Abstract: FR-PO1143
Phenotypes of Donor eGFR Trajectories in Living Donor Kidney Transplantation: A Nationwide Prospective Cohort Study
Session Information
- Transplantation: Clinical - Transplant Access, Recipient Evaluation, Living Donors, Pregnancy, and More
October 23, 2026 | Location: Exhibit Hall A, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Transplantation
- 2002 Transplantation: Clinical
Authors
- Lee, Yu ho, Kyung Hee University, Dongdaemun-gu, Seoul, Korea (the Republic of)
- Lee, Jeong-Yeun, Kyung Hee University, Dongdaemun-gu, Seoul, Korea (the Republic of)
- Yoon, Soo-Young, Kyung Hee University, Dongdaemun-gu, Seoul, Korea (the Republic of)
- Kim, Jinsug, Kyung Hee University, Dongdaemun-gu, Seoul, Korea (the Republic of)
- Jeong, Kyunghwan, Kyung Hee University, Dongdaemun-gu, Seoul, Korea (the Republic of)
- Hwang, Hyeon Seok, Kyung Hee University, Dongdaemun-gu, Seoul, Korea (the Republic of)
Background
Post-donation kidney function varies considerably among living kidney donors. However, longitudinal patterns of estimated glomerular filtration rate (eGFR) after nephrectomy and their clinical implications remain incompletely characterized.
Methods
We analyzed data from 5,510 living kidney donors and their matched recipients enrolled in a nationwide prospective cohort. Longitudinal post-donation eGFR measurements were used to identify donor trajectory classes. Donor characteristics and matched recipient graft outcomes were evaluated across donor eGFR trajectory phenotypes.
Results
Four distinct donor eGFR trajectory classes were identified: class 1 (stable, 84.2%), class 2 (higher initial values followed by mild decline and recovery, 10.8%), class 3 (gradual and sustained increase, 3.9%), and class 4 (rapid early increase followed by a rapid decline, 1.1%). Younger donor age and higher baseline eGFR were independently associated with class 4 compared with class 1. Class 4 donors showed higher cumulative incidence of post-donation kidney dysfunction, including ≥50% eGFR decline and eGFR <45 ml/min/1.73 m. Recipients of class 4 donors had higher risks of death-censored and all-cause graft loss than those of class 1 donors (adjusted hazard ratio [95% confidence interval] of 2.63 [1.14–6.06], and 3.30 [1.72–6.34], respectively).
Conclusion
Living kidney donors exhibit heterogeneous eGFR trajectories after nephrectomy. A high-risk trajectory with a rapid early increase followed by a rapid decline was associated with adverse post-donation kidney outcomes of the donors and a higher risk of graft loss in matched recipients.