Urine NGAL and IL-18 are predictive biomarkers for delayed graft function following kidney transplantation

被引:411
作者
Parikh, C. R.
Jani, A.
Mishra, J.
Ma, Q.
Kelly, C.
Barasch, J.
Edelstein, C. L.
Devarajan, P. [1 ]
机构
[1] Univ Cincinnati, Childrens Hosp, Med Ctr, Cincinnati, OH 45221 USA
[2] Yale Univ, New Haven, CT USA
[3] Univ Colorado, Denver, CO 80202 USA
[4] Columbia Univ, New York, NY 10027 USA
关键词
acute kidney injury; biomarkers; delayed graft function; interleukin-18;
D O I
10.1111/j.1600-6143.2006.01352.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Delayed graft function (DGF) due to tubule cell injury frequently complicates deceased donor kidney transplants. We tested whether urinary neutrophil gelatinase-associated lipocalin (NGAL) and interleukin-18 (IL-18) represent early biomarkers for DGF (defined as dialysis requirement within the first week after transplantation). Urine samples collected on day 0 from recipients of living donor kidneys (n = 23), deceased donor kidneys with prompt graft function (n = 20) and deceased donor kidneys with DGF (n = 10) were analyzed in a double blind fashion by ELISA for NGAL and IL-18. In patients with DGF, peak postoperative serum creatinine requiring dialysis typically occurred 2-4 days after transplant. Urine NGAL and IL-18 values were significantly different in the three groups on day 0, with maximally elevated levels noted in the DGF group (p < 0.0001). The receiver-operating characteristic curve for prediction of DGF based on urine NGAL or IL-18 at day 0 showed an area under the curve of 0.9 for both biomarkers. By multivariate analysis, both urine NGAL and IL-18 on day 0 predicted the trend in serum creatinine in the posttransplant period after adjusting for effects of age, gender, race, urine output and cold ischemia time (p < 0.01). Our results indicate that urine NGAL and IL-18 represent early, predictive biomarkers of DGF.
引用
收藏
页码:1639 / 1645
页数:7
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