Division of Nephrology and Hypertension, Department of Medicine, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY, USA.
Department of Transplantation Medicine, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY, USA.
Clin Transplant. 2021 Feb;35(2):e14200. doi: 10.1111/ctr.14200. Epub 2021 Jan 21.
Identifying kidney transplant recipients at risk for graft failure following BK virus nephropathy (BKVN) may allow personalization of therapy. We have reported that a noninvasive composite signature of urinary cell level of plasminogen activator inhibitor-1(PAI-1) mRNA and serum creatinine level, measured at the time of BKVN diagnosis, is prognostic of graft failure. In this investigation, we determined whether the composite signature is prognostic of graft failure in an independent cohort of 25 patients with BKVN. Of the 25 patients, 8 developed graft failure and 17 did not. We measured urinary cell levels of PAI-1 mRNA, 18S rRNA, and BKV VP1 mRNA at the time of BKVN diagnosis and evaluated clinical parameters including Banff pathology scores, acute rejection, and graft function. The area under the receiver operating characteristic curve for the noninvasive composite signature was 0.95 (P < .001) for prognosticating graft failure. The previously reported threshold of -0.858 predicted graft failure with a sensitivity of 75% and a specificity of 94%. Our current study validates the use of composite signature and the threshold of -0.858 to identify those at risk for graft failure following BKVN diagnosis, and supports future studies utilizing the composite signature score to personalize treatment of BKVN.
确定 BK 病毒肾病 (BKVN) 后发生移植物衰竭的肾移植受者,可能有助于实现治疗的个体化。我们曾报道,在 BKVN 诊断时测量的尿细胞纤溶酶原激活物抑制剂-1(PAI-1)mRNA 水平和血清肌酐水平的无创复合标志物可预测移植物衰竭。在本研究中,我们在 25 例 BKVN 患者的独立队列中确定了该复合标志物是否可预测移植物衰竭。在这 25 例患者中,8 例发生移植物衰竭,17 例未发生。我们在 BKVN 诊断时测量了尿细胞 PAI-1 mRNA、18S rRNA 和 BKV VP1 mRNA 的水平,并评估了包括 Banff 病理评分、急性排斥反应和移植物功能在内的临床参数。无创复合标志物预测移植物衰竭的受试者工作特征曲线下面积为 0.95(P<.001)。以前报道的阈值-0.858 预测移植物衰竭的灵敏度为 75%,特异性为 94%。我们的研究验证了复合标志物和阈值-0.858 用于识别 BKVN 诊断后发生移植物衰竭风险的应用,并支持未来利用复合标志物评分来实现 BKVN 个体化治疗的研究。