Tubular Injury and Cell-Cycle Arrest Biomarkers To Predict Acute Kidney Injury in Noncritically Ill Children Receiving Aminoglycosides

Hayton Chui(Hospital for Sick Children), Jillian S. Caldwell(Montreal Children's Hospital), Mariya Yordanova(Montreal Children's Hospital), Vedran Cockovski(Hospital for Sick Children), Daniel Fredric(Hospital for Sick Children), Maya Harel‐Sterling(Montreal Children's Hospital), Maya Haasz(University of Toronto), Zubaida Al‐Ismaili(Montreal Children's Hospital), Michael Pizzi(Montreal Children's Hospital), Qing Ma(Cincinnati Children's Hospital Medical Center), Prasad Devarajan(Cincinnati Children's Hospital Medical Center), Stuart L. Goldstein(Cincinnati Children's Hospital Medical Center), Michael Zappitelli(Hospital for Sick Children)
Biomarkers in Medicine
July 1, 2020
Cited by 14Open Access
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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.


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