Cargando…

Differences in MRI findings between subgroups of recent-onset childhood arthritis

BACKGROUND: MRI is sensitive for joint inflammation, but its ability to separate subgroups of arthritis in children has been questioned. Infectious arthritis (IA), postinfectious arthritis (PA), transient arthritis (TA) and juvenile idiopathic arthritis (JIA) are subgroups that may need early, diffe...

Descripción completa

Detalles Bibliográficos
Autores principales: Kirkhus, Eva, Flatø, Berit, Riise, Øystein, Reiseter, Tor, Smith, Hans-Jørgen
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063538/
https://www.ncbi.nlm.nih.gov/pubmed/21136049
http://dx.doi.org/10.1007/s00247-010-1897-y
_version_ 1782200810905534464
author Kirkhus, Eva
Flatø, Berit
Riise, Øystein
Reiseter, Tor
Smith, Hans-Jørgen
author_facet Kirkhus, Eva
Flatø, Berit
Riise, Øystein
Reiseter, Tor
Smith, Hans-Jørgen
author_sort Kirkhus, Eva
collection PubMed
description BACKGROUND: MRI is sensitive for joint inflammation, but its ability to separate subgroups of arthritis in children has been questioned. Infectious arthritis (IA), postinfectious arthritis (PA), transient arthritis (TA) and juvenile idiopathic arthritis (JIA) are subgroups that may need early, different treatment. OBJECTIVE: To determine whether MRI findings differ in IA, PA/TA and JIA in recent-onset childhood arthritis. MATERIALS AND METHODS: Fifty-nine children from a prospective study of incidence of arthritis (n = 216) were, based on clinical and biochemical criteria, examined by MRI. Joint fluid, synovium, bone marrow, soft tissue and cartilage were scored retrospectively and analysed by Pearson chi-square test and logistic regression analysis. RESULTS: Fifty-nine children had MRI of one station. IA was suggested by bone marrow oedema (OR 7.46, P = 0.011) and absence of T1-weighted and T2-weighted low signal intensity synovial tissue (OR 0.06, P = 0.015). Furthermore, soft-tissue oedema and reduced contrast enhancement in the epiphyses were more frequent in children with IA. JIA correlated positively with low signal intensity synovial tissue (OR 13.30, P < 0.001) and negatively with soft-tissue oedema (OR 0.20, P = 0.018). No significant positive determinants were found for PA/TA, but bone marrow oedema, soft-tissue oedema, irregular thickened synovium and low signal intensity synovial tissue was less frequent than in IA/JIA. CONCLUSION: In children with high clinical suspicion of recent onset arthritis, there was a significant difference in the distribution of specific MRI features among the diagnostic groups.
format Text
id pubmed-3063538
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Springer-Verlag
record_format MEDLINE/PubMed
spelling pubmed-30635382011-04-05 Differences in MRI findings between subgroups of recent-onset childhood arthritis Kirkhus, Eva Flatø, Berit Riise, Øystein Reiseter, Tor Smith, Hans-Jørgen Pediatr Radiol Original Article BACKGROUND: MRI is sensitive for joint inflammation, but its ability to separate subgroups of arthritis in children has been questioned. Infectious arthritis (IA), postinfectious arthritis (PA), transient arthritis (TA) and juvenile idiopathic arthritis (JIA) are subgroups that may need early, different treatment. OBJECTIVE: To determine whether MRI findings differ in IA, PA/TA and JIA in recent-onset childhood arthritis. MATERIALS AND METHODS: Fifty-nine children from a prospective study of incidence of arthritis (n = 216) were, based on clinical and biochemical criteria, examined by MRI. Joint fluid, synovium, bone marrow, soft tissue and cartilage were scored retrospectively and analysed by Pearson chi-square test and logistic regression analysis. RESULTS: Fifty-nine children had MRI of one station. IA was suggested by bone marrow oedema (OR 7.46, P = 0.011) and absence of T1-weighted and T2-weighted low signal intensity synovial tissue (OR 0.06, P = 0.015). Furthermore, soft-tissue oedema and reduced contrast enhancement in the epiphyses were more frequent in children with IA. JIA correlated positively with low signal intensity synovial tissue (OR 13.30, P < 0.001) and negatively with soft-tissue oedema (OR 0.20, P = 0.018). No significant positive determinants were found for PA/TA, but bone marrow oedema, soft-tissue oedema, irregular thickened synovium and low signal intensity synovial tissue was less frequent than in IA/JIA. CONCLUSION: In children with high clinical suspicion of recent onset arthritis, there was a significant difference in the distribution of specific MRI features among the diagnostic groups. Springer-Verlag 2010-12-07 2011 /pmc/articles/PMC3063538/ /pubmed/21136049 http://dx.doi.org/10.1007/s00247-010-1897-y Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Kirkhus, Eva
Flatø, Berit
Riise, Øystein
Reiseter, Tor
Smith, Hans-Jørgen
Differences in MRI findings between subgroups of recent-onset childhood arthritis
title Differences in MRI findings between subgroups of recent-onset childhood arthritis
title_full Differences in MRI findings between subgroups of recent-onset childhood arthritis
title_fullStr Differences in MRI findings between subgroups of recent-onset childhood arthritis
title_full_unstemmed Differences in MRI findings between subgroups of recent-onset childhood arthritis
title_short Differences in MRI findings between subgroups of recent-onset childhood arthritis
title_sort differences in mri findings between subgroups of recent-onset childhood arthritis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063538/
https://www.ncbi.nlm.nih.gov/pubmed/21136049
http://dx.doi.org/10.1007/s00247-010-1897-y
work_keys_str_mv AT kirkhuseva differencesinmrifindingsbetweensubgroupsofrecentonsetchildhoodarthritis
AT flatøberit differencesinmrifindingsbetweensubgroupsofrecentonsetchildhoodarthritis
AT riiseøystein differencesinmrifindingsbetweensubgroupsofrecentonsetchildhoodarthritis
AT reisetertor differencesinmrifindingsbetweensubgroupsofrecentonsetchildhoodarthritis
AT smithhansjørgen differencesinmrifindingsbetweensubgroupsofrecentonsetchildhoodarthritis