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Sacroiliac joint involvement in children with inflammatory bowel diseases

OBJECTIVE: Sacroiliitis (SI), an inflammatory arthropathy, may accompany pediatric inflammatory bowel diseases (IBDs), present with non- specific back pain, hence might be unnoticed. The aims of this study were to assess the frequency of the SI in children with IBD and determine the characteristics...

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Autores principales: Gerenli, Nelgin, Sozeri, Betul, Kalin, Sevinc, Kirmizibekmez, Heves, Celtik, Coskun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Health Directorate of Istanbul 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889211/
https://www.ncbi.nlm.nih.gov/pubmed/35340318
http://dx.doi.org/10.14744/nci.2021.24572
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author Gerenli, Nelgin
Sozeri, Betul
Kalin, Sevinc
Kirmizibekmez, Heves
Celtik, Coskun
author_facet Gerenli, Nelgin
Sozeri, Betul
Kalin, Sevinc
Kirmizibekmez, Heves
Celtik, Coskun
author_sort Gerenli, Nelgin
collection PubMed
description OBJECTIVE: Sacroiliitis (SI), an inflammatory arthropathy, may accompany pediatric inflammatory bowel diseases (IBDs), present with non- specific back pain, hence might be unnoticed. The aims of this study were to assess the frequency of the SI in children with IBD and determine the characteristics of the association of SI with the clinical hallmarks of the IBD. METHODS: In this prospective, cross sectional study, twenty-seven children with IBD, 7–18 years of age were evaluated. Patients with low back pain or stiffness, alternating buttock pain, or hip pain were examined for the presence of SI. The radiologic manifestations on X-ray suggesting sacroilitis were confirmed with Magnetic resonance imaging (MRI). RESULTS: Twenty-seven children (16 girls, female/male=1.45), with mean age of 12.55±3.6 years, of which 52% had ulcerative colitis (UC), 41% had Crohn’s disease (CD), and two had indeterminate colitis (IC). The median time from IBD diagnosis was 6.0 (18.0) months for patients with SI and 12.0 (13.5) months for patients without SI. Low back pain or stiffness was observed in 13 patients (48%). SI was present in eight (30%) of the children with IBD. The patients with CD were more prone to SI (45% of CD vs. 21% of UC patients). All patients with SI were negative for HLA-B27 genotyping. The disease activity and gender were not associated with increased risk for SI. MRI was remarkable for bone marrow edema in all of the patient, followed by erosions in six of them (75%), synovial enhancement observed in five (63%), and erosion associated enthesitis of the pelvic region was observed in two (25%) of the patients. CONCLUSION: SI may remain obscured in children with IBD. Children with CD are more prone to SI than those with UC. Pediatric rheumatology-pediatric gastroenterology collaboration might augment screening in at-risk patients.
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spelling pubmed-88892112022-03-24 Sacroiliac joint involvement in children with inflammatory bowel diseases Gerenli, Nelgin Sozeri, Betul Kalin, Sevinc Kirmizibekmez, Heves Celtik, Coskun North Clin Istanb Original Article - Pediatrics OBJECTIVE: Sacroiliitis (SI), an inflammatory arthropathy, may accompany pediatric inflammatory bowel diseases (IBDs), present with non- specific back pain, hence might be unnoticed. The aims of this study were to assess the frequency of the SI in children with IBD and determine the characteristics of the association of SI with the clinical hallmarks of the IBD. METHODS: In this prospective, cross sectional study, twenty-seven children with IBD, 7–18 years of age were evaluated. Patients with low back pain or stiffness, alternating buttock pain, or hip pain were examined for the presence of SI. The radiologic manifestations on X-ray suggesting sacroilitis were confirmed with Magnetic resonance imaging (MRI). RESULTS: Twenty-seven children (16 girls, female/male=1.45), with mean age of 12.55±3.6 years, of which 52% had ulcerative colitis (UC), 41% had Crohn’s disease (CD), and two had indeterminate colitis (IC). The median time from IBD diagnosis was 6.0 (18.0) months for patients with SI and 12.0 (13.5) months for patients without SI. Low back pain or stiffness was observed in 13 patients (48%). SI was present in eight (30%) of the children with IBD. The patients with CD were more prone to SI (45% of CD vs. 21% of UC patients). All patients with SI were negative for HLA-B27 genotyping. The disease activity and gender were not associated with increased risk for SI. MRI was remarkable for bone marrow edema in all of the patient, followed by erosions in six of them (75%), synovial enhancement observed in five (63%), and erosion associated enthesitis of the pelvic region was observed in two (25%) of the patients. CONCLUSION: SI may remain obscured in children with IBD. Children with CD are more prone to SI than those with UC. Pediatric rheumatology-pediatric gastroenterology collaboration might augment screening in at-risk patients. Health Directorate of Istanbul 2021-02-08 /pmc/articles/PMC8889211/ /pubmed/35340318 http://dx.doi.org/10.14744/nci.2021.24572 Text en Copyright © by by Istanbul Provincial Directorate of Health - Available online at www.northclinist.com https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
spellingShingle Original Article - Pediatrics
Gerenli, Nelgin
Sozeri, Betul
Kalin, Sevinc
Kirmizibekmez, Heves
Celtik, Coskun
Sacroiliac joint involvement in children with inflammatory bowel diseases
title Sacroiliac joint involvement in children with inflammatory bowel diseases
title_full Sacroiliac joint involvement in children with inflammatory bowel diseases
title_fullStr Sacroiliac joint involvement in children with inflammatory bowel diseases
title_full_unstemmed Sacroiliac joint involvement in children with inflammatory bowel diseases
title_short Sacroiliac joint involvement in children with inflammatory bowel diseases
title_sort sacroiliac joint involvement in children with inflammatory bowel diseases
topic Original Article - Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889211/
https://www.ncbi.nlm.nih.gov/pubmed/35340318
http://dx.doi.org/10.14744/nci.2021.24572
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