Evaluating the impact of donor eGFR and HLA-DR mismatch on graft survival in living donor kidney transplants.

Frontiers in nephrology Pub Date : 2025-01-07 eCollection Date: 2024-01-01 DOI:10.3389/fneph.2024.1518791
Pooja Budhiraja, Jesse D Schold, Rocio Lopez, Susana Arrigain, Bruce Kaplan
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Abstract

Background: This study assesses the impact of human leukocyte antigen (HLA)-DR mismatch and donor-estimated glomerular filtration rate (eGFR) on outcomes of living donor kidney transplantation (LDKT), which are especially relevant to the availability of multiple donors and paired kidney exchanges.

Methods: Using data from the Scientific Registry of Transplant Recipients (SRTR), we retrospectively analyzed graft survival in adult LDKT recipients transplanted between January 2013 and September 2022. Recipients with 0 HLA-DR mismatches were compared to those with 1-2 HLA-DR mismatches. Cox models assessed the association between donor eGFR and graft and patient survival, stratifying by a) HLA-DR mismatches, and b) HLA-DR mismatches and recipient age.

Results: Among 44,080 recipients, 7,195 had 0 HLA-DR mismatches and 36,885 had 1-2 HLA-DR mismatches. The recipients' mean age was 49.1 for the 0 HLA-DR mismatch group and 50.4 for the 1-2 HLA-DR mismatch group. The donors' mean age was 43.1 and 43.8, with an eGFR of 101.0 and 99.9 ml/min, respectively. A higher donor eGFR was associated with better graft survival. Stratified analyses showed higher donor eGFR levels reduced the risk of graft loss in cases with DR mismatch (p < 0.001) but not in cases without HLA-DR mismatch (p = 0.81). This effect was significant for recipients aged 18-39 and over 60. Similar results were observed for patient survival.

Conclusions: Higher donor eGFR was associated with lower risks of graft loss and patient death in the HLA-DR mismatch group but not the 0 HLA-DR mismatch group. These results emphasize the importance of considering both HLA-DR matching and donor kidney function, particularly for younger recipients to avoid sensitization for future transplants.

评估供体eGFR和HLA-DR错配对活体肾移植移植存活的影响。
背景:本研究评估了人白细胞抗原(HLA)-DR错配和供者估计的肾小球滤过率(eGFR)对活体肾移植(LDKT)结果的影响,这与多个供者和配对肾交换的可用性尤其相关。方法:利用移植受者科学登记处(SRTR)的数据,我们回顾性分析了2013年1月至2022年9月间移植的成年LDKT受者的移植存活率。将0例HLA-DR不匹配的受者与1-2例HLA-DR不匹配的受者进行比较。Cox模型评估了供体eGFR和移植物与患者生存之间的关系,按a) HLA-DR不匹配和b) HLA-DR不匹配和受体年龄进行分层。结果:在44,080名接受者中,7195人有0例HLA-DR不匹配,36,885人有1-2例HLA-DR不匹配。0 HLA-DR不匹配组的平均年龄为49.1岁,1-2 HLA-DR不匹配组的平均年龄为50.4岁。献血者的平均年龄为43.1岁和43.8岁,eGFR分别为101.0和99.9 ml/min。供体eGFR越高,移植物存活率越高。分层分析显示,较高的供体eGFR水平降低了DR不匹配病例的移植物丢失风险(p < 0.001),但在没有HLA-DR不匹配的病例中没有(p = 0.81)。这种效果在18-39岁和60岁以上的接受者中尤为显著。在患者生存方面也观察到类似的结果。结论:在HLA-DR不匹配组中,较高的供体eGFR与较低的移植物丢失和患者死亡风险相关,但与0 HLA-DR不匹配组无关。这些结果强调了考虑HLA-DR匹配和供体肾功能的重要性,特别是对于年轻的受者,以避免未来移植的致敏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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