Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/108360
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dc.contributor.authorMarques, Andréa-
dc.contributor.authorLucas, Raquel-
dc.contributor.authorSimões, Eugénia-
dc.contributor.authorVerstappen, Suzanne M. M.-
dc.contributor.authorJacobs, Johannes W. G.-
dc.contributor.authorSilva, José A. P. da-
dc.date.accessioned2023-08-25T11:18:55Z-
dc.date.available2023-08-25T11:18:55Z-
dc.date.issued2017-
dc.identifier.issn2056-5933pt
dc.identifier.urihttps://hdl.handle.net/10316/108360-
dc.description.abstractObjective E valuate the performance of FRAX®, with and without bone mineral densitometry (BMD), in predicting the occurrence of fragility fractures over 10 years. Methods Participants aged ≥40 years at baseline, with a complete set of data and a minimum of 8.5 years of follow-up were identified from three cohorts (n=2626). Ten-year fracture risk at baseline were estimated with FRAX® and assessed by comparison with observed fractures and receiver operating characteristic analysis. Results During a mean (SD) follow-up of 9.12 (1.5) years, 178 participants suffered a major osteoporotic (MOP) fracture and 28 sustained a hip fracture. The predictive performance of FRAX® was superior to that of BMD alone for both MOP and hip fractures. The area under the curve (AUC) of FRAX® without BMD was 0.76 (95% CI 0.72 to 0.79) for MOP fractures and 0.78 (95% CI 0.69 to 0.86) for hip fractures. No significant improvements were found when BMD was added to clinical variables to predict either MOP (0.78, 95% CI 0.74 to 0.82, p=0.25) or hip fractures (0.79, 95% CI 0.69 to 0.89, p=0.72). A UCs for FRAX® (with and without BMD) were greater for men than for women. FRAX®, with and without BMD, tended to underestimate the number of MOP fractures and to overestimate the number of hip fractures in females. In men, the number of observed fractures were within the 95% CI of the number predicted, both with and without BMD. Conclusion FRAX® without BMD provided good fracture prediction. Adding BMD to FRAX® did not improve the performance of the tool in the general population.pt
dc.language.isoporpt
dc.publisherBMJ Publishing Grouppt
dc.relationunrestricted grants from the Direção Geral da Saúde and Amgenpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt
dc.subjectepidemiology; osteoporosis; outcomes researchpt
dc.titleDo we need bone mineral density to estimate osteoporotic fracture risk? A 10-year prospective multicentre validation studypt
dc.typearticle-
degois.publication.firstPagee000509pt
degois.publication.issue2pt
degois.publication.titleRMD Openpt
dc.peerreviewedyespt
dc.identifier.doi10.1136/rmdopen-2017-000509pt
degois.publication.volume3pt
dc.date.embargo2017-01-01*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1pt-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.orcid0000-0002-2782-6780-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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