Gramlick Madelyn E, Trevillian Paul, Palazzi Kerrin L, Heer Munish K
Surgical Services, John Hunter Hospital, Hunter New England Local Health District, Newcastle, NSW, Australia.
Newcastle Transplant Unit, Division of Surgery, John Hunter Hospital, Hunter New England Local Health District, Newcastle, NSW, Australia.
Transplant Direct. 2022 Feb 21;8(3):e1295. doi: 10.1097/TXD.0000000000001295. eCollection 2022 Mar.
HLA matching has been the cornerstone of deceased donor kidney allocation policies worldwide but can lead to racial inequity. Although HLA matching has been shown to improve clinical outcomes, the long-term impacts of nonallogenic factors are being increasingly recognized. This has led some transplant programs to include points for nonallogenic factors, for example, age. Our study looks at long-term graft and patient outcomes based on allocation cohorts rather than individual number of HLA mismatches.
Using the Australia and New Zealand Dialysis and Transplant Registry, we analyzed 7440 adult deceased donor transplant events from 2000 to 2018. Transplants were classified as HLA matched or nonmatched according to the OrganMatch score and the local allocation algorithms. Graft function was studied with linear mixed modeling and graft rejection with logistic and binomial regression. Time to graft failure and recipient survival were examined with Kaplan-Meier curve and Cox regression models.
Forty percent of transplants were HLA matched. Mean glomerular filtration rate was 1.76 mL/min/1.73 m higher in the matched transplants ( < 0.001). Matched transplants had longer time to graft failure (15.9 versus 12.7 y; < 0.001) and improved recipient survival (risk of death hazard ratio, 0.83; = 0.003). Matched recipients spent less time on dialysis (28.1 versus 44.8 mo; < 0.001), and this significantly contributed to the benefits seen in graft loss and recipient survival. Caucasian recipients were more likely to receive a matched transplant than non-Caucasians.
Matched transplants showed benefits in graft and recipient outcomes; however, some of these results were of small magnitude, whereas others seemed to be due in part to a reduction in time on dialysis. The benefit for the matched cohort came at the expense of the nonmatched cohort, who spent longer on dialysis and were more likely to be of a minority racial background.
人类白细胞抗原(HLA)匹配一直是全球尸体供肾分配政策的基石,但可能导致种族不平等。尽管HLA匹配已被证明可改善临床结局,但非同种异体因素的长期影响正日益受到认可。这使得一些移植项目将非同种异体因素纳入评分,例如年龄。我们的研究基于分配队列而非个体HLA错配数量来观察长期移植物和患者结局。
利用澳大利亚和新西兰透析与移植登记处的数据,我们分析了2000年至2018年期间7440例成人尸体供肾移植事件。根据器官匹配评分和当地分配算法,将移植分为HLA匹配或不匹配。采用线性混合模型研究移植物功能,采用逻辑回归和二项回归研究移植排斥反应。用Kaplan-Meier曲线和Cox回归模型检查移植物失功时间和受者生存率。
40%的移植为HLA匹配。匹配移植的平均肾小球滤过率高1.76 mL/min/1.73 m(<0.001)。匹配移植的移植物失功时间更长(15.9年对12.7年;<0.001),受者生存率提高(死亡风险比,0.83;=0.003)。匹配的受者透析时间更短(28.1个月对44.8个月;<0.001),这显著促成了在移植物丢失和受者生存方面所见的益处。白人受者比非白人受者更有可能接受匹配的移植。
匹配移植在移植物和受者结局方面显示出益处;然而,其中一些结果幅度较小,而其他一些似乎部分归因于透析时间的减少。匹配队列的益处是以不匹配队列的利益为代价的,不匹配队列透析时间更长,且更可能属于少数种族背景。