ISSN 1006-298X      CN 32-1425/R

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肾脏病与透析肾移植杂志 ›› 2016, Vol. 25 ›› Issue (6): 501-506.DOI: 10.3969/cndt.j.issn.1006-298X.2016.06.001

• 论文 •    下一篇


尿液microRNA-196a与肾脏疾病患者远期预后的关系

  

  • 出版日期:2016-12-28 发布日期:2017-01-03

Urinary microRNA-196a as a predictor of longterm outcome in patients with kidney disease

  • Online:2016-12-28 Published:2017-01-03

摘要:

目的:探讨尿液microRNA196a(miR196a)能否作为预测局灶节段性肾小球硬化(FSGS)远期预后的生物标志物。
方法:收集FSGS患者和正常对照的尿液和血浆标本,分析尿液和血浆miR196a水平与FSGS活动性的关系。入选231例经肾活检确诊的FSGS,qRTPCR方法检测尿液miR196a水平,评估尿液miR196a对FSGS预后的预测价值。
结果:尿液miR196a水平在活动性FSGS患者组显著高于肾脏疾病完全缓解组和正常对照组(P<0001),血浆miR196a水平在三组之间无明显差异,表明尿液miR196a是一种主要来源于肾脏的生物标志物。231例随访患者中,43例进展为终末期肾病(ESRD)。发生ESRD的患者尿液miR196a水平显著高于未发生ESRD的患者(P=0025)。尿液miR196a水平与蛋白尿和估算的肾小球滤过率(eGFR)相关,与肾间质纤维化评分存在相关性。随着尿液miR196a水平增加,患者发生ESRD的风险增加。校正年龄、性别、蛋白尿、eGFR后尿液miR196a升高仍是患者进展至ESRD的独立危险因素。
结论:尿液miR196a是FSGS患者发生ESRD的独立危险因素,可能成为预测FSGS远期预后的新型生物标志物。

Abstract:

Objective: To investigate the association between urinary microRNA196a (miR196a) and longterm outcome in patients with focal segmental glomerulosclerosis(FSGS).
Methodology:Urinary and plasma miR196a were tested in patients with active FSGS(FSGSA), FSGS in complete remission(FSGSCR) and normal controls(NC) 231 FSGS patients were then enrolled at the time of renal biopsy and urinary miR196a levels were measured by qRTPCR. The relationship between urinary miR196a and longterm outcome of FSGS was analyzed.
Results:Urinary miR196a levels were significantly increased in FSGSA patients as compared with FSGSCR patients and NCs(P<0001). However, plasma miR196a levels showed no difference among the three groups, suggesting that the change of urinary miR196a was mainly kidney derived. Of the 231 patients, 43 patients developed endstage renal disease(ESRD) during the followup period. Urinary miR196a levels were significantly higher in patients who progressed to ESRD than those not progressed to ESRD(P=0025). Urinary miR196a was associated with proteinuria, eGFR, and interstitial fibrosis. Patients with higher urinary miR196a levels had a higher cumulative incidence of ESRD. Risk persisted after adjusting for age, sex, proteinuria, and eGFR.
Conclusion:Urinary miR196a is an independent risk factor of ESRD, facilitating early identification of those who will subsequently develop ESRD.