4.6 Article

Performance of Serum Creatinine and Kidney Injury Biomarkers for Diagnosing Histologic Acute Tubular Injury

Journal

AMERICAN JOURNAL OF KIDNEY DISEASES
Volume 70, Issue 6, Pages 807-816

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.ajkd.2017.06.031

Keywords

Acute kidney injury (AKI); acute tubular injury (ATI); serum creatinine (Scr); NGAL; L-FABP; KIM-1; IL-18; kidney biopsy; kidney histology; subclinical AKI; kidney injury biomarker; diagnostic performance

Funding

  1. National Institutes of Health (NIH) [RO1DK-93770, K24DK090203]
  2. Roche Organ Transplantation Research Foundation Award
  3. American Heart Association
  4. National Institute of Diabetes and Digestive and Kidney Diseases [K23-097201]
  5. Yale Kidney O'Brien Center Award [P30DK79337]
  6. Health Resources and Services Administration [234-2005-37011C]
  7. T32 training grant from NIH [T32DK007276]
  8. Robert E. Leet and Clara Guthrie Patterson Trust Mentored Clinical Research Award
  9. Clinical and Translational Science Award from the National Center for Advancing Translational Science, a component of the NIH [UL1 TR000142]

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Background: The diagnosis of acute kidney injury (AKI), which is currently defined as an increase in serum creatinine (Scr) concentration, provides little information on the condition's actual cause. To improve phenotyping of AKI, many urinary biomarkers of tubular injury are being investigated. Because AKI cases are not frequently biopsied, the diagnostic accuracy of concentrations of Scr and urinary biomarkers for histologic acute tubular injury is unknown. Study Design: Cross-sectional analysis from multicenter prospective cohort. Settings & Participants: Hospitalized deceased kidney donors on whom kidney biopsies were performed at the time of organ procurement for histologic evaluation. Predictors: (1) AKI diagnosed by change in Scr concentration during donor hospitalization and (2) concentrations of urinary biomarkers (neutrophil gelatinase-associated lipocalin [NGAL], liver-type fatty acid-binding protein [L-FABP], interleukin 18 [IL-18], and kidney injury molecule 1 [KIM-1]) measured at organ procurement. Outcome: Histologic acute tubular injury. Results: Of 581 donors, 98 (17%) had mild acute tubular injury and 57 (10%) had severe acute tubular injury. Overall, Scr-based AKI had poor diagnostic performance for identifying histologic acute tubular injury and 49% of donors with severe acute tubular injury did not have AKI. The area under the receiver operating characteristic curve (AUROC) of change in Scr concentration for diagnosing severe acute tubular injury was 0.58 (95% CI, 0.49-0.67) and for any acute tubular injury was 0.52 (95% CI, 0.45-0.58). Compared with Scr concentration, NGAL concentration demonstrated higher AUROC for diagnosing both severe acute tubular injury (0.67; 95% CI, 0.60-0.74; P = 0.03) and any acute tubular injury (0.60; 95% CI, 0.55-0.66; P 5 0.005). In donors who did not have Scr-based AKI, NGAL concentrations were higher with increasing severities of acute tubular injury (subclinical AKI). However, compared with Scr concentration, AUROCs for acute tubular injury diagnosis were not significantly higher for urinary L-FABP, IL-18, or KIM-1. Limitations: The spectrum of AKI cause in deceased donors may be different from that of a general hospitalized population. Conclusions: Concentrations of Scr and kidney injury biomarkers (L-FABP, IL-18, and KIM-1) lack accuracy for diagnosing acute tubular injury in hospitalized deceased donors. Although urinary NGAL concentration had slightly higher discrimination for acute tubular injury than did Scr concentration, its overall AUROC was still modest. Published by Elsevier Inc. on behalf of the National Kidney Foundation, Inc. This is a US Government Work. There are no restrictions on its use.

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