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Bone mineral density and inflammatory bowel disease severity
Inflammatory bowel disease (IBD) is associated with low bone mineral density (BMD). In this study, the association between disease severity and BMD in patients with IBD was evaluated. Associations between BMD and the Montreal classification, disease activity and drug therapy were also tested. A cros...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649869/ https://www.ncbi.nlm.nih.gov/pubmed/29069227 http://dx.doi.org/10.1590/1414-431X20176374 |
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author | Lima, C.A. Lyra, A.C. Mendes, C.M.C. Lopes, M.B. Coqueiro, F.G. Rocha, R. Santana, G.O. |
author_facet | Lima, C.A. Lyra, A.C. Mendes, C.M.C. Lopes, M.B. Coqueiro, F.G. Rocha, R. Santana, G.O. |
author_sort | Lima, C.A. |
collection | PubMed |
description | Inflammatory bowel disease (IBD) is associated with low bone mineral density (BMD). In this study, the association between disease severity and BMD in patients with IBD was evaluated. Associations between BMD and the Montreal classification, disease activity and drug therapy were also tested. A cross-sectional prevalence study with a comparison group was conducted. One hundred and twenty-eight patients were evaluated: 68 patients with ulcerative colitis (UC), and 60 with Crohn's disease (CD). The control group consisted of 67 healthy subjects. All patients and controls had BMD measured and in IBD patients, current medications, hospitalization, and disease location, extent and phenotype, according to the Montreal classification, were recorded. Multiple correspondence analysis was applied to evaluate categorical variables. In the CD group, most patients were diagnosed between 17–40 years of age. Ileocolonic and non-stricturing non-penetrating disease were the most frequent disease location and behavior, respectively. In UC patients, extensive colitis was the most frequent disease location. UC and CD patients were more likely to have osteopenia than controls (OR=14.93/OR=24.38, respectively). In the CD group, male patients, perianal disease, penetrating behavior and age at diagnosis >40 years were associated with low BMD. Taking azathioprine and infliximab also seemed to be associated with osteopenia. In the UC group, we observed an association between low BMD and male patients, left colitis, corticosteroid use and hospitalization. Disease activity was not associated with osteopenia or osteoporosis in CD and UC patients. Disease severity seems to be associated with osteopenia in IBD patients. |
format | Online Article Text |
id | pubmed-5649869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-56498692017-10-31 Bone mineral density and inflammatory bowel disease severity Lima, C.A. Lyra, A.C. Mendes, C.M.C. Lopes, M.B. Coqueiro, F.G. Rocha, R. Santana, G.O. Braz J Med Biol Res Research Articles Inflammatory bowel disease (IBD) is associated with low bone mineral density (BMD). In this study, the association between disease severity and BMD in patients with IBD was evaluated. Associations between BMD and the Montreal classification, disease activity and drug therapy were also tested. A cross-sectional prevalence study with a comparison group was conducted. One hundred and twenty-eight patients were evaluated: 68 patients with ulcerative colitis (UC), and 60 with Crohn's disease (CD). The control group consisted of 67 healthy subjects. All patients and controls had BMD measured and in IBD patients, current medications, hospitalization, and disease location, extent and phenotype, according to the Montreal classification, were recorded. Multiple correspondence analysis was applied to evaluate categorical variables. In the CD group, most patients were diagnosed between 17–40 years of age. Ileocolonic and non-stricturing non-penetrating disease were the most frequent disease location and behavior, respectively. In UC patients, extensive colitis was the most frequent disease location. UC and CD patients were more likely to have osteopenia than controls (OR=14.93/OR=24.38, respectively). In the CD group, male patients, perianal disease, penetrating behavior and age at diagnosis >40 years were associated with low BMD. Taking azathioprine and infliximab also seemed to be associated with osteopenia. In the UC group, we observed an association between low BMD and male patients, left colitis, corticosteroid use and hospitalization. Disease activity was not associated with osteopenia or osteoporosis in CD and UC patients. Disease severity seems to be associated with osteopenia in IBD patients. Associação Brasileira de Divulgação Científica 2017-10-19 /pmc/articles/PMC5649869/ /pubmed/29069227 http://dx.doi.org/10.1590/1414-431X20176374 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Lima, C.A. Lyra, A.C. Mendes, C.M.C. Lopes, M.B. Coqueiro, F.G. Rocha, R. Santana, G.O. Bone mineral density and inflammatory bowel disease severity |
title | Bone mineral density and inflammatory bowel disease severity |
title_full | Bone mineral density and inflammatory bowel disease severity |
title_fullStr | Bone mineral density and inflammatory bowel disease severity |
title_full_unstemmed | Bone mineral density and inflammatory bowel disease severity |
title_short | Bone mineral density and inflammatory bowel disease severity |
title_sort | bone mineral density and inflammatory bowel disease severity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649869/ https://www.ncbi.nlm.nih.gov/pubmed/29069227 http://dx.doi.org/10.1590/1414-431X20176374 |
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