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Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis
INTRODUCTION: The aim of the present study was to compare bone mineral density (BMD) and body composition (BC) measurements as well as identify risk factors for low BMD and osteoporotic fractures in postmenopausal women with psoriasis (Ps) and psoriatic arthritis (PsA). METHODS: A cross-sectional st...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241360/ https://www.ncbi.nlm.nih.gov/pubmed/21299865 http://dx.doi.org/10.1186/ar3240 |
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author | Pedreira, Paulo G Pinheiro, Marcelo M Szejnfeld, Vera L |
author_facet | Pedreira, Paulo G Pinheiro, Marcelo M Szejnfeld, Vera L |
author_sort | Pedreira, Paulo G |
collection | PubMed |
description | INTRODUCTION: The aim of the present study was to compare bone mineral density (BMD) and body composition (BC) measurements as well as identify risk factors for low BMD and osteoporotic fractures in postmenopausal women with psoriasis (Ps) and psoriatic arthritis (PsA). METHODS: A cross-sectional study was carried out in 45 PsA women, 52 Ps women and 98 healthy female controls (HC). Clinical risk factors for low bone density and osteoporotic fracture were evaluated by a specific questionnaire. An X-ray absorptiometry (DXA) at the lumbar spine, total femur and total body was performed on all patients. Skin and joint outcomes were measured by specific tools (PASI, HAQ and DAS28). Morphometric vertebral fractures were evaluated by lumbar and thoracic spine X-ray, according to Genant's method. RESULTS: There were no significant differences in age, body mass index (BMI), total lean mass and bone mineral density among the groups. However, the PsA group had a significantly higher body fat percentage (BF%) than the Ps and HC groups. Osteoporotic fractures were more frequently observed in PsA and Ps groups than in the HC group (P = 0.01). Recurrent falls and a longer duration of disease increased the risk of fracture (odds ratio (OR) = 18.3 and 1.08, respectively) in the PsA group (P = 0.02). Disability was the main factor related to osteoporotic fracture in the Ps group (odds ratio (OR) = 11.1) (P = 0.02). CONCLUSIONS: Ps and PsA patients did not present lower BMD. However, they had a higher prevalence of osteoporotic fractures and higher risk of metabolic syndrome. Patients with a longer duration of disease, disability and recurrent falls need preventive measures. |
format | Online Article Text |
id | pubmed-3241360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32413602011-12-17 Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis Pedreira, Paulo G Pinheiro, Marcelo M Szejnfeld, Vera L Arthritis Res Ther Research Article INTRODUCTION: The aim of the present study was to compare bone mineral density (BMD) and body composition (BC) measurements as well as identify risk factors for low BMD and osteoporotic fractures in postmenopausal women with psoriasis (Ps) and psoriatic arthritis (PsA). METHODS: A cross-sectional study was carried out in 45 PsA women, 52 Ps women and 98 healthy female controls (HC). Clinical risk factors for low bone density and osteoporotic fracture were evaluated by a specific questionnaire. An X-ray absorptiometry (DXA) at the lumbar spine, total femur and total body was performed on all patients. Skin and joint outcomes were measured by specific tools (PASI, HAQ and DAS28). Morphometric vertebral fractures were evaluated by lumbar and thoracic spine X-ray, according to Genant's method. RESULTS: There were no significant differences in age, body mass index (BMI), total lean mass and bone mineral density among the groups. However, the PsA group had a significantly higher body fat percentage (BF%) than the Ps and HC groups. Osteoporotic fractures were more frequently observed in PsA and Ps groups than in the HC group (P = 0.01). Recurrent falls and a longer duration of disease increased the risk of fracture (odds ratio (OR) = 18.3 and 1.08, respectively) in the PsA group (P = 0.02). Disability was the main factor related to osteoporotic fracture in the Ps group (odds ratio (OR) = 11.1) (P = 0.02). CONCLUSIONS: Ps and PsA patients did not present lower BMD. However, they had a higher prevalence of osteoporotic fractures and higher risk of metabolic syndrome. Patients with a longer duration of disease, disability and recurrent falls need preventive measures. BioMed Central 2011 2011-02-07 /pmc/articles/PMC3241360/ /pubmed/21299865 http://dx.doi.org/10.1186/ar3240 Text en Copyright ©2011 Pedreira et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Pedreira, Paulo G Pinheiro, Marcelo M Szejnfeld, Vera L Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis |
title | Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis |
title_full | Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis |
title_fullStr | Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis |
title_full_unstemmed | Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis |
title_short | Bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis |
title_sort | bone mineral density and body composition in postmenopausal women with psoriasis and psoriatic arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241360/ https://www.ncbi.nlm.nih.gov/pubmed/21299865 http://dx.doi.org/10.1186/ar3240 |
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