Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10113
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dc.contributor.authorRoberts, Matthew Aen
dc.contributor.authorThomas, Merlin Cen
dc.contributor.authorFernando, Dharshen
dc.contributor.authorMacmillan, Neilen
dc.contributor.authorPower, David Anthonyen
dc.contributor.authorIerino, Francesco Len
dc.date.accessioned2015-05-15T23:27:44Z
dc.date.available2015-05-15T23:27:44Z
dc.date.issued2006-03-06en
dc.identifier.citationNephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association 2006; 21(6): 1611-7en
dc.identifier.govdoc16520354en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/10113en
dc.description.abstractAdvanced glycation end products (AGEs) have biological properties that may contribute to the premature cardiovascular mortality of haemodialysis patients. This study examines the hypothesis that low molecular weight forms of fluorescent AGEs (LMW fluorescence) predict mortality in haemodialysis patients.The LMW fluorescence was measured in 85 patients treated with chronic haemodialysis and prospectively followed for 4 years. The primary outcome of all-cause mortality was assessed using Cox proportional hazards regression model.At the end of the follow-up period 37 (44%) patients died. The median LMW fluorescence level was 24.2 arbitrary units (range: 10.6-148.1 AU) and the receiver operator characteristic (ROC) curve cut-off for mortality was 37.0 AU. The LMW fluorescence predicted death both as a binary variable at the ROC cut-off, and as a continuous log-transformed variable when adjusted for age, albumin and C-reactive protein (CRP). Adjusted for age, albumin and CRP, the hazard ratio for mortality was 3.05 (1.41-6.60, P = 0.005) for LMW fluorescence as a binary variable and 2.71 per log unit (1.37-5.38, P = 0.004) as a continuous log-transformed variable.The low molecular weight forms of AGEs predict mortality in patients receiving chronic haemodialysis, and may be important in the mechanisms leading to atherosclerosis and inflammation in such patients.en
dc.language.isoenen
dc.subject.otherAgeden
dc.subject.otherCardiovascular Diseases.diagnosis.etiologyen
dc.subject.otherFemaleen
dc.subject.otherFluorescenceen
dc.subject.otherGlycosylation End Products, Advanced.blooden
dc.subject.otherHumansen
dc.subject.otherKidney Failure, Chronic.diagnosis.mortalityen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherMolecular Weighten
dc.subject.otherMortalityen
dc.subject.otherPredictive Value of Testsen
dc.subject.otherProspective Studiesen
dc.subject.otherROC Curveen
dc.subject.otherRenal Dialysisen
dc.titleLow molecular weight advanced glycation end products predict mortality in asymptomatic patients receiving chronic haemodialysis.en
dc.typeJournal Articleen
dc.identifier.journaltitleNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Associationen
dc.identifier.affiliationDepartment of Nephrology, Austin Health, Heidelberg 3084, Victoria, Australiaen
dc.identifier.doi10.1093/ndt/gfl053en
dc.description.pages1611-7en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/16520354en
dc.type.austinJournal Articleen
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
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