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非胰岛素依赖型糖尿病显性肾病的进展

Progression of overt nephropathy in non-insulin-dependent diabetes.

作者信息

Myers B D, Nelson R G, Tan M, Beck G J, Bennett P H, Knowler W C, Blouch K, Mitch W E

机构信息

Division of Nephrology, Stanford University School of Medicine, California, USA.

出版信息

Kidney Int. 1995 Jun;47(6):1781-9. doi: 10.1038/ki.1995.246.

DOI:10.1038/ki.1995.246
PMID:7543961
Abstract

The detection of overt albuminuria (> 300 mg/g creatinine) in the absence of azotemia was used to diagnose early nephropathy in 34 Pima Indians with NIDDM of 16 +/- 1 years duration. Differential solute clearances were performed serially to define the course of the glomerular injury over 48 months. At baseline, the GFR (107 +/- 5 ml/min), filtration fraction and sieving coefficients of relatively permeant dextrans (< 52 A) were all depressed below corresponding values in 20 normoalbuminuric Pima Indians with a similar duration of NIDDM. Over the ensuing 48 months the GFR (-34%) and filtration fraction (-13%) in the nephropathic patients declined further. The sieving coefficients of large, nearly impermeant dextrans (> 56 A radius) increased selectively and fractional clearances of albumin and IgG increased correspondingly by > 10-fold. Analysis of the findings with pore theory revealed: (1) a progressive decline in pore density and the ultrafiltration coefficient (Kf); and (2) broadening of glomerular pore-size distribution that resulted in greater prominence of large pores (> 70 A radius). We conclude that increasing loss of intrinsic ultrafiltration capacity is the predominant cause of the early and progressive decline in GFR that follows the development of nephropathy in NIDDM. We speculate that progressive impairment of barrier size-selectivity contributes to but does not fully account for the increasingly heavy proteinuria that is observed early in the course of this disorder.

摘要

在34名病程为16±1年的皮马族印第安2型糖尿病患者中,在无氮质血症的情况下检测到显性白蛋白尿(>300mg/g肌酐)用于诊断早期肾病。连续进行不同溶质清除率测定以确定48个月内肾小球损伤的进程。基线时,与20名病程相似的正常白蛋白尿皮马族印第安人相比,肾病患者的肾小球滤过率(GFR,107±5ml/min)、滤过分数以及相对通透的右旋糖酐(<52A)的筛系数均低于相应值。在随后的48个月里,肾病患者的GFR(-34%)和滤过分数(-13%)进一步下降。大的、几乎不通透的右旋糖酐(半径>56A)的筛系数选择性增加,白蛋白和IgG的分数清除率相应增加>10倍。用孔理论分析这些结果显示:(1)孔密度和超滤系数(Kf)逐渐下降;(2)肾小球孔径分布变宽,导致大孔(半径>70A)更加突出。我们得出结论,内在超滤能力的丧失增加是2型糖尿病肾病发生后GFR早期和进行性下降的主要原因。我们推测屏障大小选择性的进行性损害促成了但不能完全解释在该疾病病程早期观察到的越来越严重的蛋白尿。

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