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dc.contributorDepartment of Rehabilitation Sciencesen_US
dc.creatorBorschmann, Ken_US
dc.creatorIuliano, Sen_US
dc.creatorGhasem-Zadeh, Aen_US
dc.creatorChurilov, Len_US
dc.creatorPang, MYCen_US
dc.creatorBernhardt, Jen_US
dc.date.accessioned2018-07-30T08:27:08Z-
dc.date.available2018-07-30T08:27:08Z-
dc.identifier.issn1862-3522en_US
dc.identifier.urihttp://hdl.handle.net/10397/77248-
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.rights© The Author(s) 2018. This article is an open access publicationen_US
dc.rightsOpen Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http:/ /creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.en_US
dc.rightsThe following publication Borschmann, K., Iuliano, S., Ghasem-Zadeh, A. et al. Upright activity and higher motor function may preserve bone mineral density within 6 months of stroke: a longitudinal study. Arch Osteoporos 13, 5 (2018) is available at https://doi.org/10.1007/s11657-017-0414-4.en_US
dc.subjectBone lossen_US
dc.subjectBone mineral densityen_US
dc.subjectHR-pQCTen_US
dc.subjectMicrostructureen_US
dc.subjectPhysical activityen_US
dc.subjectStrokeen_US
dc.titleUpright activity and higher motor function may preserve bone mineral density within 6 months of stroke : a longitudinal studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume13en_US
dc.identifier.issue1en_US
dc.identifier.doi10.1007/s11657-017-0414-4en_US
dcterms.abstractPurpose: Bone fragility contributes to increased fracture risk, but little is known about the emergence of post-stroke bone loss. We investigated skeletal changes and relationships with physical activity, stroke severity, motor control and lean mass within 6 months of stroke.en_US
dcterms.abstractMethods: This is a prospective observational study. Participants were non-diabetic but unable to walk within 2 weeks of first stroke. Distal tibial volumetric bone mineral density (vBMD, primary outcome), bone geometry and microstructure (high-resolution peripheral quantitative computed tomography) were assessed at baseline and 6 months, as were secondary outcomes total body bone mineral content and lean mass (dual energy X-ray absorptiometry), bone metabolism (serum osteocalcin, N-terminal propeptide of type 1 procollagen (P1NP), C-terminal telopeptide of type 1 collagen (CTX)), physical activity (PAL2 accelerometer) and motor control (Chedoke McMaster) which were also measured at 1 and 3 months.en_US
dcterms.abstractResults: Thirty-seven participants (69.7 years (SD 11.6), 37.8% females, NIHSS 12.6 (SD 4.7)) were included. The magnitude of difference in vBMD between paretic and non-paretic legs increased within 6 months, with a greater reduction observed in paretic legs (mean difference = 1.5% (95% CI 0.5, 2.6), p = 0.007). At 6 months, better motor control was associated with less bone loss since stroke (r = 0.46, p = 0.02). A trend towards less bone loss was observed in people who regained independent walking compared to those who did not (p = 0.053). Higher baseline daily count of standing up was associated with less change in bone turnover over 6 months: osteocalcin (r = −0.51, p = 0.01), P1NP (r = −0.47, p = 0.01), CTX (r = −0.53, p = 0.01).en_US
dcterms.abstractConclusion: Better motor control and walking recovery were associated with reduced bone loss. Interventions targeting these impairments from early post-stroke are warranted.en_US
dcterms.abstractClinical trial registration: URL: http://www.anzctr.org.au. Unique identifier: ACTRN12612000123842.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationArchives of osteoporosis, 2018, v. 13, no. 15en_US
dcterms.isPartOfArchives of osteoporosisen_US
dcterms.issued2018-
dc.identifier.scopus2-s2.0-85040222471-
dc.identifier.eissn1862-3514en_US
dc.identifier.artn5en_US
dc.identifier.rosgroupid2017000800-
dc.description.ros2017-2018 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validate201807 bcrcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberRS-0253-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextAustralian Research Council (ARCFT09901086), Austin Health Medical Research Fund and La Trobe University Faculty Research Grant.en_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6811353-
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