Long-Term Outcomes after Acute Rejection in Kidney Transplant Recipients: An ANZDATA Analysis

被引:101
作者
Clayton, Philip A. [1 ,2 ,3 ]
McDonald, Stephen P. [1 ,2 ,3 ]
Russ, Graeme R. [1 ,2 ,3 ]
Chadban, Steven J. [1 ,4 ,5 ]
机构
[1] SAHMRI, Australia & New Zealand Dialysis & Transplant ANZ, Adelaide, SA, Australia
[2] Univ Adelaide, Adelaide Med Sch, Adelaide, SA, Australia
[3] Royal Adelaide Hosp, Cent & Northern Adelaide Renal & Transplantat Ser, Adelaide, SA, Australia
[4] Royal Prince Alfred Hosp, Dept Renal Med, Sydney, NSW, Australia
[5] Univ Sydney, Charles Perkins Ctr, Kidney Node, Sydney, NSW, Australia
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2019年 / 30卷 / 09期
基金
英国医学研究理事会;
关键词
ANTIBODY-MEDIATED REJECTION; RISK-FACTOR; ALLOGRAFT SURVIVAL; NEW-ZEALAND; IMPACT; CYCLOSPORINE; AUSTRALIA; CANCER;
D O I
10.1681/ASN.2018111101
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Declining rates of acute rejection (AR) and the high rate of 1-year graft survival among patients with AR have prompted re-examination of AR as an outcome in the clinic and in trials. Yet AR and its treatment may directly or indirectly affect longer-term outcomes for kidney transplant recipients. Methods To understand the long-term effect of AR on outcomes, we analyzed data from the Australia and New Zealand Dialysis and Transplant Registry, including 13,614 recipients of a primary kidney-only transplant between 1997 and 2017 with at least 6 months of graft function. The associations between AR within 6 months post-transplant and subsequent cause-specific graft loss and death were determined using Cox models adjusted for baseline donor, recipient, and transplant characteristics. Results AR occurred in 2906 recipients (21.4%) and was associated with graft loss attributed to chronic allograft nephropathy (hazard ratio [HR], 1.39; 95% confidence interval [95% CI], 1.23 to 1.56) and recurrent AR beyond month 6 (HR, 1.85; 95% CI, 1.39 to 2.46). Early AR was also associated with death with a functioning graft (HR, 1.22; 95% CI, 1.08 to 1.36), and with death due to cardiovascular disease (HR, 1.30; 95% CI, 1.11 to 1.53) and cancer (HR, 1.35; 95% CI, 1.12 to 1.64). Sensitivity analyses restricted to subgroups with either biopsy-proven, antibody-mediated, or vascular rejection, or stratified by treatment response produced similar results. Conclusions AR is associated with increased risks of longer-term graft failure and death, particularly death from cardiovascular disease and cancer. The results suggest AR remains an important short-term outcome to monitor in kidney transplantation and clinical trials.
引用
收藏
页码:1697 / 1707
页数:11
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