Näytä suppeat kuvailutiedot

dc.contributor.authorMäättä, Mikko
dc.contributor.authorMoilanen, Petro
dc.contributor.authorTimonen, Jussi
dc.contributor.authorPulkkinen, Pasi
dc.contributor.authorKorpelainen, Raija
dc.contributor.authorJämsä, Timo
dc.date.accessioned2014-08-13T10:03:44Z
dc.date.available2014-08-13T10:03:44Z
dc.date.issued2014
dc.identifier.citationMäättä, M., Moilanen, P., Timonen, J., Pulkkinen, P., Korpelainen, R., & Jämsä, T. (2014). Association between low-frequency ultrasound and hip fractures - comparison with DXA-based BMD. <i>BMC Musculoskeletal Disorders</i>, <i>15</i>(208). <a href="https://doi.org/10.1186/1471-2474-15-208" target="_blank">https://doi.org/10.1186/1471-2474-15-208</a>
dc.identifier.otherCONVID_23676293
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/44005
dc.description.abstractBackground: New methods for diagnosing osteoporosis and evaluating fracture risk are being developed. We aim to study the association between low-frequency (LF) axial transmission ultrasound and hip fracture risk in a population-based sample of older women. Methods: The study population consisted of 490 community-dwelling women (78 – 82 years). Ultrasound velocity (V LF ) at mid-tibia was measured in 2006 using a low-frequency scanning axial transmission device. Bone mineral density (BMD) at proximal femur measured using dual-energy x-ray absorptiometry (DXA) was used as the reference method. The fracture history of the participants was collected from December 1997 until the end of 2010. Lifestyle-related risk factors and mobility were assessed at 1997. Results: During the total follow-up period (1997 – 2010), 130 women had one or more fractures, and 20 of them had a hip fracture. Low V LF (the lowest quartile) was associated with increased hip fracture risk when compared with V LF in the normal range (Odds ratio, OR = 3.3, 95% confidence interval (CI) 1.3-8.4). However, V LF was not related to fracture risk when all bone sites were considered. Osteoporotic femoral neck BMD was associated with higher risk of a hip fracture (OR = 4.1, 95% CI 1.6-10.5) and higher risk of any fracture (OR = 2.4, 95% CI 1.6-3.8) compared to the non-osteoporotic femoral neck BMD. Decreased V LF remained a significant risk factor for hip fracture when combined with lifestyle-related risk factors (OR = 3.3, 95% CI 1.2-9.0). Conclusion: Low V LF was associated with hip fracture risk in older women even when combined with lifestyle-related risk factors. Further development of the method is needed to improve the measurement precision and to confirm the results.fi
dc.language.isoeng
dc.publisherBioMed Central Ltd.
dc.relation.ispartofseriesBMC Musculoskeletal Disorders
dc.relation.urihttp://www.biomedcentral.com/1471-2474/15/208
dc.subject.otherquantitative ultrasound
dc.subject.otherhip fracture
dc.subject.othercortical bone
dc.titleAssociation between low-frequency ultrasound and hip fractures - comparison with DXA-based BMD
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-201408132348
dc.contributor.laitosFysiikan laitosfi
dc.contributor.laitosDepartment of Physicsen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2014-08-13T03:32:21Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn1471-2474
dc.relation.numberinseries208
dc.relation.volume15
dc.type.versionpublishedVersion
dc.rights.copyright© 2014 Määttä et al.; licensee BioMed Central Ltd. 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 work is properly credited
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.subject.ysoäänennopeus
dc.subject.ysoosteoporoosi
jyx.subject.urihttp://www.yso.fi/onto/yso/p20764
jyx.subject.urihttp://www.yso.fi/onto/yso/p10781
dc.rights.urlhttp://creativecommons.org/licenses/by/2.0
dc.relation.doi10.1186/1471-2474-15-208
dc.type.okmA1


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Näytä suppeat kuvailutiedot

© 2014 Määttä et al.; licensee BioMed Central Ltd.

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 work is properly credited
Ellei muuten mainita, aineiston lisenssi on © 2014 Määttä et al.; licensee BioMed Central Ltd. 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 work is properly credited