohort of 1415 children and adolescents, 67% patients had no active joints at 1 year. Between 48% and 61% achieved MDA and between 25% and 38% achieved CID using published criteria. Overlap between criteria varied. Of 922 patients in MDA by either the original composite criteria, Juvenile Arthritis Disease Activity Score (JADAS) or clinical JADAS cut-offs, 68% were classified as in MDA by all 3 criteria. Similarly, 44% of 633 children with CID defined by either Wallace's preliminary criteria or the JADAS cut-off were in CID according to both criteria. CONCLUSIONS: In a large JIA prospective inception cohort, a majority of patients have evidence of persistent disease activity after 1 year. Published criteria to capture MDA and CID do not always identify the same groups of patients. This has significant implications when defining and applying treat-to-target strategies. |
format | Online Article Text |
id | pubmed-5738598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57385982018-01-03 How common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? The importance of definition Shoop-Worrall, Stephanie J W Verstappen, Suzanne M M Baildam, Eileen Chieng, Alice Davidson, Joyce Foster, Helen Ioannou, Yiannis McErlane, Flora Wedderburn, Lucy R Thomson, Wendy Hyrich, Kimme L Ann Rheum Dis Clinical and Epidemiological Research OBJECTIVES: Many criteria for clinically inactive disease (CID) and minimal disease activity (MDA) have been proposed for juvenile idiopathic arthritis (JIA). It is not known to what degree each of these criteria overlap within a single patient cohort. This study aimed to compare the frequency of MDA and CID across different criteria in a cohort of children with JIA at 1 year following presentation. METHODS: The Childhood Arthritis Prospective Study recruits children at initial presentation to paediatric or adolescent rheumatology in seven UK centres. Children recruited between October 2001 and December 2013 were included. The proportions of children with CID and MDA at 1 year were calculated using four investigator-defined and eight published composite criteria. Missing data were accounted for using multiple imputation under different assumptions. RESULTS: In a cohort of 1415 children and adolescents, 67% patients had no active joints at 1 year. Between 48% and 61% achieved MDA and between 25% and 38% achieved CID using published criteria. Overlap between criteria varied. Of 922 patients in MDA by either the original composite criteria, Juvenile Arthritis Disease Activity Score (JADAS) or clinical JADAS cut-offs, 68% were classified as in MDA by all 3 criteria. Similarly, 44% of 633 children with CID defined by either Wallace's preliminary criteria or the JADAS cut-off were in CID according to both criteria. CONCLUSIONS: In a large JIA prospective inception cohort, a majority of patients have evidence of persistent disease activity after 1 year. Published criteria to capture MDA and CID do not always identify the same groups of patients. This has significant implications when defining and applying treat-to-target strategies. BMJ Publishing Group 2017-08 2017-04-07 /pmc/articles/PMC5738598/ /pubmed/28389553 http://dx.doi.org/10.1136/annrheumdis-2016-210511 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Clinical and Epidemiological Research Shoop-Worrall, Stephanie J W Verstappen, Suzanne M M Baildam, Eileen Chieng, Alice Davidson, Joyce Foster, Helen Ioannou, Yiannis McErlane, Flora Wedderburn, Lucy R Thomson, Wendy Hyrich, Kimme L How common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? The importance of definition |
title | How common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? The importance of definition |
title_full | How common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? The importance of definition |
title_fullStr | How common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? The importance of definition |
title_full_unstemmed | How common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? The importance of definition |
title_short | How common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? The importance of definition |
title_sort | how common is clinically inactive disease in a prospective cohort of patients with juvenile idiopathic arthritis? the importance of definition |
topic | Clinical and Epidemiological Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738598/ https://www.ncbi.nlm.nih.gov/pubmed/28389553 http://dx.doi.org/10.1136/annrheumdis-2016-210511 |
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