Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12882-017-0629-z
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dc.titleUrinalysis findings and urinary kidney injury biomarker concentrations
dc.contributor.authorNadkarni, G.N
dc.contributor.authorCoca, S.G
dc.contributor.authorMeisner, A
dc.date.accessioned2020-10-27T10:23:53Z
dc.date.available2020-10-27T10:23:53Z
dc.date.issued2017
dc.identifier.citationNadkarni, G.N, Coca, S.G, Meisner, A (2017). Urinalysis findings and urinary kidney injury biomarker concentrations. BMC Nephrology 18 (1) : 218. ScholarBank@NUS Repository. https://doi.org/10.1186/s12882-017-0629-z
dc.identifier.issn14712369
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181265
dc.description.abstractIntroduction: Urinary biomarkers of kidney injury are presumed to reflect renal tubular damage. However, their concentrations may be influenced by other factors, such as hematuria or pyuria. We sought to examine what non-injury related urinalysis factors are associated with urinary biomarker levels. Methods: We examined 714 adults who underwent cardiac surgery in the TRIBE-AKI cohort that did not experience post-operative clinical AKI (patients with serum creatinine change of ? 20% were excluded). We examined the association between urinalysis findings and the pre- and first post-operative urinary concentrations of 4 urinary biomarkers: neutrophil gelatinase-associated lipocalin (NGAL), interleukin-18 (IL-18), kidney injury molecule-1 (KIM-1), and liver fatty acid binding protein (L-FABP). Results: The presence of leukocyte esterase and nitrites on urinalysis was associated with increased urinary NGAL (R2 0.16, p < 0.001 and R2 0.07, p < 0.001, respectively) in pre-operative samples. Hematuria was associated with increased levels of all 4 biomarkers, with a much stronger association seen in post-operative samples (R2 between 0.02 and 0.21). Dipstick proteinuria concentrations correlated with levels of all 4 urinary biomarkers in pre-operative and post-operative samples (R2 between 0.113 and 0.194 in pre-operative and between 0.122 and 0.322 in post-operative samples). Adjusting the AUC of post-operative AKI for dipstick proteinuria lowered the AUC for all 4 biomarkers at the pre-operative time point and for 2 of the 4 biomarkers at the post-operative time point. Conclusions: Several factors available through urine dipstick testing are associated with increased urinary biomarker concentrations that are independent of clinical kidney injury. Future studies should explore the impact of these factors on the prognostic and diagnostic performance of these AKI biomarkers. © 2017 The Author(s).
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectcreatinine
dc.subjectfatty acid binding protein
dc.subjectinterleukin 18
dc.subjectkidney injury molecule 1
dc.subjectliver fatty acid binding protein
dc.subjectneutrophil gelatinase associated lipocalin
dc.subjectnitrite
dc.subjectunclassified drug
dc.subjectbiological marker
dc.subjectacute kidney failure
dc.subjectaged
dc.subjectarea under the curve
dc.subjectArticle
dc.subjectcohort analysis
dc.subjectcreatinine blood level
dc.subjectdisease association
dc.subjectfemale
dc.subjectheart surgery
dc.subjecthematuria
dc.subjecthuman
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectpostoperative period
dc.subjectpreoperative evaluation
dc.subjectproteinuria
dc.subjecturinalysis
dc.subjecturine level
dc.subjectacute kidney failure
dc.subjectclinical trial
dc.subjectinternational cooperation
dc.subjectmiddle aged
dc.subjectmulticenter study
dc.subjectprocedures
dc.subjectprospective study
dc.subjectproteinuria
dc.subjecturine
dc.subjectvery elderly
dc.subjectAcute Kidney Injury
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectBiomarkers
dc.subjectCohort Studies
dc.subjectFemale
dc.subjectHumans
dc.subjectInternationality
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectProspective Studies
dc.subjectProteinuria
dc.subjectUrinalysis
dc.typeArticle
dc.contributor.departmentSURGERY
dc.description.doi10.1186/s12882-017-0629-z
dc.description.sourcetitleBMC Nephrology
dc.description.volume18
dc.description.issue1
dc.description.page218
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