Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/781
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dc.contributor.authorBeetham, Kassia S.en
dc.contributor.authorHowden, Erin J.en
dc.contributor.authorCoombes, Jeff S.en
dc.contributor.authorIsbel, Nicole M.en
dc.contributor.authorFadaee, Shannon B.en
dc.contributor.authorStanton, Tonyen
dc.date.accessioned2018-08-17T21:09:04Z-
dc.date.available2018-08-17T21:09:04Z-
dc.date.issued2017en
dc.identifier.citation22, (5), 2017, p. 197-204en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/781-
dc.description.abstractObjectives: Elevated oxidative stress and reduced heart rate variability (HRV) is prevalent in patients with chronic kidney disease (CKD) and is associated with increased morbidity and mortality. Previous studies have identified a positive association between elevated oxidative stress and autonomic dysfunction, however this relationship has not yet been investigated in the CKD population.; Methods: Plasma was collected from 78 patients with stage 3-4 CKD (estimated glomerular filtration rate 25-60 ml/min/1.73 m2) for the assessment of oxidative stress, including plasma total F2-isoprostanes, glutathione peroxidase activity and total antioxidant capacity. Time and frequency HRV parameters were measured from a three lead electrocardiogram.; Results: Participants with elevated F2-isoprostanes had reduced HRV compared to patients with normal levels of F2-isoprostanes. A number of HRV parameters were found to be inversely correlated with F2-isoprostanes in all CKD patients, including SDNN (r = -0.337; P < 0.01), VLF (r = -0.281, P = 0.01), LF (r = -0.315, P < 0.01) and total power (r = -0.288, P = 0.01). Multiple linear regression found F2-isoprostanes to be an independent predictor of SDNN (r2 = 0.287, β = -0.272, P = 0.01).; Discussion: Oxidative stress is significantly and independently associated with HRV in patients with CKD. Identifying oxidative stress in the pathogenesis of autonomic dysfunction may help target therapeutic strategies.;Date of Electronic Publication: 2016 Apr 19. Current Imprints: Publication: 2016- : Abingdon : Taylor & Francis; Original Imprints: Publication: Edinburgh ; New York : Churchill Livingstone, c1994- <br />en
dc.languageenen
dc.relation.ispartofRedox Report: Communications In Free Radical Researchen
dc.titleOxidative stress is associated with decreased heart rate variability in patients with chronic kidney diseaseen
dc.typeArticleen
dc.identifier.doi10.1080/13510002.2016.1173326en
dc.subject.keywordsOxidative Stress*/physiologyHeart Rate/*physiologyen
dc.subject.keywordsRenal Insufficiency, Chronic/*physiopathologyen
dc.subject.keywordsAgeden
dc.subject.keywordsAntioxidants/analysisen
dc.subject.keywordsCross-Sectional Studiesen
dc.subject.keywordsF2-Isoprostanes/blooden
dc.subject.keywordsFemaleen
dc.subject.keywordsGlutathione Peroxidase/blooden
dc.subject.keywordsHumansen
dc.subject.keywordsMaleen
dc.subject.keywordsMiddle Ageden
dc.subject.keywordsRegression Analysisen
dc.subject.keywordsRenal Insufficiency, Chronic/metabolismen
dc.subject.keywordsAutonomic dysfunctionen
dc.subject.keywordsChronic kidney diseaseen
dc.subject.keywordsHeart rate variabilityen
dc.subject.keywordsOxidative stressen
dc.relation.urlhttps://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=mdc&AN=27090392&site=ehost-liveen
dc.identifier.risid12en
dc.description.pages197-204en
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
Appears in Sites:Queensland Health Publications
West Moreton HHS Publications
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