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BK 病毒相关性肾病:中性粒细胞明胶酶相关脂质运载蛋白作为一种新的诊断工具?

BK virus-associated nephropathy: neutrophil gelatinase-associated lipocalin as a new diagnostic tool?

机构信息

Medizinische Klinik und Poliklinik IV, Nephrologisches Zentrum, Klinikum der Universität München, Ludwig-Maximilians-University, Munich, Germany.

出版信息

Clin Transplant. 2013 Mar-Apr;27(2):E184-91. doi: 10.1111/ctr.12081. Epub 2013 Feb 13.

Abstract

INTRODUCTION

BK nephropathy has emerged as an important cause for allograft failure in renal transplant patients. The kidney tubules are the main target of BK virus infiltration. Neutrophil gelatinase-associated lipocalin (NGAL) has been proven to be a powerful biomarker for tubular damage. Therefore, we investigated the suitability of plasma NGAL as new diagnostic tool in patients with BK infection.

MATERIAL AND METHODS

We retrospectively analyzed 240 renal transplant recipients. Systematic BKV screening by plasma PCR was performed one month after transplantation and every three month thereafter for two yr. Plasma NGAL concentration was investigated using a commercial ELISA. Medical records and electronic databases were reviewed for clinical parameters.

RESULTS

BK viremia (BKV+) was diagnosed in 5.0% (12/240) and BK nephropathy in 3.3% (8/240) of our patients. BKV+ patients received more induction therapy (p = 0.03) and experienced a higher rate of biopsy-proven rejections compared to 13 control patients with similar graft function but negative BKV PCR. Contrary to our hypothesis, there was no difference in plasma NGAL expression between both groups (128.6 vs. 172.2 ng/mL; p = 0.68).

CONCLUSIONS

Intensified immunosuppressive therapy is associated with an increased risk for BK nephropathy. Plasma NGAL is neither suitable for diagnosing BK nephropathy nor helpful in predicting the individual course of patients with BKV infection.

摘要

简介

BK 肾病已成为肾移植患者移植肾功能丧失的重要原因。肾脏小管是 BK 病毒浸润的主要靶标。中性粒细胞明胶酶相关脂质运载蛋白(NGAL)已被证明是肾小管损伤的有力生物标志物。因此,我们研究了血浆 NGAL 作为 BK 感染患者新的诊断工具的适用性。

材料与方法

我们回顾性分析了 240 例肾移植受者。移植后 1 个月和此后每 3 个月进行一次血浆 PCR 系统性 BKV 筛查,持续 2 年。使用商业 ELISA 检测血浆 NGAL 浓度。回顾性分析病历和电子数据库中的临床参数。

结果

我们患者中有 5.0%(12/240)诊断为 BK 病毒血症(BKV+),3.3%(8/240)诊断为 BK 肾病。与 13 例具有相似移植物功能但 BKV PCR 阴性的对照患者相比,BKV+患者接受更多的诱导治疗(p=0.03),且活检证实排斥反应的发生率更高。与我们的假设相反,两组之间的血浆 NGAL 表达无差异(128.6 vs. 172.2ng/ml;p=0.68)。

结论

强化免疫抑制治疗与 BK 肾病的风险增加有关。血浆 NGAL 既不适合诊断 BK 肾病,也无助于预测 BKV 感染患者的个体病程。

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