Tubular injury and cell-cycle arrest biomarkers to predict acute kidney injury in noncritically ill children receiving aminoglycosides

Biomark Med. 2020 Jul;14(10):879-894. doi: 10.2217/bmm-2019-0419. Epub 2020 Aug 18.

Abstract

Aim: NGAL, IL-18, KIM-1 as well as urinary TIMP2 and IGFBP7 and their mathematical product (TIMP2*IGFBP7) were evaluated for detecting pediatric aminoglycoside acute kidney injury (AG-AKI). Methods: In a prospective study, noncritically ill children received aminoglycosides (AG) ≥3 days. The area under the curve (AUC) for biomarkers to detect AKI was calculated by a) days before AKI onset; b) treatment days. Results: There were 113 AG episodes (68% febrile neutropenia). The AKI group had a higher proportion with febrile neutropenia. The AKI group had significantly lower NGAL 3 days before AKI, as patients with febrile neutropenia had a lower NGAL during AG treatment (p < 0.05). NGAL, IL-18 and TIMP2*IGFBP7 had AUC ≥0.73 at 3, 2 and 2 days before AKI onset. Conclusion: NGAL, IL-18 and TIMP2*IGFBP7 were modest early biomarkers of AG-AKI. Febrile neutropenia was associated with lower NGAL.

Keywords: acute kidney injury; aminoglycosides; cell-cycle arrest biomarker; children; noncritically ill; tubular injury biomarker.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / diagnosis
  • Acute Kidney Injury / metabolism*
  • Acute Kidney Injury / pathology*
  • Aminoglycosides / pharmacology*
  • Biomarkers / metabolism
  • Cell Cycle Checkpoints* / drug effects
  • Child
  • Female
  • Humans
  • Kidney Tubules / drug effects
  • Kidney Tubules / injuries*
  • Male
  • Prognosis

Substances

  • Aminoglycosides
  • Biomarkers