ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Abstract: FR-PO1143

Phenotypes of Donor eGFR Trajectories in Living Donor Kidney Transplantation: A Nationwide Prospective Cohort Study

Session Information

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.