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Updated: Feb 2, 2026

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Published on: August 14, 2019
Donor Urinary C5a Levels Independently Correlate With Posttransplant Delayed Graft Function
Bernd Schröppel1,2, Peter S Heeger2, Heather Thiessen-Philbrook3
1Section of Nephrology, University Hospital, Ulm, Germany.
Background:
Accumulating evidence implicates the complement cascade as pathogenically contributing to ischemia-reperfusion injury and delayed graft function (DGF) in human kidney transplant recipients. Building on observations that kidney injury can initiate in the donor before nephrectomy, we tested the hypothesis that anaphylatoxins C3a and C5a in donor urine before transplantation associate with risk of posttransplant injury.
Methods:
We evaluated the effects of C3a and C5a in donor urine on outcomes of 469 deceased donors and their corresponding 902 kidney recipients in a subset of a prospective cohort study.
Results:
We found a threefold increase of urinary C5a concentrations in donors with stage 2 and 3 acute kidney injury (AKI) compared donors without AKI (P < 0.001). Donor C5a was higher for the recipients with DGF (defined as dialysis in the first week posttransplant) compared with non-DGF (P = 0.002). In adjusted analyses, C5a remained independently associated with recipient DGF for donors without AKI (relative risk, 1.31; 95% confidence interval, 1.13-1.54). For donors with AKI, however, urinary C5a was not associated with DGF. We observed a trend toward better 12-month allograft function for kidneys from donors with C5a concentrations in the lowest tertile (P = 0.09). Urinary C3a was not associated with donor AKI, recipient DGF, or 12-month allograft function.
Conclusions:
Urinary C5a correlates with the degree of donor AKI. In the absence of clinical donor AKI, donor urinary C5a concentrations associate with recipient DGF, providing a foundation for testing interventions aimed at preventing DGF within this high-risk patient subgroup.
Insights
Donor urinary C5a levels predict kidney transplant recipients
Area of Science:
- Nephrology
- Immunology
- Transplantation Immunology
Background:
- The complement cascade contributes to ischemia-reperfusion injury and delayed graft function (DGF) in kidney transplant recipients.
- Kidney injury may begin in the donor before organ procurement.
- Anaphylatoxins C3a and C5a are key complement components implicated in injury.
Purpose of the Study:
- To investigate the association between donor urinary C5a and C3a levels and posttransplant outcomes.
- To determine if donor urine anaphylatoxins predict acute kidney injury (AKI) and DGF in recipients.
Main Methods:
- Evaluated C5a and C3a in donor urine from 469 deceased donors and 902 kidney recipients.
- Correlated urinary C5a/C3a with donor AKI and recipient DGF (dialysis within the first week).
- Performed adjusted analyses to assess independent associations with DGF and graft function.
Main Results:
- Urinary C5a was threefold higher in donors with stage 2-3 AKI.
- Higher donor urinary C5a associated with recipient DGF (P=0.002).
- Donor urinary C5a independently predicted DGF in recipients from donors without AKI (RR 1.31).
- Urinary C3a showed no association with donor AKI or recipient DGF.
- A trend suggested better 12-month allograft function with lower donor C5a tertiles (P=0.09).
Conclusions:
- Urinary C5a concentration correlates with donor kidney injury severity.
- Donor urinary C5a predicts recipient DGF, especially in the absence of clinical donor AKI.
- Donor urinary C5a may identify high-risk transplant scenarios for targeted interventions.
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