Urinary biomarkers in the early diagnosis of acute kidney injury

被引:428
作者
Han, W. K. [1 ]
Waikar, S. S. [1 ]
Johnson, A. [1 ]
Betensky, R. A. [2 ]
Dent, C. L. [3 ]
Devarajan, P. [4 ]
Bonventre, J. V. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[3] Univ Cincinnati, Coll Med, Cincinnati Childrens Hosp, Med Ctr,Dept Cardiol, Cincinnati, OH USA
[4] Univ Cincinnati, Coll Med, Cincinnati Childrens Hosp, Med Ctr,Dept Nephrol & Hypertens, Cincinnati, OH USA
关键词
acute kidney injury; MMP-9; NAG; KIM-1;
D O I
10.1038/sj.ki.5002715
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
A change in the serum creatinine is not sensitive for an early diagnosis of acute kidney injury. We evaluated urinary levels of matrix metalloproteinase-9 (MMP-9), N-acetyl-beta-D-glucosaminidase (NAG), and kidney injury molecule-1 (KIM-1) as biomarkers for the detection of acute kidney injury. Urine samples were collected from 44 patients with various acute and chronic kidney diseases, and from 30 normal subjects in a cross-sectional study. A case-control study of children undergoing cardio-pulmonary bypass surgery included urine specimens from each of 20 patients without and with acute kidney injury. Injury was defined as a greater than 50% increase in the serum creatinine within the first 48h after surgery. The biomarkers were normalized to the urinary creatinine concentration at 12, 24, and 36 h after surgery with the areas under the receiver-operating characteristic curve compared for performance. In the cross-sectional study, the area under the curve for MMP-9 was least sensitive followed by KIM-1 and NAG. Combining all three biomarkers achieved a perfect score diagnosing acute kidney injury. In the case-control study, KIM-1 was better than NAG at all time points, but combining both was no better than KIM-1 alone. Urinary MMP-9 was not a sensitive marker in the case-control study. Our results suggest that urinary biomarkers allow diagnosis of acute kidney injury earlier than a rise in serum creatinine.
引用
收藏
页码:863 / 869
页数:7
相关论文
共 23 条
[1]  
American Society of Nephrology, 2005, J Am Soc Nephrol, V16, P1886
[2]   Angiostatin and matrix metalloprotease expression following ischemic acute renal failure [J].
Basile, DP ;
Fredrich, K ;
Weihrauch, D ;
Hattan, N ;
Chilian, WM .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 286 (05) :F893-F902
[3]   PREDICTIVE VALUE OF URINARY N-ACETYL-BETA-D-GLUCOSAMINIDASE (NAG), ALANINE-AMINOPEPTIDASE (AAP) AND BETA-2-MICROGLOBULIN (BETA-2M) IN EVALUATING NEPHROTOXICITY OF GENTAMICIN [J].
GIBEY, R ;
DUPOND, JL ;
ALBER, D ;
DESFLORIS, RL ;
HENRY, JC .
CLINICA CHIMICA ACTA, 1981, 116 (01) :25-34
[4]   Kidney Injury Molecule-1 (KIM-1): A novel biomarker for human renal proximal tubule injury [J].
Han, WK ;
Bailly, V ;
Abichandani, R ;
Thadhani, R ;
Bonventre, JV .
KIDNEY INTERNATIONAL, 2002, 62 (01) :237-244
[5]   Human kidney injury molecule-1 is a tissue and urinary tumor marker of renal cell carcinoma [J].
Han, WK ;
Alinani, A ;
Wu, CL ;
Michaelson, D ;
Loda, M ;
McGovern, FJ ;
Thadhani, R ;
Bonventre, JV .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (04) :1126-1134
[6]  
Han Won K, 2004, Curr Opin Crit Care, V10, P476, DOI 10.1097/01.ccx.0000145095.90327.f2
[7]   A METHOD OF COMPARING THE AREAS UNDER RECEIVER OPERATING CHARACTERISTIC CURVES DERIVED FROM THE SAME CASES [J].
HANLEY, JA ;
MCNEIL, BJ .
RADIOLOGY, 1983, 148 (03) :839-843
[8]   HOSPITAL-ACQUIRED RENAL-INSUFFICIENCY - A PROSPECTIVE-STUDY [J].
HOU, SH ;
BUSHINSKY, DA ;
WISH, JB ;
COHEN, JJ ;
HARRINGTON, JT .
AMERICAN JOURNAL OF MEDICINE, 1983, 74 (02) :243-248
[9]   Kidney injury molecule-1: a tissue and urinary biomarker for nephrotoxicant-induced renal injury [J].
Ichimura, T ;
Hung, CC ;
Yang, SA ;
Stevens, JL ;
Bonventre, JV .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 286 (03) :F552-F563
[10]   Kidney injury molecule-1 (KIM-1), a putative epithelial cell adhesion molecule containing a novel immunoglobulin domain, is up-regulated in renal cells after injury [J].
Ichimura, T ;
Bonventre, JV ;
Bailly, V ;
Wei, H ;
Hession, CA ;
Cate, RL ;
Sanicola, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (07) :4135-4142