Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12256
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dc.contributor.authorSinclair, Marie-
dc.contributor.authorAngus, Peter W-
dc.contributor.authorGow, Paul J-
dc.contributor.authorHoermann, Rudolf-
dc.contributor.authorMogilevski, Tamara-
dc.contributor.authorGrossmann, Mathis-
dc.date.accessioned2015-05-16T01:54:58Z
dc.date.available2015-05-16T01:54:58Z
dc.date.issued2014-10-15-
dc.identifier.citationTransplantation; 98(7): 788-92en_US
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12256en
dc.description.abstractLow pretransplant serum testosterone has recently been associated with increased mortality in men awaiting liver transplantation, but the potential impact on rejection has not yet been investigated.Pretransplantation serum testosterone, SHBG, and other variables were collected on 190 consecutive men who received a liver transplant between 2007 and 2013. Rates of subsequent acute cellular rejection were recorded. Multivariable analysis was performed to define variables associated with rejection and other clinically important end points.Thirty (16%) of 190 men experienced acute cellular rejection. Lower pretransplant testosterone was associated with lower rejection rates, -7% (95% confidence interval [CI], -2% to -12%) per nmol/L decrease in total testosterone and -4% (95% CI, -0.5% to -7%) per 10 pmol/L decrease in free testosterone. Total testosterone (correlation 0.29, P=0.04) and free testosterone (correlation 0.37, P=0.01) correlated significantly with the histological severity of rejection. Older age at transplant (+5% [95% CI, 9%-2%]) per year, and nonautoimmune etiology of liver disease (OR, 1.0 for autoimmune, 0.22 [95% CI, 0.07-0.73] for hepatitis C virus, and 0.58 [95% CI, 0.21-1.71] for other etiologies) were also associated with decreased rejection risk. In a generalized linear model including the covariates testosterone, SHBG, age, etiology, and MELD, total testosterone remained a significant predictor of rejection (adjusted OR, 1.06; P=0.03), as did age at transplant (OR, 0.95; P=0.01).Low preliver transplant serum testosterone independently predicts a decreased risk of acute allograft rejection. Whether testosterone is a marker of disease-associated immune dysfunction or has immune-modulatory effects requires further study.en_US
dc.language.isoenen
dc.subject.otherAdulten
dc.subject.otherAllograftsen
dc.subject.otherBiological Markers.blooden
dc.subject.otherDatabases, Factualen
dc.subject.otherEnd Stage Liver Disease.blood.surgeryen
dc.subject.otherGraft Rejection.blooden
dc.subject.otherHumansen
dc.subject.otherImmunosuppressive Agents.therapeutic useen
dc.subject.otherLength of Stayen
dc.subject.otherLiver.pathologyen
dc.subject.otherLiver Transplantationen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherMultivariate Analysisen
dc.subject.otherSeverity of Illness Indexen
dc.subject.otherTestosterone.blooden
dc.subject.otherTreatment Outcomeen
dc.titleLow-serum testosterone levels pre-liver transplantation are associated with reduced rates of early acute allograft rejection in men.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleTransplantationen_US
dc.identifier.affiliationVictorian Liver Transplant Uniten_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.doi10.1097/TP.0000000000000130en_US
dc.description.pages788-92en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/24918618en
dc.type.contentTexten_US
dc.type.austinJournal Articleen
local.name.researcherAngus, Peter W
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptEndocrinology-
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