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Clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset
We aimed to investigate the clinical, diagnostic, and imaging features of patients with late onset axial spondyloarthritis (SpA) with initial symptom manifestation aged over 45 years. Participants with axial SpA were consecutively recruited. Clinical, demographic, blood, and imaging parameters were...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302308/ https://www.ncbi.nlm.nih.gov/pubmed/35866796 http://dx.doi.org/10.1097/MD.0000000000029523 |
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author | Chung, Ho Yin Huang, Jin Xian Chan, Shirley Chiu Wai Lee, Kam Ho Tsang, Helen Hoi Lun Lau, Chak Sing |
author_facet | Chung, Ho Yin Huang, Jin Xian Chan, Shirley Chiu Wai Lee, Kam Ho Tsang, Helen Hoi Lun Lau, Chak Sing |
author_sort | Chung, Ho Yin |
collection | PubMed |
description | We aimed to investigate the clinical, diagnostic, and imaging features of patients with late onset axial spondyloarthritis (SpA) with initial symptom manifestation aged over 45 years. Participants with axial SpA were consecutively recruited. Clinical, demographic, blood, and imaging parameters were compared between the groups with early (≤45 years) and late onset (>45 years) at a cross-sectional level. Logistic regressions were used to determine the independent associations with axial SpA with late onset. A total of 455 participants were recruited. Among them, 70 (15.4%) had late onset disease. Multivariate analyses showed that axial SpA with late onset was associated with higher C-reactive protein based ankylosing spondylitis disease activity index (ASDAS-CRP) (B = 0.10; P = .04), higher intensity of spinal inflammation as measured by maximum apparent diffusion coefficient (spinal ADC max) (B = 0.27; P = .03) and mean ADC (spinal ADC mean) (B = 0.30; P = .004), lower modified Stoke Ankylosing Spondylitis Spinal Score (mSASSS) (B = –0.12; P = .02), more tender joint count (B = 0.12; P = .02), and fewer inflammatory back pain (IBP) (OR = 0.26; P < .001). Axial SpA with late onset had higher clinical disease activity, higher intensity of spinal MRI inflammation, less radiographic damage, and more tender joint count. There was also less inflammatory back pain, which could make the diagnosis more difficult. |
format | Online Article Text |
id | pubmed-9302308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-93023082022-08-03 Clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset Chung, Ho Yin Huang, Jin Xian Chan, Shirley Chiu Wai Lee, Kam Ho Tsang, Helen Hoi Lun Lau, Chak Sing Medicine (Baltimore) Research Article We aimed to investigate the clinical, diagnostic, and imaging features of patients with late onset axial spondyloarthritis (SpA) with initial symptom manifestation aged over 45 years. Participants with axial SpA were consecutively recruited. Clinical, demographic, blood, and imaging parameters were compared between the groups with early (≤45 years) and late onset (>45 years) at a cross-sectional level. Logistic regressions were used to determine the independent associations with axial SpA with late onset. A total of 455 participants were recruited. Among them, 70 (15.4%) had late onset disease. Multivariate analyses showed that axial SpA with late onset was associated with higher C-reactive protein based ankylosing spondylitis disease activity index (ASDAS-CRP) (B = 0.10; P = .04), higher intensity of spinal inflammation as measured by maximum apparent diffusion coefficient (spinal ADC max) (B = 0.27; P = .03) and mean ADC (spinal ADC mean) (B = 0.30; P = .004), lower modified Stoke Ankylosing Spondylitis Spinal Score (mSASSS) (B = –0.12; P = .02), more tender joint count (B = 0.12; P = .02), and fewer inflammatory back pain (IBP) (OR = 0.26; P < .001). Axial SpA with late onset had higher clinical disease activity, higher intensity of spinal MRI inflammation, less radiographic damage, and more tender joint count. There was also less inflammatory back pain, which could make the diagnosis more difficult. Lippincott Williams & Wilkins 2022-07-22 /pmc/articles/PMC9302308/ /pubmed/35866796 http://dx.doi.org/10.1097/MD.0000000000029523 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | Research Article Chung, Ho Yin Huang, Jin Xian Chan, Shirley Chiu Wai Lee, Kam Ho Tsang, Helen Hoi Lun Lau, Chak Sing Clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset |
title | Clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset |
title_full | Clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset |
title_fullStr | Clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset |
title_full_unstemmed | Clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset |
title_short | Clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset |
title_sort | clinical, radiological, and magnetic resonance imaging characteristics of axial spondyloarthritis with late onset |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302308/ https://www.ncbi.nlm.nih.gov/pubmed/35866796 http://dx.doi.org/10.1097/MD.0000000000029523 |
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