Biomarkers of acute kidney injury

被引:503
作者
Vaidya, Vishal S. [1 ]
Ferguson, Michael A. [2 ]
Bonventre, Joseph V. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Renal, Boston, MA 02115 USA
[2] Childrens Hosp, Div Nephrol, Boston, MA 02115 USA
关键词
acute renal failure; clusterin; cystatin-C; cysteine-rich protein-61 (CYR-61); ELISA; interleukin-18 (IL-18); kidney injury molecule-1 (Kim-1); microfluidics; nanotechnology; neutrophil gelatinase-associated lipocalin (NGAL);
D O I
10.1146/annurev.pharmtox.48.113006.094615
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Acute kidney injury (AKI) is a common condition with a high risk of death. The standard metrics used to define and monitor the progression of AKI, such as serum creatinine and blood urea nitrogen levels, are insensitive, nonspecific, and change significantly only after significant kidney injury and then with a substantial time delay. This delay in diagnosis not only prevents timely patient management decisions, including administration of putative therapeutic agents, but also significantly affects the preclinical evaluation of toxicity thereby allowing potentially nephrotoxic drug candidates to pass the preclinical safety criteria only to be found to be clinically nephrotoxic with great human costs. Studies to establish effective therapies for AKI will be greatly facilitated by two factors: (a) development of sensitive, specific, and reliable biomarkers for early diagnosis/prognosis of AKI in preclinical and clinical studies, and (b) development and validation of high-throughput innovative technologies that allow rapid multiplexed detection of multiple markers at the bedside.
引用
收藏
页码:463 / 493
页数:31
相关论文
共 140 条
  • [41] THE SGP-2 GENE IS DEVELOPMENTALLY REGULATED IN THE MOUSE KIDNEY AND ABNORMALLY EXPRESSED IN COLLECTING DUCT CYSTS IN POLYCYSTIC KIDNEY-DISEASE
    HARDING, MA
    CHADWICK, LJ
    GATTONE, VH
    CALVET, JP
    [J]. DEVELOPMENTAL BIOLOGY, 1991, 146 (02) : 483 - 490
  • [42] Hart Susan G. Emeigh, 2005, Journal of Pharmacological and Toxicological Methods, V52, P30
  • [43] Prognostic value of tubular proteinuria and enzymuria in nonoliguric acute tubular necrosis
    Herget-Rosenthal, S
    Poppen, D
    Hüsing, J
    Marggraf, G
    Pietruck, F
    Jakob, HG
    Philipp, T
    Kribben, A
    [J]. CLINICAL CHEMISTRY, 2004, 50 (03) : 552 - 558
  • [44] Herget-Rosenthal S, 2005, CLIN NEPHROL, V64, P41
  • [45] Elevation of CXCR3-binding chemokines in urine indicates acute renal-allograft dysfunction
    Hu, HZ
    Aizenstein, BD
    Puchalski, A
    Burmania, JA
    Hamawy, MM
    Knechtle, SJ
    [J]. AMERICAN JOURNAL OF TRANSPLANTATION, 2004, 4 (03) : 432 - 437
  • [46] Hudkins KL, 1999, J AM SOC NEPHROL, V10, P444
  • [47] Osteopontin expression in human crescentic glomerulonephritis
    Hudkins, KL
    Giachelli, CM
    Eitner, F
    Couser, WG
    Johnson, RJ
    Alpers, CE
    [J]. KIDNEY INTERNATIONAL, 2000, 57 (01) : 105 - 116
  • [48] The contribution of adult stem cells to renal repair
    Humphreys, Benjamin D.
    Bonventre, Joseph V.
    [J]. NEPHROLOGIE & THERAPEUTIQUE, 2007, 3 (01): : 3 - 10
  • [49] Mesenchymal stem cells in acute kidney injury
    Humphreys, Benjamin D.
    Bonventre, Joseph V.
    [J]. ANNUAL REVIEW OF MEDICINE, 2008, 59 : 311 - 325
  • [50] 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
    Ichimura, T
    Bonventre, JV
    Bailly, V
    Wei, H
    Hession, CA
    Cate, RL
    Sanicola, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (07) : 4135 - 4142