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Risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis
INTRODUCTION: Although osteoporosis has been reported to be more common in patients with rheumatoid arthritis (RA), little is known whether the risk of osteoporotic fractures in these patients differs by age, sex, and anatomic site. METHODS: A retrospective cohort study was conducted using a health...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945054/ https://www.ncbi.nlm.nih.gov/pubmed/20682035 http://dx.doi.org/10.1186/ar3107 |
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author | Kim, Seo Young Schneeweiss, Sebastian Liu, Jun Daniel, Gregory W Chang, Chun-Lan Garneau, Katie Solomon, Daniel H |
author_facet | Kim, Seo Young Schneeweiss, Sebastian Liu, Jun Daniel, Gregory W Chang, Chun-Lan Garneau, Katie Solomon, Daniel H |
author_sort | Kim, Seo Young |
collection | PubMed |
description | INTRODUCTION: Although osteoporosis has been reported to be more common in patients with rheumatoid arthritis (RA), little is known whether the risk of osteoporotic fractures in these patients differs by age, sex, and anatomic site. METHODS: A retrospective cohort study was conducted using a health care utilization database. Incidence rates (IRs) and rate ratios (RRs) of osteoporotic fractures with 95% confidence intervals (CIs) were calculated. Multivariable Cox proportional hazards models compared the risk of osteoporotic fracture at typical sites between RA and non-RA patients. RESULTS: During a median 1.63-year follow-up, 872 (1.9%) of 47,034 RA patients experienced a fracture. The IR for osteoporotic fracture at typical sites among RA patients was 9.6 per 1,000 person-years, 1.5 times higher than the rate of non-RA patients. The IR was highest for hip fracture (3.4 per 1,000 person-years) in RA. The IRs across all age groups were higher for women than men and increased with older age in both groups. The RRs were elevated in RA patients across all common sites of osteoporotic fracture: hip (1.62, 95% CI 1.43 to 1.84), wrist (1.15, 95% CI 1.00 to 1.32), pelvis (2.02, 95% CI 1.77 to 2.30), and humerus (1.51, 95% CI 1.27 to 1.84). After confounding adjustment, a modest increase in risk for fracture was noted with RA (hazard ratio 1.26, 95% CI 1.15 to 1.38). CONCLUSIONS: Our study showed an increased risk of osteoporotic fractures for RA patients across all age groups, sex and various anatomic sites, compared with non-RA patients. |
format | Text |
id | pubmed-2945054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29450542010-09-25 Risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis Kim, Seo Young Schneeweiss, Sebastian Liu, Jun Daniel, Gregory W Chang, Chun-Lan Garneau, Katie Solomon, Daniel H Arthritis Res Ther Research Article INTRODUCTION: Although osteoporosis has been reported to be more common in patients with rheumatoid arthritis (RA), little is known whether the risk of osteoporotic fractures in these patients differs by age, sex, and anatomic site. METHODS: A retrospective cohort study was conducted using a health care utilization database. Incidence rates (IRs) and rate ratios (RRs) of osteoporotic fractures with 95% confidence intervals (CIs) were calculated. Multivariable Cox proportional hazards models compared the risk of osteoporotic fracture at typical sites between RA and non-RA patients. RESULTS: During a median 1.63-year follow-up, 872 (1.9%) of 47,034 RA patients experienced a fracture. The IR for osteoporotic fracture at typical sites among RA patients was 9.6 per 1,000 person-years, 1.5 times higher than the rate of non-RA patients. The IR was highest for hip fracture (3.4 per 1,000 person-years) in RA. The IRs across all age groups were higher for women than men and increased with older age in both groups. The RRs were elevated in RA patients across all common sites of osteoporotic fracture: hip (1.62, 95% CI 1.43 to 1.84), wrist (1.15, 95% CI 1.00 to 1.32), pelvis (2.02, 95% CI 1.77 to 2.30), and humerus (1.51, 95% CI 1.27 to 1.84). After confounding adjustment, a modest increase in risk for fracture was noted with RA (hazard ratio 1.26, 95% CI 1.15 to 1.38). CONCLUSIONS: Our study showed an increased risk of osteoporotic fractures for RA patients across all age groups, sex and various anatomic sites, compared with non-RA patients. BioMed Central 2010 2010-08-03 /pmc/articles/PMC2945054/ /pubmed/20682035 http://dx.doi.org/10.1186/ar3107 Text en Copyright ©2010 Kim 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 Kim, Seo Young Schneeweiss, Sebastian Liu, Jun Daniel, Gregory W Chang, Chun-Lan Garneau, Katie Solomon, Daniel H Risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis |
title | Risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis |
title_full | Risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis |
title_fullStr | Risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis |
title_full_unstemmed | Risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis |
title_short | Risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis |
title_sort | risk of osteoporotic fracture in a large population-based cohort of patients with rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945054/ https://www.ncbi.nlm.nih.gov/pubmed/20682035 http://dx.doi.org/10.1186/ar3107 |
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