Biomarkers of AKI: A Review of Mechanistic Relevance and Potential Therapeutic Implications

被引:262
作者
Alge, Joseph L. [1 ]
Arthur, John M. [1 ,2 ]
机构
[1] Med Univ S Carolina, Div Nephrol, Charleston, SC 29425 USA
[2] Ralph H Johnson Vet Affairs Med Ctr, Med Serv, Charleston, SC USA
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2015年 / 10卷 / 01期
基金
美国国家卫生研究院;
关键词
acute renal failure; pathophysiology of renal disease and progression; renin-angiotensin system; ACUTE KIDNEY INJURY; ACID-BINDING PROTEIN; ACUTE-RENAL-FAILURE; GELATINASE-ASSOCIATED LIPOCALIN; ISCHEMIA-REPERFUSION INJURY; EARLY URINARY BIOMARKER; ADULT CARDIAC-SURGERY; INTENSIVE-CARE-UNIT; CHAIN FATTY-ACID; GROWTH-FACTOR-I;
D O I
10.2215/CJN.12191213
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
100201 [内科学]; 100221 [泌尿外科学];
摘要
AKI is a common clinical condition associated with a number of adverse outcomes. More timely diagnosis would allow for earlier intervention and could improve patient outcomes. The goal of early identification of AKI has been the primary impetus for AKI biomarker research, and has led to the discovery of numerous novel biomarkers. However, in addition to facilitating more timely intervention, AKI biomarkers can provide valuable insight into the molecular mechanisms of this complex and heterogeneous disease. Furthermore, AKI biomarkers could also function as molecular phenotyping tools that could be used to direct clinical intervention. This review highlights the major studies that have characterized the diagnostic and prognostic predictive power of these biomarkers. The mechanistic relevance of neutrophil gelatinase-associated lipocalin, kidney injury molecule 1, IL-18, liver-type fatty acid-binding protein, angiotensinogen, tissue inhibitor of metalloproteinase-2, and IGF-binding protein 7 to the pathogenesis and pathobiology of AKI is discussed, putting these biomarkers in the context of the progressive phases of AKI. A biomarker-integrated model of AKI is proposed, which summarizes the current state of knowledge regarding the roles of these biomarkers and the molecular and cellular biology of AKI.
引用
收藏
页码:147 / 155
页数:9
相关论文
共 86 条
[1]
Urinary angiotensinogen predicts adverse outcomes among acute kidney injury patients in the intensive care unit [J].
Alge, Joseph L. ;
Karakala, Nithin ;
Neely, Benjamin A. ;
Janech, Michael G. ;
Velez, Juan Carlos Q. ;
Arthur, John M. .
CRITICAL CARE, 2013, 17 (02)
[2]
Association of Elevated Urinary Concentration of Renin-Angiotensin System Components and Severe AKI [J].
Alge, Joseph L. ;
Karakala, Nithin ;
Neely, Benjamin A. ;
Janech, Michael G. ;
Tumlin, James A. ;
Chawla, Lakhmir S. ;
Shaw, Andrew D. ;
Arthur, John M. .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2013, 8 (12) :2043-2052
[3]
Urinary Angiotensinogen and Risk of Severe AKI [J].
Alge, Joseph L. ;
Karakala, Nithin ;
Neely, Benjamin A. ;
Janech, Michael G. ;
Tomlin, James A. ;
Chawla, Lakhmir S. ;
Shaw, Andrew D. ;
Arthur, John M. .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2013, 8 (02) :184-193
[4]
Differential actions of renal ischemic injury on the intrarenal angiotensin system [J].
Allred, AJ ;
Chappell, MC ;
Ferrario, CM ;
Diz, DI .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 279 (04) :F636-F645
[5]
The Inflammasomes in Kidney Disease [J].
Anders, Hans-Joachim ;
Muruve, Daniel A. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 22 (06) :1007-1018
[6]
Identification of IGFBP-7 by urinary proteomics as a novel prognostic marker in early acute kidney injury [J].
Aregger, Fabienne ;
Uehlinger, Dominik E. ;
Witowski, Janusz ;
Brunisholz, Rene A. ;
Hunziker, Peter ;
Frey, Felix J. ;
Joerres, Achim .
KIDNEY INTERNATIONAL, 2014, 85 (04) :909-919
[7]
Evaluation of 32 urine biomarkers to predict the progression of acute kidney injury after cardiac surgery [J].
Arthur, John M. ;
Hill, Elizabeth G. ;
Alge, Joseph L. ;
Lewis, Evelyn C. ;
Neely, Benjamin A. ;
Janech, Michael G. ;
Tumlin, James A. ;
Chawla, Lakhmir S. ;
Shaw, Andrew D. .
KIDNEY INTERNATIONAL, 2014, 85 (02) :431-438
[8]
Effect of branched-chain fatty acid on lipid dynamics in mice lacking liver fatty acid binding protein gene [J].
Atshaves, BP ;
McIntosh, AL ;
Payne, HR ;
Mackie, J ;
Kier, AB ;
Schroeder, F .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2005, 288 (03) :C543-C558
[9]
Liver fatty acid-binding protein gene ablation inhibits branched-chain fatty acid metabolism in cultured primary hepatocytes [J].
Atshaves, BP ;
McIntosh, AM ;
Lyuksyutova, OI ;
Zipfel, W ;
Webb, WW ;
Schroeder, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (30) :30954-30965
[10]
Evaluation of the incidence and risk factors for development of fenofibrate-associated nephrotoxicity [J].
Attridge, Rebecca L. ;
Linn, William D. ;
Ryan, Laurajo ;
Koeller, Jim ;
Frei, Christopher R. .
JOURNAL OF CLINICAL LIPIDOLOGY, 2012, 6 (01) :19-26