AI Article Synopsis

  • The study investigates the effectiveness of kidney biomarkers in predicting major adverse kidney events (MAKE) in critically ill patients with acute kidney injury (AKI) and compares these predictions to traditional serum creatinine levels.
  • Blood and urine samples were collected from AKI patients and matched controls to evaluate the association of biomarkers like NGAL and cystatin C with MAKE at hospital discharge.
  • Findings indicate that higher levels of NGAL and cystatin C correlate significantly with increased risk of MAKE-DC, suggesting these biomarkers could enhance clinical prediction models for kidney-related complications.*

Article Abstract

Background: Several biomarkers of AKI have been examined for their ability to predict AKI before serum creatinine. Few studies have focused on using kidney biomarkers to better predict major adverse kidney events (MAKE), an increasingly used composite outcome in critical care nephrology research.

Methods: Single-center prospective study collecting blood and urine samples from critically ill patients with AKI Kidney Disease Improving Global Outcomes stage 2 or above, and matched controls from a single, tertiary care intensive care unit (ICU). Samples were collected at 24-48 hours after AKI diagnosis (patients) or ICU admission (controls), 5-7 days later, and 4-6 weeks after discharge for patients with AKI. The primary outcome of interest was MAKE at hospital discharge (MAKE-DC), consisting of the composite end point of death, RRT dependence, or a decrease in estimated glomerular filtration to <75% of baseline.

Results: Serum/urinary neutrophil gelatinase-associated lipocalin (NGAL), serum/urinary cystatin C, and urinary kidney injury molecule-1 early in the AKI or ICU course were all significantly higher in patients with MAKE-DC compared with those not experiencing MAKE-DC. Additionally, serum/urinary NGAL and serum cystatin C measurements at the first time point remained significantly associated with MAKE events at 3, 6, and 12 months. Serum cystatin C, and to a lesser extent serum NGAL, significantly improved upon a logistic regression clinical prediction model of MAKE-DC (AUROC 0.94 and 0.87 versus 0.83; =0.001 and =0.02, respectively). Patients without MAKE-DC experienced a greater decline in serum NGAL from first to second measurement than those patients experiencing MAKE-DC.

Conclusions: Early measures of kidney biomarkers in patients who are critically ill are associated with MAKE-DC. This relationship appears to be greatest with serum NGAL and cystatin C, which display additive utility to a clinical prediction model. Trending serum NGAL may also have utility in predicting MAKE-DC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785730PMC
http://dx.doi.org/10.34067/KID.0003552020DOI Listing

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