Cargando…
Long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome
INTRODUCTION: Chronic non-bacterial osteomyelitis (CNO) is an autoinflammatory bone-disease of unknown origin. The National Pediatric Rheumatologic Database (NPRD) collects long-term data of children and adolescents with rheumatic diseases including CNO. OBJECTIVE: To assess characteristics, courses...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683360/ https://www.ncbi.nlm.nih.gov/pubmed/38017565 http://dx.doi.org/10.1186/s13075-023-03195-4 |
_version_ | 1785151179195416576 |
---|---|
author | Reiser, Christiane Klotsche, Jens Hospach, Toni Heubner, Georg Windschall, Daniel Trauzeddel, Ralf Groesch, Nadine Niewerth, Martina Minden, Kirsten Girschick, Hermann |
author_facet | Reiser, Christiane Klotsche, Jens Hospach, Toni Heubner, Georg Windschall, Daniel Trauzeddel, Ralf Groesch, Nadine Niewerth, Martina Minden, Kirsten Girschick, Hermann |
author_sort | Reiser, Christiane |
collection | PubMed |
description | INTRODUCTION: Chronic non-bacterial osteomyelitis (CNO) is an autoinflammatory bone-disease of unknown origin. The National Pediatric Rheumatologic Database (NPRD) collects long-term data of children and adolescents with rheumatic diseases including CNO. OBJECTIVE: To assess characteristics, courses, and outcomes of CNO with onset in childhood and adolescence and to identify outcome predictors. METHODS: From 2015 to 2021 patients with a confirmed diagnosis of CNO, who were registered in the NPRD during their first year of disease and at least one follow-up visit, were included in this analysis and observed for up to 4 years. RESULTS: Four hundred patients with recent diagnosis of CNO were enrolled in the NRPD during the study period. After 4 years, patient data documentation was sufficient to be analyzed in 81 patients. A significant decline of clinical and radiological lesions is reported: at inclusion in the registry, the mean number of clinical lesions was 2.0 and 3.0 MRI lesions per patient. A significant decrease of manifestations during 4 years of follow-up (mean clinical lesions 0.5, p < 0.001; mean MRI lesions 0.9 (p < 0.001)) was documented. A significant improvement of physician global disease activity (PGDA), patient-reported overall well-being, and childhood health assessment questionnaire (C-HAQ) was documented. Therapeutically, an increase of disease-modifying anti-rheumatic drugs over the years can be stated, while bisphosphonates rather seem to be considered as a therapeutic DMARD option in the first years of disease. Only 5–7% of the patients had a severe disease course as defined by a PGDA > = 4. Predictors associated with a severe disease course include the site of inflammation (pelvis, lower extremity, clavicle), increased erythrocyte sedimentation rate, and multifocal disease at first documentation. The previously published composite PedCNO disease activity score was analyzed revealing a PedCNO70 in 55% of the patients at 4YFU. CONCLUSION: An improvement of physician global disease activity (PGDA), patient reported overall well-being and imaging-defined disease activity measures was documented, suggesting that inactivity of CNO disease can be reached. PedCNO score and especially PGDA, MRI-defined lesions and in a number of patients also the C-HAQ seem to be reliable parameters for describing disease activity. The identification of risk factors at the beginning of the disease might influence treatment decision in the future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03195-4. |
format | Online Article Text |
id | pubmed-10683360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106833602023-11-30 Long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome Reiser, Christiane Klotsche, Jens Hospach, Toni Heubner, Georg Windschall, Daniel Trauzeddel, Ralf Groesch, Nadine Niewerth, Martina Minden, Kirsten Girschick, Hermann Arthritis Res Ther Research INTRODUCTION: Chronic non-bacterial osteomyelitis (CNO) is an autoinflammatory bone-disease of unknown origin. The National Pediatric Rheumatologic Database (NPRD) collects long-term data of children and adolescents with rheumatic diseases including CNO. OBJECTIVE: To assess characteristics, courses, and outcomes of CNO with onset in childhood and adolescence and to identify outcome predictors. METHODS: From 2015 to 2021 patients with a confirmed diagnosis of CNO, who were registered in the NPRD during their first year of disease and at least one follow-up visit, were included in this analysis and observed for up to 4 years. RESULTS: Four hundred patients with recent diagnosis of CNO were enrolled in the NRPD during the study period. After 4 years, patient data documentation was sufficient to be analyzed in 81 patients. A significant decline of clinical and radiological lesions is reported: at inclusion in the registry, the mean number of clinical lesions was 2.0 and 3.0 MRI lesions per patient. A significant decrease of manifestations during 4 years of follow-up (mean clinical lesions 0.5, p < 0.001; mean MRI lesions 0.9 (p < 0.001)) was documented. A significant improvement of physician global disease activity (PGDA), patient-reported overall well-being, and childhood health assessment questionnaire (C-HAQ) was documented. Therapeutically, an increase of disease-modifying anti-rheumatic drugs over the years can be stated, while bisphosphonates rather seem to be considered as a therapeutic DMARD option in the first years of disease. Only 5–7% of the patients had a severe disease course as defined by a PGDA > = 4. Predictors associated with a severe disease course include the site of inflammation (pelvis, lower extremity, clavicle), increased erythrocyte sedimentation rate, and multifocal disease at first documentation. The previously published composite PedCNO disease activity score was analyzed revealing a PedCNO70 in 55% of the patients at 4YFU. CONCLUSION: An improvement of physician global disease activity (PGDA), patient reported overall well-being and imaging-defined disease activity measures was documented, suggesting that inactivity of CNO disease can be reached. PedCNO score and especially PGDA, MRI-defined lesions and in a number of patients also the C-HAQ seem to be reliable parameters for describing disease activity. The identification of risk factors at the beginning of the disease might influence treatment decision in the future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03195-4. BioMed Central 2023-11-28 2023 /pmc/articles/PMC10683360/ /pubmed/38017565 http://dx.doi.org/10.1186/s13075-023-03195-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Reiser, Christiane Klotsche, Jens Hospach, Toni Heubner, Georg Windschall, Daniel Trauzeddel, Ralf Groesch, Nadine Niewerth, Martina Minden, Kirsten Girschick, Hermann Long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome |
title | Long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome |
title_full | Long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome |
title_fullStr | Long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome |
title_full_unstemmed | Long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome |
title_short | Long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome |
title_sort | long-term follow-up of children with chronic non-bacterial osteomyelitis—assessment of disease activity, risk factors, and outcome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683360/ https://www.ncbi.nlm.nih.gov/pubmed/38017565 http://dx.doi.org/10.1186/s13075-023-03195-4 |
work_keys_str_mv | AT reiserchristiane longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT klotschejens longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT hospachtoni longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT heubnergeorg longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT windschalldaniel longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT trauzeddelralf longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT groeschnadine longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT niewerthmartina longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT mindenkirsten longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome AT girschickhermann longtermfollowupofchildrenwithchronicnonbacterialosteomyelitisassessmentofdiseaseactivityriskfactorsandoutcome |