Center For Primary Care and Prevention, Memorial Hospital of Rhode Island, Pawtucket, Rhode Island, USA.
Klinikum rechts der Isar, Technische Universität, München, Germany.
Am J Nephrol. 2018;47(4):275-282. doi: 10.1159/000489095. Epub 2018 Apr 26.
Uromodulin is a kidney-derived glycoprotein and putative tubular function index. Lower serum uromodulin was recently associated with increased risk for kidney allograft failure in a preliminary, longitudinal single-center -European study involving 91 kidney transplant recipients (KTRs).
The Folic Acid for Vascular Outcome Reduction in Transplantation (FAVORIT) trial is a completed, large, multiethnic controlled clinical trial cohort, which studied chronic, stable KTRs. We conducted a case cohort analysis using a randomly selected subset of patients (random subcohort, n = 433), and all individuals who developed kidney allograft failure (cases, n = 226) during follow-up. Serum uromodulin was determined in this total of n = 613 FAVORIT trial participants at randomization. Death-censored kidney allograft failure was the study outcome.
The 226 kidney allograft failures occurred during a median surveillance of 3.2 years. Unadjusted, weighted Cox proportional hazards modeling revealed that lower serum uromodulin, tertile 1 vs. tertile 3, was associated with a threefold greater risk for kidney allograft failure (hazards ratio [HR], 95% CI 3.20 [2.05-5.01]). This association was attenuated but persisted at twofold greater risk for allograft failure, after adjustment for age, sex, smoking, allograft type and vintage, prevalent diabetes mellitus and cardiovascular disease (CVD), total/high-density lipoprotein cholesterol ratio, systolic blood pressure, estimated glomerular filtration rate, and natural log urinary albumin/creatinine: HR 2.00, 95% CI (1.06-3.77).
Lower serum uromodulin, a possible indicator of less well-preserved renal tubular function, remained associated with greater risk for kidney allograft failure, after adjustment for major, established clinical kidney allograft failure and CVD risk factors, in a large, multiethnic cohort of long-term, stable KTRs.
尿调蛋白是一种肾脏来源的糖蛋白,也是一种潜在的肾小管功能指标。最近,在一项涉及 91 名肾移植受者(KTR)的初步、纵向单中心-欧洲研究中,较低的血清尿调蛋白与肾移植失败风险增加相关。
叶酸用于减少移植中的血管结局(FAVORIT)试验是一项已完成的、大型的、多民族对照临床试验队列,研究了慢性、稳定的 KTR。我们使用一个随机选择的患者子集(随机亚组,n = 433)进行病例队列分析,所有在随访期间发生肾移植失败(病例,n = 226)的个体。在总共 n = 613 名 FAVORIT 试验参与者中,在随机分组时测定了血清尿调蛋白。以死亡为终点的肾移植失败是研究结局。
226 例肾移植失败发生在中位监测 3.2 年期间。未经调整的、加权 Cox 比例风险模型显示,较低的血清尿调蛋白,第 1 三分位与第 3 三分位相比,与肾移植失败的三倍风险相关(风险比[HR],95%置信区间[CI] 3.20[2.05-5.01])。在调整年龄、性别、吸烟、移植类型和使用年限、现患糖尿病和心血管疾病(CVD)、总/高密度脂蛋白胆固醇比值、收缩压、估计肾小球滤过率和尿白蛋白/肌酐自然对数后,这种关联虽然减弱但仍存在,移植失败的风险增加两倍:HR 2.00,95%CI(1.06-3.77)。
在一个大型的、多民族的长期稳定的 KTR 队列中,较低的血清尿调蛋白,一种可能表明肾小管功能保存较差的指标,在调整主要的、已确定的临床肾移植失败和 CVD 风险因素后,与肾移植失败的风险增加相关。