dc.contributor.author | Little, Mark | |
dc.contributor.author | Kenny, Rose | |
dc.contributor.author | Canney, Mark | |
dc.contributor.author | Sexton, Donal J. | |
dc.contributor.author | O'Leary, Neil | |
dc.contributor.author | Healy, Martin | |
dc.contributor.author | O'Seaghdha, Conall M. | |
dc.date.accessioned | 2020-03-11T16:59:56Z | |
dc.date.available | 2020-03-11T16:59:56Z | |
dc.date.issued | 2018 | |
dc.date.submitted | 2018 | en |
dc.identifier.citation | Canney, 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, 287-293 | en |
dc.identifier.other | Y | |
dc.description | PUBLISHED | en |
dc.description.abstract | Background: 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.extent | 287-293 | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Journal of epidemiology and community health; | |
dc.relation.ispartofseries | 72; | |
dc.rights | Y | en |
dc.subject | Older adults | en |
dc.subject | Middle age | en |
dc.subject | Cystatin C | en |
dc.subject | Chronic kidney disease | en |
dc.title | 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 | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/mlittle | |
dc.identifier.peoplefinderurl | http://people.tcd.ie/rkenny | |
dc.identifier.rssinternalid | 182639 | |
dc.rights.ecaccessrights | openAccess | |
dc.identifier.orcid_id | 0000-0001-6003-397X | |
dc.identifier.uri | https://jech.bmj.com/content/72/4/287 | |
dc.identifier.uri | http://hdl.handle.net/2262/91774 | |