Diagnostic value of urinary kidney injury molecule 1 for acute kidney injury: a meta-analysis

PLoS One. 2014 Jan 3;9(1):e84131. doi: 10.1371/journal.pone.0084131. eCollection 2014.

Abstract

Background: Urinary Kidney Injury Molecule 1 (KIM-1) is a proximal tubular injury biomarker for early detection of acute kidney injury (AKI), with variable performance characteristics depending on clinical and population settings.

Methods: Meta-analysis was performed to assess the diagnostic value of urinary KIM-1 in AKI. Relevant studies were searched from MEDLINE, EMBASE, Pubmed, Elsevier Science Direct, Scopus, Web of Science, Google Scholar and Cochrane Library. Meta-analysis methods were used to pool sensitivity and specificity and to construct summary receiver operating characteristic (SROC) curves.

Results: A total of 2979 patients from 11 eligible studies were enrolled in the analysis. Five prospective cohorts, two cross-sectional and four case-control studies were identified for meta-analysis. The estimated sensitivity of urinary KIM-1 for the diagnosis of AKI was 74.0% (95% CI, 61.0%-84.0%), and specificity was 86.0% (95% CI, 74.0%-93.0%). The SROC analysis showed an area under the curve of 0.86(0.83-0.89). Subgroup analysis suggested that population settings and detection time were the key factors affecting the efficiency of KIM-1 for AKI diagnosis.

Limitation: Various population settings, different definition of AKI and Serum creatinine level used as the standard might have influence on AKI diagnosis. The relatively small number of studies and heterogeneity between them also affected the evaluation.

Conclusion: Urinary KIM-1 may be a promising biomarker for early detection of AKI with considerable predictive value, especially for cardiac surgery patients, and its potential value needs to be validated in large studies and across a broader scope of clinical settings.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / diagnosis*
  • Acute Kidney Injury / urine*
  • Biomarkers / urine
  • Hepatitis A Virus Cellular Receptor 1
  • Humans
  • Membrane Glycoproteins / urine*
  • Odds Ratio
  • Prognosis
  • Publication Bias
  • Receptors, Virus
  • Sensitivity and Specificity

Substances

  • Biomarkers
  • HAVCR1 protein, human
  • Hepatitis A Virus Cellular Receptor 1
  • Membrane Glycoproteins
  • Receptors, Virus

Grants and funding

This study was supported in part by the National Basic Research Program of China 973 Program No. 2012CB517600 (No. 2012CB517602). The study was also sponsored by the National Natural Science Foundation of China (81102700 and 81373865), National “Twelfth Five-Year” Plan for Science & Technology Support No. 2011BAI10B00 and by grants 10JC1410100, 12401906400 and 13401906100 from the Science and Technology Commission of Shanghai Municipality, China. Program ZXSNXD-CC-ZDYJ002 from the Shanghai Health Bureau and Funding scheme for training young teachers in Colleges and Universities in Shanghai were also included. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.