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

被引:409
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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共 30 条
  • [1] Defining acute renal failure: physiological principles
    Bellomo, R
    Kellum, JA
    Ronco, C
    [J]. INTENSIVE CARE MEDICINE, 2004, 30 (01) : 33 - 37
  • [2] Delayed graft function influences renal function, but not survival
    Boom, H
    Mallat, MJK
    De Fijter, JW
    Zwinderman, AH
    Paul, LC
    [J]. KIDNEY INTERNATIONAL, 2000, 58 (02) : 859 - 866
  • [3] Prediction of delayed renal allograft function using an artificial neural network
    Brier, ME
    Ray, PC
    Klein, JB
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2003, 18 (12) : 2655 - 2659
  • [4] Cellular and molecular derangements in acute tubular necrosis
    Devarajan, P
    [J]. CURRENT OPINION IN PEDIATRICS, 2005, 17 (02) : 193 - 199
  • [5] Gene expression in early ischemic renal injury: clues towards pathogenesis, biomarker discovery, and novel therapeutics
    Devarajan, P
    Mishra, J
    Supavekin, S
    Patterson, LT
    Potter, SS
    [J]. MOLECULAR GENETICS AND METABOLISM, 2003, 80 (04) : 365 - 376
  • [6] Delayed graft function of more than six days strongly decreases long-term survival of transplanted kidneys
    Giral-Classe, M
    Hourmant, M
    Cantarovich, D
    Dantal, J
    Blancho, G
    Daguin, P
    Ancelet, D
    Soulillou, JP
    [J]. KIDNEY INTERNATIONAL, 1998, 54 (03) : 972 - 978
  • [7] AJT 2001: the Genesis
    Halloran, PF
    [J]. AMERICAN JOURNAL OF TRANSPLANTATION, 2001, 1 (01) : 1 - 3
  • [8] Discovery of protein biomarkers for renal diseases
    Hewitt, SM
    Dear, J
    Star, RA
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (07): : 1677 - 1689
  • [9] Nomogram for predicting the likelihood of delayed graft function in adult cadaveric renal transplant recipients
    Irish, WD
    Mccollum, DA
    Tesi, RJ
    Owen, AB
    Brennan, DC
    Bailly, JE
    Schnitzler, MA
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (11): : 2967 - 2974
  • [10] Laparoscopic donor nephrectomy: The University of Maryland 6-year experience
    Jacobs, SC
    Cho, E
    Foster, C
    Liao, P
    Bartlett, ST
    [J]. JOURNAL OF UROLOGY, 2004, 171 (01) : 47 - 51