pISSN 3022-6783
eISSN 3022-7712

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Korean J Transplant 2022; 36(Suppl 1): S4-S4

Published online November 17, 2022

https://doi.org/10.4285/ATW2022.F-0681

© The Korean Society for Transplantation

Transition of metabolic dysfunction after kidney transplantation and its association with transplant outcomes: a nationwide prospective cohort study

Yu Ho Lee1, Sang Heon Song2, Seung Hwan Song3, Ho Sik Shin4, Jaeseok Yang5, Myoung Soo Kim6, Hyeon Seok Hwang7

1Department of Nephrology, Bundang CHA General Hospital, Seongnam, Korea
2Department of Nephrology, Pusan National University, Busan, Korea
3Department of Surgery, Ewha Womans University, Seoul, Korea
4Department of Nephrology, Kosin University, Busan, Korea
5Department of Nephrology, Yonsei University, Seoul, Korea
6Department of Surgery, Yonsei University, Seoul, Korea
7Department of Nephrology, Kyung Hee University, Seoul, Korea

Correspondence to: Hyeon Seok Hwang
E-mail: hwanghsne@gmail.com

Abstract

Background: Kidney transplantation is expected to modify the metabolic status. However, it remains unclear whether the transition of metabolic status before and after transplantation affects the transplant outcomes.
Methods: We analyzed 4,187 kidney transplant recipients registered in a nationwide prospective cohort from 2014 to 2020. Metabolic dysfunction (MD) was considered, if three conditions are met (body mass index, blood pressure, fasting blood glucose, triglyceride, and high-density lipoprotein cholesterol level). Patients were categorized into four groups based on the presence of MD at pretransplant and 1-year posttransplant. The primary outcome was the occurrence of death-censored graft failure and patient death.
Results: Prevalence of pre- and posttransplant MD was 49.0% and 40.1%, respectively. Among recipients without pretransplant MD, 19.6% developed MD at 1-year posttransplantation. By contrast, MD disappeared in 38.7% of the recipients with pretransplant MD. The cumulative event rate of composite of graft failure and patient death was significantly higher in both recipients with newly developed posttransplant MD and recipients with persistent MD (P<0.001). Compared to recipients without pre- and posttransplant MD, those with newly developed posttransplant MD showed an increased risk of graft failure (adjusted hazard ratio [HR], 2.50; 95% confidence interval [CI], 1.74–3.58) and those with persistent MD had higher risk of patient death (adjusted HR, 3.21; 95% CI, 1.40–7.39). The risk of composite event was increased as more metabolic components was converted to be dysfunctional after transplantation. An analysis of each component of MD showed that a normalization of blood pressure after transplantation led to a decrease in the risk of composite event.
Conclusions: Kidney transplantation significantly affects the metabolic status in patients with end-stage kidney disease. Newly developed posttransplant MD increases the risk of graft loss and persistent posttransplant MD adversely affects patient survival, suggesting that transition of metabolic status was significantly associated with kidney transplant outcomes.