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Urine Complement Factor Ba Identifies Persistent Acute Kidney Injury and Organ Failures in Critically Ill Adults
Erin K Stenson1, Charles E Edelstein2, Zhiying You2
1Department of Pediatrics, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Kidney International Reports
|February 24, 2025
Summary
Elevated urine Ba fragment levels indicate severe acute kidney injury (AKI) and predict poor outcomes. Higher urine Ba is linked to persistent AKI and increased organ failure in critically ill adults.
Area of Science:
- Nephrology
- Critical Care Medicine
- Immunology
Background:
- Critically ill adults with acute kidney injury (AKI) face high mortality and limited treatment options.
- Complement activation is implicated in AKI pathogenesis, but its clinical utility is unclear.
Purpose of the Study:
- To assess the association between complement activation, measured by urine Ba fragment levels, and the development and severity of AKI.
- To determine if urine Ba levels correlate with organ failure outcomes in critically ill patients.
Main Methods:
- Utilized a biorepository of critically ill adults, staging AKI using Kidney Disease Improving Global Outcomes (KDIGO) serum creatinine criteria.
- Measured urine Ba levels via ELISA at ICU admission and 12/24 hours post-admission; analyzed associations with AKI stage, recovery, and organ failure using regression, adjusting for age and APACHE-II score.
Main Results:
- Higher urine Ba levels correlated with increased AKI severity.
- Urine Ba was significantly higher in patients with persistent AKI compared to those with AKI recovery or no AKI.
- Increased urine Ba was associated with worse organ failure outcomes, including fewer ventilator-free, ICU-free, and inotrope-free days.
Conclusions:
- Urine Ba fragment levels are elevated in severe AKI and can differentiate between AKI recovery and persistent AKI.
- A doubling of urine Ba was associated with a 6.6-fold increased odds of persistent AKI.
- Further research is warranted to validate these findings and explore complement inhibition therapies for AKI.
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