Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11718
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dc.contributor.authorRoberts, Matthew Aen
dc.contributor.authorVelkoska, Elenaen
dc.contributor.authorIerino, Francesco Len
dc.contributor.authorBurrell, Louise Men
dc.date.accessioned2015-05-16T01:20:36Z
dc.date.available2015-05-16T01:20:36Z
dc.date.issued2013-03-27en
dc.identifier.citationNephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association 2013; 28(9): 2287-94en
dc.identifier.govdoc23535224en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11718en
dc.description.abstractAngiotensin-converting enzyme 2 (ACE2) is a novel regulator of the renin-angiotensin system that counteracts the adverse effects of angiotensin II. In heart failure patients, elevated plasma ACE2 activity predicted adverse events and greater myocardial dysfunction. We aimed to describe plasma ACE2 activity and its clinical associations in patients with kidney disease.Patients recruited from a single centre comprised of chronic kidney disease Stage III/IV (CKD), haemodialysis patients and kidney transplant recipients (KTRs). Plasma ACE2 enzyme activity was measured using a fluorescent substrate assay in plasma, collected at baseline and stored at -80°C. Linear regression was performed in both males and females separately to determine the covariates associated with log-transformed ACE2.The median (interquartile range) plasma ACE2 activity in pmol/mL/min was 15.9 (8.4-26.1) in CKD (n = 59), 9.2 (3.9-18.2) in haemodialysis (n = 100) and 13.1 (5.7-21.9) in KTR (n = 80; P < 0.01). In male haemodialysis patients, ACE2 activity was 12.1 (6.8-19.6) compared with 4.4 (2.5-10.3) in females (P < 0.01). Log-transformed ACE2 plasma activity was associated with post-haemodialysis systolic blood pressure in females [β-coefficient 0.04, 95% confidence interval (95% CI) 0.01-0.06, P = 0.006]. In males, log-transformed ACE2 plasma activity was associated with B-type natriuretic peptide (β-coefficient 0.39, 95% CI 0.19-0.60, P < 0.001). Plasma ACE2 activity was not associated with mortality.Plasma ACE2 activity is reduced in haemodialysis patients compared with CKD patients, and in female haemodialysis patients compared with male. The different associations of plasma ACE2 activity between male and female haemodialysis patients indicate that the role of ACE2 in cardiovascular disease may differ by gender.en
dc.language.isoenen
dc.subject.otherangiotensin-converting enzyme 2en
dc.subject.othercardiovascular diseaseen
dc.subject.otherchronic dialysisen
dc.subject.otherchronic kidney diseaseen
dc.subject.otherend-stage kidney diseaseen
dc.subject.otherAgeden
dc.subject.otherBiological Markers.metabolismen
dc.subject.otherCohort Studiesen
dc.subject.otherCross-Sectional Studiesen
dc.subject.otherFemaleen
dc.subject.otherFollow-Up Studiesen
dc.subject.otherHumansen
dc.subject.otherKidney Transplantationen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherPeptidyl-Dipeptidase A.blooden
dc.subject.otherPrognosisen
dc.subject.otherRenal Dialysisen
dc.subject.otherRenal Insufficiency, Chronic.blood.enzymology.pathologyen
dc.titleAngiotensin-converting enzyme 2 activity in patients with chronic kidney disease.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, Melbourne, Australiaen
dc.identifier.doi10.1093/ndt/gft038en
dc.description.pages2287-94en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/23535224en
dc.type.austinJournal Articleen
local.name.researcherBurrell, Louise M
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptCardiology-
crisitem.author.deptGeneral Medicine-
crisitem.author.deptMedicine (University of Melbourne)-
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