Abstract
IntroductionUrinary 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.MethodsWe 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).ResultsThe 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.ConclusionsSeveral 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.
Highlights
Urinary biomarkers of kidney injury are presumed to reflect renal tubular damage
Several studies have shown the efficacy of urinary biomarkers including interleukin-18 (IL-18); plasma neutrophil gelatinase-correlated lipocalin (NGAL); kidney injury molecule-1 (KIM-1) and liver-type fatty acidbinding protein (L-FABP) to detect Acute kidney injury (AKI) before change in serum creatinine. [4–6] These biomarkers have the potential to improve both diagnosis and prognosis of patients with AKI
Since we found proteinuria to have the strongest correlation with the urinary biomarker levels, we examined the impact of adjusting for proteinuria on the diagnostic performance of the biomarkers for stage 2 or 3 AKI in the whole cohort of 1219 participants
Summary
Urinary biomarkers of kidney injury are presumed to reflect renal tubular damage. Their concentrations may be influenced by other factors, such as hematuria or pyuria. We sought to examine what noninjury related urinalysis factors are associated with urinary biomarker levels. [3] For these reasons, Several studies have shown the efficacy of urinary biomarkers including interleukin-18 (IL-18); plasma neutrophil gelatinase-correlated lipocalin (NGAL); kidney injury molecule-1 (KIM-1) and liver-type fatty acidbinding protein (L-FABP) to detect AKI before change in serum creatinine. [4–6] These biomarkers have the potential to improve both diagnosis and prognosis of patients with AKI. Non-injury related factors might impact the association between these biomarkers and AKI. [7] Presence of hematuria and pyuria may potentially affect biomarker concentrations and assay performance in the absence of injury.
Published Version
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