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FRAX®: Prediction of Major Osteoporotic Fractures in Women from the General Population: The OPUS Study

PURPOSES: The aim of this study was to analyse how well FRAX® predicts the risk of major osteoporotic and vertebral fractures over 6 years in postmenopausal women from general population. PATIENTS AND METHODS: The OPUS study was conducted in European women aged above 55 years, recruited in 5 centers...

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Autores principales: Briot, Karine, Paternotte, Simon, Kolta, Sami, Eastell, Richard, Felsenberg, Dieter, Reid, David M., Glüer, Claus-C., Roux, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875449/
https://www.ncbi.nlm.nih.gov/pubmed/24386199
http://dx.doi.org/10.1371/journal.pone.0083436
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author Briot, Karine
Paternotte, Simon
Kolta, Sami
Eastell, Richard
Felsenberg, Dieter
Reid, David M.
Glüer, Claus-C.
Roux, Christian
author_facet Briot, Karine
Paternotte, Simon
Kolta, Sami
Eastell, Richard
Felsenberg, Dieter
Reid, David M.
Glüer, Claus-C.
Roux, Christian
author_sort Briot, Karine
collection PubMed
description PURPOSES: The aim of this study was to analyse how well FRAX® predicts the risk of major osteoporotic and vertebral fractures over 6 years in postmenopausal women from general population. PATIENTS AND METHODS: The OPUS study was conducted in European women aged above 55 years, recruited in 5 centers from random population samples and followed over 6 years. The population for this study consisted of 1748 women (mean age 74.2 years) with information on incident fractures. 742 (43.1%) had a prevalent fracture; 769 (44%) and 155 (8.9%) of them received an antiosteoporotic treatment before and during the study respectively. We compared FRAX® performance with and without bone mineral density (BMD) using receiver operator characteristic (ROC) c-statistical analysis with ORs and areas under receiver operating characteristics curves (AUCs) and net reclassification improvement (NRI). RESULTS: 85 (4.9%) patients had incident major fractures over 6 years. FRAX® with and without BMD predicted these fractures with an AUC of 0.66 and 0.62 respectively. The AUC were 0.60, 0.66, 0.69 for history of low trauma fracture alone, age and femoral neck (FN) BMD and combination of the 3 clinical risk factors, respectively. FRAX® with and without BMD predicted incident radiographic vertebral fracture (n = 65) with an AUC of 0.67 and 0.65 respectively. NRI analysis showed a significant improvement in risk assignment when BMD is added to FRAX®. CONCLUSIONS: This study shows that FRAX® with BMD and to a lesser extent also without FN BMD predict major osteoporotic and vertebral fractures in the general population.
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spelling pubmed-38754492014-01-02 FRAX®: Prediction of Major Osteoporotic Fractures in Women from the General Population: The OPUS Study Briot, Karine Paternotte, Simon Kolta, Sami Eastell, Richard Felsenberg, Dieter Reid, David M. Glüer, Claus-C. Roux, Christian PLoS One Research Article PURPOSES: The aim of this study was to analyse how well FRAX® predicts the risk of major osteoporotic and vertebral fractures over 6 years in postmenopausal women from general population. PATIENTS AND METHODS: The OPUS study was conducted in European women aged above 55 years, recruited in 5 centers from random population samples and followed over 6 years. The population for this study consisted of 1748 women (mean age 74.2 years) with information on incident fractures. 742 (43.1%) had a prevalent fracture; 769 (44%) and 155 (8.9%) of them received an antiosteoporotic treatment before and during the study respectively. We compared FRAX® performance with and without bone mineral density (BMD) using receiver operator characteristic (ROC) c-statistical analysis with ORs and areas under receiver operating characteristics curves (AUCs) and net reclassification improvement (NRI). RESULTS: 85 (4.9%) patients had incident major fractures over 6 years. FRAX® with and without BMD predicted these fractures with an AUC of 0.66 and 0.62 respectively. The AUC were 0.60, 0.66, 0.69 for history of low trauma fracture alone, age and femoral neck (FN) BMD and combination of the 3 clinical risk factors, respectively. FRAX® with and without BMD predicted incident radiographic vertebral fracture (n = 65) with an AUC of 0.67 and 0.65 respectively. NRI analysis showed a significant improvement in risk assignment when BMD is added to FRAX®. CONCLUSIONS: This study shows that FRAX® with BMD and to a lesser extent also without FN BMD predict major osteoporotic and vertebral fractures in the general population. Public Library of Science 2013-12-30 /pmc/articles/PMC3875449/ /pubmed/24386199 http://dx.doi.org/10.1371/journal.pone.0083436 Text en © 2013 Briot et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Briot, Karine
Paternotte, Simon
Kolta, Sami
Eastell, Richard
Felsenberg, Dieter
Reid, David M.
Glüer, Claus-C.
Roux, Christian
FRAX®: Prediction of Major Osteoporotic Fractures in Women from the General Population: The OPUS Study
title FRAX®: Prediction of Major Osteoporotic Fractures in Women from the General Population: The OPUS Study
title_full FRAX®: Prediction of Major Osteoporotic Fractures in Women from the General Population: The OPUS Study
title_fullStr FRAX®: Prediction of Major Osteoporotic Fractures in Women from the General Population: The OPUS Study
title_full_unstemmed FRAX®: Prediction of Major Osteoporotic Fractures in Women from the General Population: The OPUS Study
title_short FRAX®: Prediction of Major Osteoporotic Fractures in Women from the General Population: The OPUS Study
title_sort frax®: prediction of major osteoporotic fractures in women from the general population: the opus study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875449/
https://www.ncbi.nlm.nih.gov/pubmed/24386199
http://dx.doi.org/10.1371/journal.pone.0083436
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