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dc.contributor.authorAlme, Katinka Nordheim
dc.date.accessioned2022-02-14T12:24:21Z
dc.date.available2022-02-14T12:24:21Z
dc.date.issued2022-03-01
dc.date.submitted2022-01-24T14:07:54.222Z
dc.identifiercontainer/5f/0e/29/47/5f0e2947-1442-482a-b72b-b470c87c4b0c
dc.identifier.isbn9788230858875
dc.identifier.isbn9788230866276
dc.identifier.urihttps://hdl.handle.net/11250/2978776
dc.description.abstractAbstract Background: Sedentary behaviour is associated with vascular disease, and being sedentary for long periods at a time is believed to be associated with the highest risk. The molecular mechanisms are presumed to follow metabolic and inflammatory pathways. Details about these pathways or the length of a clinical significant sedentary bout is not known. Aims: The primary aim of this study was to investigate the association between sedentary behaviour and novel blood biomarkers with potential predictive and explanatory properties. The secondary aim was to investigate the impact of sedentary behaviour bout length on these biomarkers. Materials and methods: Patients admitted to hospital for acute stroke were included in the multicentre cohort study entitled the Norwegian Cognitive Impairment After Stroke (Nor-COAST) study (n=815). At the three-month assessment (n=700), sedentary behaviour was measured using the body-worn sensor ActivPAL. Blood samples were drawn for analyses at the local laboratory directly, and biobank samples were stored and later analysed for inflammatory biomarkers at two research laboratories. The long-term outcomes, ischemic stroke recurrence and mortality was identified using national registries. Results: Glycated haemoglobin A (HbA1c) was positively associated with sedentary behaviour accumulated through bouts of 90 minutes or more. Total sedentary time was associated with higher levels of the inflammatory biomarkers C-reactive protein (CRP), interleukin-6 (IL-6), the pyridoxic acid ratio-index (PAr-index), and neopterin, and lower levels of kynurenic acid (KA). The study did not have enough power for investigating the impact of bout length on these biomarkers. There were no associations between the biomarkers and ischemic stroke recurrence. Mortality was associated with higher levels of CRP. When added to the same model, neopterin and KA showed positive and negative associations to mortality, respectively. Conclusion and implications: The results support that the impact of sedentary behaviour on disease progression is mediated through known vascular risk factors and novel biomarkers can be useful for future intervention studies.en_US
dc.language.isoengen_US
dc.publisherThe University of Bergenen_US
dc.relation.haspartPaper I: Alme KN, Knapskog AB, Næss H, Naik M, Beyer M, Ellekjaer H, English C, Ihle- Hansen H, Kummeneje CS, Munthe-Kaas R, Saltvedt I, Seljeseth Y, Tan X, Thingstad P, Askim T. “Is long-bout sedentary behaviour associated with long-term glucose levels three months after acute ischaemic stroke? A prospective observational cohort study.”. BMJ Open 2020; 10:e037475. The article is available in the thesis. The article is also available at: <a href="https://doi.org/10.1136/bmjopen-2020-037475" target="blank">https://doi.org/10.1136/bmjopen-2020-037475</a>en_US
dc.relation.haspartPaper II: Alme KN, Askim T, Assmus J, Mollnes TE, Naik M, Næss H, Saltvedt I, Ueland PM, Ulvik A, Knapskog AB. “Investigating novel biomarkers of immune activation and modulation in the context of sedentary behaviour: a multicentre prospective ischemic stroke cohort study.”. BMC Neurology 2021; 21:318. The article is available in the thesis. The article is also available at: <a href="https://doi.org/10.1186/s12883-021-02343-0" target="blank">https://doi.org/10.1186/s12883-021-02343-0</a>en_US
dc.relation.haspartPaper III: Alme KN, Ulvik A, Askim T, Assmus J, Mollnes TE, Naik M, Næss H, Saltvedt I, Ueland PM, Knapskog AB. “Neopterin and kynurenic acid as predictors of stroke recurrence and mortality. A multicentre prospective cohort study on biomarkers of inflammation measured three months after ischemic stroke.”. BMC Neurology 2021; 21:476. The article is available at: <a href="https://hdl.handle.net/11250/2929523" target="blank">https://hdl.handle.net/11250/2929523</a>en_US
dc.rightsAttribution (CC BY). This item's rights statement or license does not apply to the included articles in the thesis.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleSedentary behaviour and cerebrovascular disease: molecular mechanisms and the impact of bout duration. : A multicentre cohort study.en_US
dc.typeDoctoral thesisen_US
dc.date.updated2022-01-24T14:07:54.222Z
dc.rights.holderCopyright the Author.en_US
dc.contributor.orcid0000-0002-3925-4169
dc.description.degreeDoktorgradsavhandling
fs.unitcode13-24-0


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Attribution (CC BY). This item's rights statement or license does not apply to the included articles in the thesis.
Except where otherwise noted, this item's license is described as Attribution (CC BY). This item's rights statement or license does not apply to the included articles in the thesis.