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Association of HLA-B27 status and gender with sacroiliitis in patients with ankylosing spondylitis

Objective: To observe the influence of human leucocyte antigen B27 (HLA-B27) status and gender on sacroiliitis on computed tomography (CT) in ankylosingspondylitis (AS). Methods: We reviewed the archived medical records of the AS inpatients admitted in the Rheumatology Department of the First Affili...

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Autores principales: Xiong, Jiangbiao, Chen, Jing, Tu, Jianxin, Ye, Wenjing, Zhang, Zhiyong, Liu, Qiaoqiong, Zhu, Xiaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publicaitons 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955535/
https://www.ncbi.nlm.nih.gov/pubmed/24639824
http://dx.doi.org/10.12669/pjms.301.3896
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author Xiong, Jiangbiao
Chen, Jing
Tu, Jianxin
Ye, Wenjing
Zhang, Zhiyong
Liu, Qiaoqiong
Zhu, Xiaochun
author_facet Xiong, Jiangbiao
Chen, Jing
Tu, Jianxin
Ye, Wenjing
Zhang, Zhiyong
Liu, Qiaoqiong
Zhu, Xiaochun
author_sort Xiong, Jiangbiao
collection PubMed
description Objective: To observe the influence of human leucocyte antigen B27 (HLA-B27) status and gender on sacroiliitis on computed tomography (CT) in ankylosingspondylitis (AS). Methods: We reviewed the archived medical records of the AS inpatients admitted in the Rheumatology Department of the First Affiliated Hospital of Wenzhou Medical University during the period from January 2007 through January 2013 and finally 386 patients were included in the study. The severity of sacroiliitis on CT was evaluated according to the grading used in the modified New York criteria for AS. Two-way classification analysis of variance (ANOVA) was employed to examine the effect of HLA-B27 status and gender on age at disease onset. The impact of HLA-B27 and gender on sacroiliitis on CT was tested by univariate and multivariate logistic regression analyses. Results: There were 350 HLA-B27 positive patients (90.7%) and 36 HLA-B27 negative patients (9.3%). The ANOVA test indicated that HLA-B27 positive patients and male patients respectively had an earlier age at disease onset than HLA-B27 negative patients and female patients. The logistic regression analysis indicated that positive HLA-B27 status (OR 2.601, p=0.004) and male gender (OR 1.923, p=0.004) were significant predictors of worse sacroiliitis. In addition, elevated ESR (OR 2.181, p=0.013) and longer disease duration (OR 1.100, p<0.001) contributed to worse sacroiliitis likewise. Conclusion: Positive HLA-B27 status and male gender are associated with worse sacroiliitis on CT, acting as predictors of sacroiliitis. Elevated ESR and longer disease duration also contribute to worse sacroiliitis. Meanwhile, positive HLA-B27 status and male gender are associated with earlier age at disease onset.
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spelling pubmed-39555352014-03-17 Association of HLA-B27 status and gender with sacroiliitis in patients with ankylosing spondylitis Xiong, Jiangbiao Chen, Jing Tu, Jianxin Ye, Wenjing Zhang, Zhiyong Liu, Qiaoqiong Zhu, Xiaochun Pak J Med Sci Original Article Objective: To observe the influence of human leucocyte antigen B27 (HLA-B27) status and gender on sacroiliitis on computed tomography (CT) in ankylosingspondylitis (AS). Methods: We reviewed the archived medical records of the AS inpatients admitted in the Rheumatology Department of the First Affiliated Hospital of Wenzhou Medical University during the period from January 2007 through January 2013 and finally 386 patients were included in the study. The severity of sacroiliitis on CT was evaluated according to the grading used in the modified New York criteria for AS. Two-way classification analysis of variance (ANOVA) was employed to examine the effect of HLA-B27 status and gender on age at disease onset. The impact of HLA-B27 and gender on sacroiliitis on CT was tested by univariate and multivariate logistic regression analyses. Results: There were 350 HLA-B27 positive patients (90.7%) and 36 HLA-B27 negative patients (9.3%). The ANOVA test indicated that HLA-B27 positive patients and male patients respectively had an earlier age at disease onset than HLA-B27 negative patients and female patients. The logistic regression analysis indicated that positive HLA-B27 status (OR 2.601, p=0.004) and male gender (OR 1.923, p=0.004) were significant predictors of worse sacroiliitis. In addition, elevated ESR (OR 2.181, p=0.013) and longer disease duration (OR 1.100, p<0.001) contributed to worse sacroiliitis likewise. Conclusion: Positive HLA-B27 status and male gender are associated with worse sacroiliitis on CT, acting as predictors of sacroiliitis. Elevated ESR and longer disease duration also contribute to worse sacroiliitis. Meanwhile, positive HLA-B27 status and male gender are associated with earlier age at disease onset. Professional Medical Publicaitons 2014 /pmc/articles/PMC3955535/ /pubmed/24639824 http://dx.doi.org/10.12669/pjms.301.3896 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Xiong, Jiangbiao
Chen, Jing
Tu, Jianxin
Ye, Wenjing
Zhang, Zhiyong
Liu, Qiaoqiong
Zhu, Xiaochun
Association of HLA-B27 status and gender with sacroiliitis in patients with ankylosing spondylitis
title Association of HLA-B27 status and gender with sacroiliitis in patients with ankylosing spondylitis
title_full Association of HLA-B27 status and gender with sacroiliitis in patients with ankylosing spondylitis
title_fullStr Association of HLA-B27 status and gender with sacroiliitis in patients with ankylosing spondylitis
title_full_unstemmed Association of HLA-B27 status and gender with sacroiliitis in patients with ankylosing spondylitis
title_short Association of HLA-B27 status and gender with sacroiliitis in patients with ankylosing spondylitis
title_sort association of hla-b27 status and gender with sacroiliitis in patients with ankylosing spondylitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955535/
https://www.ncbi.nlm.nih.gov/pubmed/24639824
http://dx.doi.org/10.12669/pjms.301.3896
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