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Osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population
BACKGROUND: The risk of osteoporosis in patients with psoriatic arthritis (PsA) still remains unclear. The aim of this study was to investigate bone mineral density (BMD) at the hip and lumbar spine measured by dual-energy X-ray absorptiometry in patients with PsA. METHODS: From an outpatient clinic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045713/ https://www.ncbi.nlm.nih.gov/pubmed/30018797 http://dx.doi.org/10.1136/rmdopen-2017-000631 |
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author | Gulati, Agnete Malm Michelsen, Brigitte Diamantopoulos, Andreas Grandaunet, Berit Salvesen, Øyvind Kavanaugh, Arthur Hoff, Mari Haugeberg, Glenn |
author_facet | Gulati, Agnete Malm Michelsen, Brigitte Diamantopoulos, Andreas Grandaunet, Berit Salvesen, Øyvind Kavanaugh, Arthur Hoff, Mari Haugeberg, Glenn |
author_sort | Gulati, Agnete Malm |
collection | PubMed |
description | BACKGROUND: The risk of osteoporosis in patients with psoriatic arthritis (PsA) still remains unclear. The aim of this study was to investigate bone mineral density (BMD) at the hip and lumbar spine measured by dual-energy X-ray absorptiometry in patients with PsA. METHODS: From an outpatient clinic in southern Norway, 140 patients with PsA were consecutively recruited and assessed for osteoporosis as part of a prospective study from January 2013 to May 2014. An extensive data collection was performed including demographic data and measures reflecting disease activity and health status. RESULTS: Mean age was 52.4 years and 71 (50.7%) were women. Median disease duration was 7.8 years. The proportion of patients with low BMD (defined as Z score≤−1.0 SD) was comparable to the expected value of 16%, according to the normal distribution of the Z score in the population. Osteoporosis was only found in 6.4% (95% CI3% to 11%) of the patients. No significant associations were found between BMD and disease activity measures. CONCLUSION: The prevalence of PsA patients with osteoporosis or low BMD was low and in the range seen in the reference population. This supports that patients with PsA are not at high risk for osteoporosis compared with the general population. Therefore, clinicians may follow the general population guidelines for monitoring of osteoporosis for patients with PsA. |
format | Online Article Text |
id | pubmed-6045713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-60457132018-07-17 Osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population Gulati, Agnete Malm Michelsen, Brigitte Diamantopoulos, Andreas Grandaunet, Berit Salvesen, Øyvind Kavanaugh, Arthur Hoff, Mari Haugeberg, Glenn RMD Open Psoriatic Arthritis BACKGROUND: The risk of osteoporosis in patients with psoriatic arthritis (PsA) still remains unclear. The aim of this study was to investigate bone mineral density (BMD) at the hip and lumbar spine measured by dual-energy X-ray absorptiometry in patients with PsA. METHODS: From an outpatient clinic in southern Norway, 140 patients with PsA were consecutively recruited and assessed for osteoporosis as part of a prospective study from January 2013 to May 2014. An extensive data collection was performed including demographic data and measures reflecting disease activity and health status. RESULTS: Mean age was 52.4 years and 71 (50.7%) were women. Median disease duration was 7.8 years. The proportion of patients with low BMD (defined as Z score≤−1.0 SD) was comparable to the expected value of 16%, according to the normal distribution of the Z score in the population. Osteoporosis was only found in 6.4% (95% CI3% to 11%) of the patients. No significant associations were found between BMD and disease activity measures. CONCLUSION: The prevalence of PsA patients with osteoporosis or low BMD was low and in the range seen in the reference population. This supports that patients with PsA are not at high risk for osteoporosis compared with the general population. Therefore, clinicians may follow the general population guidelines for monitoring of osteoporosis for patients with PsA. BMJ Publishing Group 2018-06-17 /pmc/articles/PMC6045713/ /pubmed/30018797 http://dx.doi.org/10.1136/rmdopen-2017-000631 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Psoriatic Arthritis Gulati, Agnete Malm Michelsen, Brigitte Diamantopoulos, Andreas Grandaunet, Berit Salvesen, Øyvind Kavanaugh, Arthur Hoff, Mari Haugeberg, Glenn Osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population |
title | Osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population |
title_full | Osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population |
title_fullStr | Osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population |
title_full_unstemmed | Osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population |
title_short | Osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population |
title_sort | osteoporosis in psoriatic arthritis: a cross-sectional study of an outpatient clinic population |
topic | Psoriatic Arthritis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045713/ https://www.ncbi.nlm.nih.gov/pubmed/30018797 http://dx.doi.org/10.1136/rmdopen-2017-000631 |
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