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dc.contributor.authorLittle, Mark
dc.contributor.authorKenny, Rose
dc.contributor.authorCanney, Mark
dc.contributor.authorSexton, Donal J.
dc.contributor.authorO'Leary, Neil
dc.contributor.authorHealy, Martin
dc.contributor.authorO'Seaghdha, Conall M.
dc.date.accessioned2020-03-11T16:59:56Z
dc.date.available2020-03-11T16:59:56Z
dc.date.issued2018
dc.date.submitted2018en
dc.identifier.citationCanney, M., Sexton, D.J., O'Leary, N., Healy, M., Kenny, R.A., Little, M.A. & O'Seaghdha, C.M., Examining the utility of cystatin C as a confirmatory test of chronic kidney disease across the age range in middle-aged and older community-dwelling adults., Journal of epidemiology and community health, 72, 2018, 287-293en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstractBackground: Cystatin C has been proposed as a confirmatory test of chronic kidney disease (CKD). This is most applicable to older individuals with CKD, the majority of whom have a creatinine-based estimated glomerular filtration rate (eGFR) of 45–59 mL/min/1.73 m2 (CKD stage 3a). We sought to examine the utility of cystatin C as a confirmatory test of CKD across the age range in the general population of older adults. Methods: Cross-sectional analysis of 5386 participants from The Irish Longitudinal Study on Ageing, a cluster-sampled national cohort of community-dwelling adults aged ≥50 years. Cystatin C and creatinine were measured simultaneously using standardised assays. Using generalised additive models, we modelled the distributions of creatinine and cystatin C per year of age from four distributional parameters: location, dispersion, skewness, kurtosis. Among participants with CKD stage 3a, we estimated the predicted probability of cystatin C eGFR <60 mL/min/1.73 m2 (‘confirmed CKD’) as a function of age. Results: Median age was 62 years, 53% were female and median cystatin C eGFR was 80 mL/min/1.73 m2. We observed progressive variability in cystatin C with increasing age. Compared with creatinine, cystatin C levels rose sharply beyond the age of 65. Among participants with CKD stage 3a (n=463), the predicted probability of ‘confirmed CKD’ increased steadily with age, from 15% at age 50 to 80% at age 80. Conclusions: The clinical utility of cystatin C may be maximised in middle-aged individuals, in whom the distribution of cystatin C is less variable than older adults, and the pretest probability of confirming CKD is lower.en
dc.format.extent287-293en
dc.language.isoenen
dc.relation.ispartofseriesJournal of epidemiology and community health;
dc.relation.ispartofseries72;
dc.rightsYen
dc.subjectOlder adultsen
dc.subjectMiddle ageen
dc.subjectCystatin Cen
dc.subjectChronic kidney diseaseen
dc.titleExamining the utility of cystatin C as a confirmatory test of chronic kidney disease across the age range in middle-aged and older community-dwelling adultsen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/mlittle
dc.identifier.peoplefinderurlhttp://people.tcd.ie/rkenny
dc.identifier.rssinternalid182639
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0001-6003-397X
dc.identifier.urihttps://jech.bmj.com/content/72/4/287
dc.identifier.urihttp://hdl.handle.net/2262/91774


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