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优化监测小儿肾移植受者同种异体移植炎症的方法:连续尿 CXCL10/肌酐检测。

Optimizing the approach to monitoring allograft inflammation using serial urinary CXCL10/creatinine testing in pediatric kidney transplant recipients.

机构信息

University of British Columbia, Vancouver, British Columbia, Canada.

BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.

出版信息

Pediatr Transplant. 2024 May;28(3):e14718. doi: 10.1111/petr.14718.

Abstract

BACKGROUND

Urinary CXCL10/creatinine (uCXCL10/Cr) is proposed as an effective biomarker of subclinical rejection in pediatric kidney transplant recipients. This study objective was to model implementation in the clinical setting.

METHODS

Banked urine samples at a single center were tested for uCXCL10/Cr to validate published thresholds for rejection diagnosis (>80% specificity). The positive predictive value (PPV) for rejection diagnosis for uCXCL10/Cr-indicated biopsy was modeled with first-positive versus two-test-positive approaches, with accounting for changes associated with urinary tract infection (UTI), BK and CMV viremia, and subsequent recovery.

RESULTS

Seventy patients aged 10.5 ± 5.6 years at transplant (60% male) had n = 726 urine samples with n = 236 associated biopsies (no rejection = 167, borderline = 51, and Banff 1A = 18). A threshold of 12 ng/mmol was validated for Banff 1A versus no-rejection diagnosis (AUC = 0.74, 95% CI = 0.57-0.92). The first-positive test approach (n = 69) did not resolve a clinical diagnosis in 38 cases (55%), whereas the two-test approach resolved a clinical diagnosis in the majority as BK (n = 17/60, 28%), CMV (n = 4/60, 7%), UTI (n = 8/60, 13%), clinical rejection (n = 5/60, 8%), and transient elevation (n = 18, 30%). In those without a resolved clinical diagnosis, PPV from biopsy for subclinical rejection is 24% and 71% (p = .017), for first-test versus two-test models, respectively. After rejection treatment, uCXCL10/Cr level changes were all concordant with change in it-score. Sustained uCXCL10/Cr after CMV and BK viremia resolution was associated with later acute rejection.

CONCLUSIONS

Urinary CXCL10/Cr reliably identifies kidney allograft inflammation. These data support a two-test approach to reliably exclude other clinically identifiable sources of inflammation, for kidney biopsy indication to rule out subclinical rejection.

摘要

背景

尿 CXCL10/肌酐(uCXCL10/Cr)被提议作为小儿肾移植受者亚临床排斥反应的有效生物标志物。本研究的目的是建立临床模型。

方法

在单个中心的储存尿液样本中检测 uCXCL10/Cr,以验证发表的排斥诊断阈值(特异性>80%)。使用首次阳性与两次阳性测试方法,结合尿路感染(UTI)、BK 和 CMV 病毒血症以及随后的恢复,对 uCXCL10/Cr 指示活检的排斥诊断阳性预测值(PPV)进行建模。

结果

70 名 10.5±5.6 岁的患者(60%为男性)在移植时接受了 n=726 份尿液样本和 n=236 份相关活检(无排斥反应 n=167、边缘型 n=51、Banff 1A n=18)。12ng/mmol 的阈值可用于 Banff 1A 与无排斥反应诊断(AUC=0.74,95%CI=0.57-0.92)。首次阳性测试方法(n=69)在 38 例(55%)中无法明确临床诊断,而两次测试方法可在大多数情况下明确临床诊断,如 BK(n=17/60,28%)、CMV(n=4/60,7%)、UTI(n=8/60,13%)、临床排斥反应(n=5/60,8%)和一过性升高(n=18,30%)。在未明确临床诊断的患者中,活检对亚临床排斥的 PPV 分别为首次检测模型的 24%和两次检测模型的 71%(p=0.017)。接受排斥治疗后,uCXCL10/Cr 水平的变化与 it 评分的变化完全一致。CMV 和 BK 病毒血症消退后,uCXCL10/Cr 持续升高与迟发性急性排斥反应相关。

结论

尿 CXCL10/Cr 可靠地识别肾脏移植物炎症。这些数据支持采用两次检测方法来可靠排除其他可识别的炎症源,以便进行肾脏活检以排除亚临床排斥反应。

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