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HLA-B*27 is associated with CNO in a European cohort
OBJECTIVES: To determine the influence of HLA-B27 positivity on risk of developing chronic nonbacterial osteomyelitis (CNO). METHODS: HLA-B*27 genotype was assessed in 3 European CNO populations and compared with local control populations (572 cases, 33,256 controls). Regional or whole-body MRI was...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240753/ https://www.ncbi.nlm.nih.gov/pubmed/37277844 http://dx.doi.org/10.1186/s12969-023-00826-7 |
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author | O’Leary, Daire Al Julandani, Dalila Ali Zia, Muhammad Klotsche, Jens Minden, Kirsten Roderick, Marion Ramanan, Athimalaipet V. Killeen, Orla G. Wilson, Anthony G. |
author_facet | O’Leary, Daire Al Julandani, Dalila Ali Zia, Muhammad Klotsche, Jens Minden, Kirsten Roderick, Marion Ramanan, Athimalaipet V. Killeen, Orla G. Wilson, Anthony G. |
author_sort | O’Leary, Daire |
collection | PubMed |
description | OBJECTIVES: To determine the influence of HLA-B27 positivity on risk of developing chronic nonbacterial osteomyelitis (CNO). METHODS: HLA-B*27 genotype was assessed in 3 European CNO populations and compared with local control populations (572 cases, 33,256 controls). Regional or whole-body MRI was performed at diagnosis and follow-up in all cases which reduces the risk of disease misclassification. Genotyping was performed using either next generation DNA sequencing or PCR based molecular typing. Statistical analysis used Fisher’s exact test with Bonferroni correction and a fixed effects model for meta-analysis of odds ratios. RESULTS: HLA-B*27 frequency was higher in all 3 populations compared with local controls (combined odds ratio (OR) = 2.2, p-value = 3 × 10(–11)). This association was much stronger in male compared with female cases (OR = 1.99, corrected p-value = 0.015). However, the HLA-B*27 status was not statistically significantly associated with co-occurrence of psoriasis, arthritis or inflammatory bowel disease. CONCLUSION: Carriage of HLA-B*27 is associated with greater risk of developing CNO, particularly in male cases. |
format | Online Article Text |
id | pubmed-10240753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102407532023-06-06 HLA-B*27 is associated with CNO in a European cohort O’Leary, Daire Al Julandani, Dalila Ali Zia, Muhammad Klotsche, Jens Minden, Kirsten Roderick, Marion Ramanan, Athimalaipet V. Killeen, Orla G. Wilson, Anthony G. Pediatr Rheumatol Online J Research Article OBJECTIVES: To determine the influence of HLA-B27 positivity on risk of developing chronic nonbacterial osteomyelitis (CNO). METHODS: HLA-B*27 genotype was assessed in 3 European CNO populations and compared with local control populations (572 cases, 33,256 controls). Regional or whole-body MRI was performed at diagnosis and follow-up in all cases which reduces the risk of disease misclassification. Genotyping was performed using either next generation DNA sequencing or PCR based molecular typing. Statistical analysis used Fisher’s exact test with Bonferroni correction and a fixed effects model for meta-analysis of odds ratios. RESULTS: HLA-B*27 frequency was higher in all 3 populations compared with local controls (combined odds ratio (OR) = 2.2, p-value = 3 × 10(–11)). This association was much stronger in male compared with female cases (OR = 1.99, corrected p-value = 0.015). However, the HLA-B*27 status was not statistically significantly associated with co-occurrence of psoriasis, arthritis or inflammatory bowel disease. CONCLUSION: Carriage of HLA-B*27 is associated with greater risk of developing CNO, particularly in male cases. BioMed Central 2023-06-05 /pmc/articles/PMC10240753/ /pubmed/37277844 http://dx.doi.org/10.1186/s12969-023-00826-7 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 Article O’Leary, Daire Al Julandani, Dalila Ali Zia, Muhammad Klotsche, Jens Minden, Kirsten Roderick, Marion Ramanan, Athimalaipet V. Killeen, Orla G. Wilson, Anthony G. HLA-B*27 is associated with CNO in a European cohort |
title | HLA-B*27 is associated with CNO in a European cohort |
title_full | HLA-B*27 is associated with CNO in a European cohort |
title_fullStr | HLA-B*27 is associated with CNO in a European cohort |
title_full_unstemmed | HLA-B*27 is associated with CNO in a European cohort |
title_short | HLA-B*27 is associated with CNO in a European cohort |
title_sort | hla-b*27 is associated with cno in a european cohort |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240753/ https://www.ncbi.nlm.nih.gov/pubmed/37277844 http://dx.doi.org/10.1186/s12969-023-00826-7 |
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