The use of urinary biomarkers to predict acute kidney injury in children after liver transplant

被引:17
作者
Fuhrman, Dana Y. [1 ,2 ,3 ]
Kellum, John A. [2 ]
Joyce, Emily L. [2 ,3 ]
Miyashita, Yosuke [3 ]
Mazariegos, George V. [4 ]
Ganoza, Armando [4 ]
Squires, James E. [5 ]
机构
[1] Univ Pittsburgh, Childrens Hosp Pittsburgh, Med Ctr, Dept Crit Care Med, Pittsburgh, PA 15213 USA
[2] Ctr Crit Care Nephrol, Dept Crit Care Med, Pittsburgh, PA USA
[3] Univ Pittsburgh, Childrens Hosp Pittsburgh, Dept Pediat, Div Pediat Nephrol,Med Ctr, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Childrens Hosp Pittsburgh, Med Ctr, Hillman Ctr Pediat Liver Transplantat, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Childrens Hosp Pittsburgh, Med Ctr, Div Pediat Gastroenterol Hepatol & Nutr, Pittsburgh, PA 15213 USA
关键词
kidney disease; liver transplantation; pediatrics; tubular biomarkers; GELATINASE-ASSOCIATED LIPOCALIN; DISEASE; HYPERFILTRATION; DEFINITION; VALIDATION; CREATININE; MARKER; RISK;
D O I
10.1111/petr.13608
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background AKI after pediatric liver transplantation is associated with increased morbidity and mortality. The role of urinary biomarkers for the prediction of AKI in pediatric patients after liver transplantation has not been previously reported. The primary objective of this prospective pilot study was to determine the predictive capabilities of urinary KIM-1, NGAL, TIMP-2, and IGFBP7 for diagnosing AKI. Methods Sixteen children undergoing liver transplantation were enrolled in the study over a 19-month time period. The Kidney Disease Improving Outcomes criteria for urine output and serum creatinine were used to define AKI. Predictive ability was evaluated using the area under the curve obtained by ROC analysis. Results AKI occurred in 6 (37.5%) of the patients between 2 and 4 days after transplant. There were no differences in any of the biomarkers prior to transplant. When obtained within 6 hours after transplant, the area under the ROC curve for predicting AKI was 0.758 (95% CI: 0.458-1.00) for KIM-1, 0.900 (95% CI: 0.724-1.00) for NGAL, and 0.933 (95% CI: 0.812-1.00) for the product of TIMP-2 and IGFBP7 ([TIMP-2]center dot[IGFBP7]). Conclusions Our results show that both NGAL and [TIMP-2]center dot[IGFBP7] provide significant discrimination for AKI risk following liver transplant in children. Larger studies are needed to determine the optimal time point for measuring these biomarkers and to validate our findings.
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页数:6
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