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Trabecular Bone Score (TBS) in Patients with Early Ankylosing Spondylitis—Limited Utility
Purpose: Ankylosing spondylitis (AS) not only results in pathological ossification of the spine, but can also be associated with osteoporosis. Due to the presence of syndesmophytes and possible involvement of the hip joints, classical dual X-ray absorptiometry (DXA) is of limited use in patients wit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623295/ https://www.ncbi.nlm.nih.gov/pubmed/34830653 http://dx.doi.org/10.3390/jcm10225373 |
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author | Nowakowska-Płaza, Anna Wroński, Jakub Sudoł-Szopińska, Iwona Głuszko, Piotr |
author_facet | Nowakowska-Płaza, Anna Wroński, Jakub Sudoł-Szopińska, Iwona Głuszko, Piotr |
author_sort | Nowakowska-Płaza, Anna |
collection | PubMed |
description | Purpose: Ankylosing spondylitis (AS) not only results in pathological ossification of the spine, but can also be associated with osteoporosis. Due to the presence of syndesmophytes and possible involvement of the hip joints, classical dual X-ray absorptiometry (DXA) is of limited use in patients with advanced stages of AS. Trabecular bone score (TBS) is a method complementary to DXA, providing additional information about bone microarchitecture. There is a growing body of evidence for the usefulness of TBS in AS patients. The aim of this study was to assess the clinical utility of TBS in patients with AS. Methods: Patients with AS underwent DXA with additional TBS assessment. A cross-sectional analysis of the frequency of osteoporosis and bone microarchitecture deterioration and their association with patients’ characteristics was done. Results: A total of 51 male patients, mean age 40.7 years, were enrolled. Osteoporosis was diagnosed in seven patients (13.7%). Lumbar bone mineral density (BMD) was higher (p < 0.001) than femoral BMD, indicating abnormal BMD readings in the spine caused by syndesmophytes. Patients with DXA-diagnosed osteoporosis had lower TBS (p = 0.03) and TBS T-score (p = 0.043) values compared to patients without osteoporosis. However, disturbed bone microarchitecture (TBS < 1.23) was present in only three patients (5.9%). None of the patients had a history of an osteoporotic fracture. A lower TBS T-score (p = 0.032) was demonstrated in patients with sacroiliitis grade 4 than in patients with sacroiliitis grade 2, with no significant differences in BMD and T-score values. Conclusion: Among patients with early AS, the clinical utility of TBS is limited—it does not add value to DXA. |
format | Online Article Text |
id | pubmed-8623295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86232952021-11-27 Trabecular Bone Score (TBS) in Patients with Early Ankylosing Spondylitis—Limited Utility Nowakowska-Płaza, Anna Wroński, Jakub Sudoł-Szopińska, Iwona Głuszko, Piotr J Clin Med Article Purpose: Ankylosing spondylitis (AS) not only results in pathological ossification of the spine, but can also be associated with osteoporosis. Due to the presence of syndesmophytes and possible involvement of the hip joints, classical dual X-ray absorptiometry (DXA) is of limited use in patients with advanced stages of AS. Trabecular bone score (TBS) is a method complementary to DXA, providing additional information about bone microarchitecture. There is a growing body of evidence for the usefulness of TBS in AS patients. The aim of this study was to assess the clinical utility of TBS in patients with AS. Methods: Patients with AS underwent DXA with additional TBS assessment. A cross-sectional analysis of the frequency of osteoporosis and bone microarchitecture deterioration and their association with patients’ characteristics was done. Results: A total of 51 male patients, mean age 40.7 years, were enrolled. Osteoporosis was diagnosed in seven patients (13.7%). Lumbar bone mineral density (BMD) was higher (p < 0.001) than femoral BMD, indicating abnormal BMD readings in the spine caused by syndesmophytes. Patients with DXA-diagnosed osteoporosis had lower TBS (p = 0.03) and TBS T-score (p = 0.043) values compared to patients without osteoporosis. However, disturbed bone microarchitecture (TBS < 1.23) was present in only three patients (5.9%). None of the patients had a history of an osteoporotic fracture. A lower TBS T-score (p = 0.032) was demonstrated in patients with sacroiliitis grade 4 than in patients with sacroiliitis grade 2, with no significant differences in BMD and T-score values. Conclusion: Among patients with early AS, the clinical utility of TBS is limited—it does not add value to DXA. MDPI 2021-11-18 /pmc/articles/PMC8623295/ /pubmed/34830653 http://dx.doi.org/10.3390/jcm10225373 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nowakowska-Płaza, Anna Wroński, Jakub Sudoł-Szopińska, Iwona Głuszko, Piotr Trabecular Bone Score (TBS) in Patients with Early Ankylosing Spondylitis—Limited Utility |
title | Trabecular Bone Score (TBS) in Patients with Early Ankylosing Spondylitis—Limited Utility |
title_full | Trabecular Bone Score (TBS) in Patients with Early Ankylosing Spondylitis—Limited Utility |
title_fullStr | Trabecular Bone Score (TBS) in Patients with Early Ankylosing Spondylitis—Limited Utility |
title_full_unstemmed | Trabecular Bone Score (TBS) in Patients with Early Ankylosing Spondylitis—Limited Utility |
title_short | Trabecular Bone Score (TBS) in Patients with Early Ankylosing Spondylitis—Limited Utility |
title_sort | trabecular bone score (tbs) in patients with early ankylosing spondylitis—limited utility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623295/ https://www.ncbi.nlm.nih.gov/pubmed/34830653 http://dx.doi.org/10.3390/jcm10225373 |
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