Urinary π-glutathione S-transferase Predicts Advanced Acute Kidney Injury Following Cardiovascular Surgery

Kai-Hsiang Shu(Far Eastern Memorial Hospital), Chih‐Hsien Wang(National Taiwan University Hospital), Che‐Hsiung Wu(Taipei Tzu Chi Hospital), Tao‐Min Huang(National Taiwan University Hospital), Pei‐Chen Wu(Mackay Memorial Hospital), Chun‐Fu Lai(National Taiwan University Hospital), Li‐Jung Tseng(National Taiwan University Hospital), Hung‐Bin Tsai(National Taiwan University Hospital), Rory Connolly, Vin‐Cent Wu(National Taiwan University Hospital)
Scientific Reports
August 16, 2016
Cited by 56Open Access
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Abstract

Urinary biomarkers augment the diagnosis of acute kidney injury (AKI), with AKI after cardiovascular surgeries being a prototype of prognosis scenario. Glutathione S-transferases (GST) were evaluated as biomarkers of AKI. Urine samples were collected in 141 cardiovascular surgical patients and analyzed for urinary alpha-(α-) and pi-(π-) GSTs. The outcomes of advanced AKI (KDIGO stage 2, 3) and all-cause in-patient mortality, as composite outcome, were recorded. Areas under the receiver operator characteristic (ROC) curves and multivariate generalized additive model (GAM) were applied to predict outcomes. Thirty-eight (26.9%) patients had AKI, while 12 (8.5%) were with advanced AKI. Urinary π-GST differentiated patients with/without advanced AKI or composite outcome after surgery (p < 0.05 by generalized estimating equation). Urinary π-GST predicted advanced AKI at 3 hrs post-surgery (p = 0.033) and composite outcome (p = 0.009), while the corresponding ROC curve had AUC of 0.784 and 0.783. Using GAM, the cutoff value of 14.7 μg/L for π-GST showed the best performance to predict composite outcome. The addition of π-GST to the SOFA score improved risk stratification (total net reclassification index = 0.47). Thus, urinary π-GST levels predict advanced AKI or hospital mortality after cardiovascular surgery and improve in SOFA outcome assessment specific to AKI.


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