肾移植受者发生BK多瘤病毒的危险因素及治疗结果:一项8年回顾性队列研究

IF 1.9
Alyssa Pradhan, Melanie Wyld, Susan Wan, Rebecca Davis, Kushani Jayasinghe, Kate Wyburn
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引用次数: 0

摘要

背景:bkpyv - dna血症发生在高达30%的肾移植受者(KTRs)中,并伴有移植物威胁性bkpyv肾病的发生率高达10%。bkpyv - dna血症、bkpyv肾病和相关移植物丢失的危险因素描述不完整。我们试图确定bkpyv - dna血症的患病率、危险因素和长期影响。方法:对2010 - 2018年成人ktr进行单中心回顾性研究。我们使用逻辑回归来确定bkpyv - dna血症的优势比(OR),并使用生存分析来评估bkpyv - dna血症对移植物和患者生存的影响。结果:522例患者中,100例(19%)发生bkpyv - dna血症,43例(8.2%)发生bkpyv肾病,导致2个移植物丢失。与bkpyv - dna血症相关的因素为非高加索人种(OR 1.76, CI 0.98-3.16)、移植前糖尿病(OR 2.06, CI 1.02-4.14)、HLA错配3/6或4/6 (OR 2.37, CI 1.06-5.56)和HLA错配5/6和6/6 (OR 2.53, CI 1.20-5.63)。此外,急性移植和移植后第一个月急性排斥反应后每天大于25mg的泼尼松龙剂量与bkpyv - dna血症的风险增加相关(OR分别为3.06,CI 1.66-6.06和OR 2.36, CI 1.16-4.75)。在10年的随访中,bkpyv - dna血症和bkpyv肾病的发展与移植物减少或患者生存无关。结论:虽然bkpyv - dna血症和bkpyv肾病在KTR中仍然普遍存在,但相关的移植物丢失率很低,对移植物或患者的长期生存没有明显的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk Factors for the Development of BK Polyomavirus and Treatment Outcomes in Kidney Transplant Recipients: An 8-Year Retrospective Cohort Study.

Background: BKPyV-DNAemia occurs in up to 30% of kidney transplant recipients (KTRs), with graft-threatening BKPyV-nephropathy in up to 10%. Risk factors for BKPyV-DNAemia, BKPyV-nephropathy, and associated graft loss are incompletely described. We sought to determine the prevalence, risk factors for, and long-term impact of BKPyV-DNAemia.

Methods: A single-centre retrospective study of adult KTRs between 2010 and 2018. We used logistic regression to determine odds ratios (OR) of BKPyV-DNAemia, and survival analysis to assess the impact of BKPyV-DNAemia on graft and patient survival.

Results: Of 522 patients, 100 (19%) developed BKPyV-DNAemia and 43 (8.2%) developed BKPyV-nephropathy, resulting in the loss of two grafts. Factors associated with the development of BKPyV-DNAemia were non-Caucasian ethnicity (OR 1.76, CI 0.98-3.16), pre-transplant diabetes (OR 2.06, CI 1.02-4.14) and HLA mismatch of 3/6 or 4/6 (OR 2.37, CI 1.06-5.56) and HLA mismatch of 5/6 and 6/6 (OR 2.53, CI 1.20-5.63). Additionally, a greater than 25 mg per day prednisolone dose following acute transplant and acute rejection in the first month post-transplant was associated with an increased risk of BKPyV-DNAemia (OR 3.06, CI 1.66-6.06 and OR 2.36, CI 1.16-4.75 respectively). Over a 10-year follow-up, the development of BKPyV-DNAemia and BKPyV-nephropathy was not associated with reduced graft or patient survival.

Conclusion: While BKPyV-DNAemia and BKPyV-nephropathy remain prevalent in KTR, there were low rates of associated graft loss and no demonstrable impact on long-term graft or patient survival.

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