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Published on: September 11, 2020
Urinary biomarkers of AKI and mortality 3 years after cardiac surgery
Steven G Coca1, Amit X Garg2, Heather Thiessen-Philbrook2
1Section of Nephrology, Yale University School of Medicine, Program of Applied Translational Research, Veterans Affairs Connecticut Healthcare System, New Haven, Connecticut;
Insights
Urinary biomarkers like IL-18 and KIM-1 after surgery can predict long-term mortality risk in patients with or without acute kidney injury (AKI). These kidney injury biomarkers offer valuable prognostic insights for patient outcomes.
Area of Science:
- Nephrology
- Cardiovascular Surgery
- Biomarker Research
Background:
- Urinary biomarkers for acute kidney injury (AKI) are known to predict in-hospital outcomes.
- Limited data exists on their association with long-term mortality post-surgery.
- Prognostic value of kidney injury biomarkers for long-term mortality remains under-explored.
Purpose of the Study:
- To assess the association between urinary kidney injury biomarkers and all-cause mortality.
- To evaluate prognostic value in patients undergoing cardiac surgery with long-term follow-up.
- To determine if biomarkers predict mortality in both clinical AKI and non-AKI patients.
Main Methods:
- International, multicenter, prospective cohort study of 1199 adult cardiac surgery patients.
- Measurement of five urinary biomarkers (neutrophil gelatinase-associated lipocalin, IL-18, KIM-1, liver fatty acid binding protein, albumin) on postoperative days 1-3.
- Median follow-up of 3.0 years, assessing all-cause mortality.
Main Results:
- Among patients with clinical AKI, highest tertiles of all five biomarkers independently associated with 2.0- to 3.2-fold increased mortality risk.
- In patients without clinical AKI, highest tertiles of IL-18 and KIM-1 independently associated with long-term mortality.
- IL-18 and KIM-1 showed significant net reclassification improvements for predicting 3-year mortality in non-AKI patients.
Conclusions:
- Urinary kidney injury biomarkers, especially IL-18 and KIM-1, offer significant prognostic information.
- These biomarkers predict 3-year mortality risk in both patients with and without clinical AKI post-cardiac surgery.
- Postoperative urinary biomarker assessment can enhance long-term mortality risk stratification.
Abstract:
Urinary biomarkers of AKI provide prognostic value for in-hospital outcomes, but little is known about their association with longer-term mortality after surgery. We sought to assess the association between kidney injury biomarkers and all-cause mortality in an international, multicenter, prospective long-term follow-up study from six clinical centers in the United States and Canada composed of 1199 adults who underwent cardiac surgery between 2007 and 2009 and were enrolled in the Translational Research in Biomarker Endpoints in AKI cohort. On postoperative days 1-3, we measured the following five urinary biomarkers: neutrophil gelatinase-associated lipocalin, IL-18, kidney injury molecule-1 (KIM-1), liver fatty acid binding protein, and albumin. During a median follow-up of 3.0 years (interquartile range, 2.2-3.6 years), 139 participants died (55 deaths per 1000 person-years). Among patients with clinical AKI, the highest tertiles of peak urinary neutrophil gelatinase-associated lipocalin, IL-18, KIM-1, liver fatty acid binding protein, and albumin associated independently with a 2.0- to 3.2-fold increased risk for mortality compared with the lowest tertiles. In patients without clinical AKI, the highest tertiles of peak IL-18 and KIM-1 also associated independently with long-term mortality (adjusted hazard ratios [95% confidence intervals] of 1.2 [1.0 to 1.5] and 1.8 [1.4 to 2.3] for IL-18 and KIM-1, respectively), and yielded continuous net reclassification improvements of 0.26 and 0.37, respectively, for the prediction of 3-year mortality. In conclusion, urinary biomarkers of kidney injury, particularly IL-18 and KIM-1, in the immediate postoperative period provide additional prognostic information for 3-year mortality risk in patients with and without clinical AKI.
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