Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/72132
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dc.contributorDepartment of Rehabilitation Sciencesen_US
dc.creatorBorschmann, KNen_US
dc.creatorEkinci, EIen_US
dc.creatorIuliano, Sen_US
dc.creatorChurilov, Len_US
dc.creatorPang, MYCen_US
dc.creatorBernhardt, Jen_US
dc.date.accessioned2018-01-31T01:16:19Z-
dc.date.available2018-01-31T01:16:19Z-
dc.identifier.issn2396-9873en_US
dc.identifier.urihttp://hdl.handle.net/10397/72132-
dc.language.isoenen_US
dc.publisherSAGE Publicationsen_US
dc.rightsThis is the accepted version of the publication Borschmann KN, Ekinci EI, Iuliano S, Churilov L, Pang MY, Bernhardt J. Reducing sedentary time and fat mass may improve glucose tolerance and insulin sensitivity in adults surviving 6 months after stroke: A phase I pilot study. European Stroke Journal (Volume: 2 issue: 2) pp. 144-153. Copyright © 2017 (European Stroke Organisation). DOI: 10.1177/2396987317694469.en_US
dc.subjectStrokeen_US
dc.subjectGlycaemic controlen_US
dc.subjectPhysical activityen_US
dc.subjectBody compositionen_US
dc.titleReducing sedentary time and fat mass may improve glucose tolerance and insulin sensitivity in adults surviving 6 months after stroke : a phase I pilot studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage144en_US
dc.identifier.epage153en_US
dc.identifier.volume2en_US
dc.identifier.issue2en_US
dc.identifier.doi10.1177/2396987317694469en_US
dcterms.abstractIntroduction: Deranged glycaemic control is common post-stroke, increasing risks of recurrent stroke and development of diabetes. The aim of the study is to examine glucose metabolism in relation to body composition, physical activity and sedentary time post-stroke.en_US
dcterms.abstractPatients and methods: Observational study: Non-diabetic adults, unable to walk independently, were recruited within 2 weeks of first stroke. Primary outcome: 2-h glucose level (mmol/l, oral glucose tolerance test), assessed at baseline and 6 months. Homeostasis Model Assessment of Insulin Sensitivity, total body fat and lean mass (dual energy X-ray absorptiometry), sedentary time (lying or sitting), standing and walking (PAL2 accelerometer) were assessed at baseline, 1, 3 and 6 months. Generalised estimating equations were used to examine change over time and associations between outcome measures.en_US
dcterms.abstractResults: Thirty-six participants (69.5 years (standard deviation 11.7), 13 (36.1%) female, moderate stroke severity (National Institute of Health Stroke Scale 11.5 (interquartile range 9.75, 16)). Within 6 months, adjusting for age and National Institute of Health Stroke Scale, every month 2-h glucose reduced by 4.5% (p < 0.001), Homeostasis Model Assessment of Insulin Sensitivity improved 3% (p = 0.04) and fat mass decreased 490 g (95% confidence interval 325, 655; p = 0.01). For every extra kilogram of body fat, 2-h glucose increased by 1.02 mmol/L (95% confidence interval 1.01, 1.02; p = 0.001); Homeostasis Model Assessment of Insulin Sensitivity reduced by 0.98% (95% confidence interval 0.97, 0.99; p = 0.001). Time spent sedentary reduced from 98.5% of measurement period (interquartile range 94.3, 99.8) to 74.3% (interquartile range 65.5, 88.6), by 2.8% monthly (95% confidence interval 1.8, 3.9, p < 0.001). For every additional 5% sedentary time, 2-h glucose increased by 1.05 mmol/L (95% confidence interval 1.04, 1.07; p < 0.001).en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationEuropean stroke journal, 1 June 2017, v. 2, no. 2, p. 144-153en_US
dcterms.isPartOfEuropean stroke journalen_US
dcterms.issued2017-06-01-
dc.identifier.ros2016001909-
dc.identifier.eissn2396-9881en_US
dc.identifier.rosgroupid2016001873-
dc.description.ros2016-2017 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validatebcmaen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberRS-0386-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextthe Operational Infrastructure Support Granten_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS22831921-
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