Comprehensive Transplant Center, Department of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Agence de la Biomedecine, Paris, France.
Am J Transplant. 2023 Jan;23(1):45-54. doi: 10.1016/j.ajt.2022.08.001. Epub 2023 Jan 11.
The demand for donors' kidneys continues to increase amid a shortage of available donors. Managing policies to thoughtfully allocate this scarce resource is a complex process. Although human leukocyte antigen (HLA) matching has been shown to prolong graft survival, its relative contribution to allocation schemes is empirically compromised owing to competing priorities. We explored using a new metric, Matched Donor Potential (MDP), to facilitate improved HLA matching while promoting equity. We interrogated all active kidney waitlist patients (N = 164 427), their corresponding unacceptable antigen files, and all effective donors in the Scientific Registry of Transplant Recipients (January 1, 2016-December 31, 2017). Cause-specific hazard functions were evaluated to assess the potential impact of the MDP metric on deceased donor transplant access rates for all candidates. Access was affected by ethnicity, blood group type, and calculated Panel Reactive Antibody (cPRA). Importantly, we show that access to transplantation is influenced by the patient's own HLA makeup regardless of their ethnicity and by the HLA makeup of effective donors. The MDP metric demonstrates a high association with access to transplantation. Adjusting Cox models to include this new metric resulted in improved access to kidney transplantation for waitlist candidates of minority heritage while significantly promoting HLA matching. Thus, the MDP metric accounts for balanced, equitable organ allocation algorithms.
在可供器官短缺的情况下,对供体肾脏的需求持续增加。管理政策以深思熟虑的方式分配这种稀缺资源是一个复杂的过程。尽管人类白细胞抗原 (HLA) 匹配已被证明可以延长移植物的存活期,但由于存在竞争优先级,其对分配方案的相对贡献在经验上受到损害。我们探索使用一种新的衡量标准,即匹配供体潜力 (MDP),以促进 HLA 匹配的改进,同时促进公平。我们调查了所有活跃的肾脏候补名单患者(N = 164427)、他们对应的不可接受的抗原文件以及科学移植受者登记处(2016 年 1 月 1 日至 2017 年 12 月 31 日)中的所有有效供体。评估了特定原因的危险函数,以评估 MDP 衡量标准对所有候选人的已故供体移植准入率的潜在影响。准入受种族、血型和计算的 Panel Reactive Antibody (cPRA) 影响。重要的是,我们表明,无论患者的种族如何,以及有效供体的 HLA 构成如何,移植的准入都受到患者自身 HLA 构成的影响。MDP 衡量标准与移植准入高度相关。调整 Cox 模型以包含此新衡量标准可显著提高少数族裔候补名单候选人的肾脏移植准入率,同时显著促进 HLA 匹配。因此,MDP 衡量标准考虑了平衡、公平的器官分配算法。