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随着肾单位丢失而改变的蛋白通透性:人类残余肾单位效应的证据。

Changing Protein Permeability with Nephron Loss: Evidence for a Human Remnant Nephron Effect.

机构信息

Newcastle upon Tyne Teaching Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.

Division of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom.

出版信息

Am J Nephrol. 2019;50(2):152-159. doi: 10.1159/000501472. Epub 2019 Jul 3.

Abstract

BACKGROUND

If loss of functioning nephrons predisposes to glomerular barotrauma (a "remnant nephron" effect), then glomerular permeability should increase as glomerular filtration rate (GFR) falls, as is observed in animal models of nephron loss.

METHODS

Changes in net renal protein permeability, defined as proteinuria or albuminuria per mL/min of GFR, were measured in the setting of nephron loss due to kidney donation (Assessing Long Term Outcomes in Living Kidney Donors cohort) or progressive chronic kidney disease (CKD; Modification of Diet in Renal Disease [MDRD], African American Study of Kidney Disease [AASK], and Chronic Renal insufficiency Cohort [CRIC] studies).

RESULTS

Following kidney donation, renal albumin permeability increased by 31% from predonation levels (p < 0.001). With progression of CKD, a 50% loss of residual GFR was accompanied by increases in proteinuria per mL/min GFR of 1.8-, 2.1-, and 1.6-fold in the MDRD, AASK, and CRIC cohorts, respectively (p < 0.001 for all), independent of changes in systolic blood pressure and ACEi/ARB use. A 70% reduction in GFR was associated with permeability increases of 3.1-, 4.4-, and 2.6-fold in the same cohorts. Among MDRD participants with progression of nonglomerular primary disease, the 75th percentile of final permeability was 141 mg/24 h proteinuria per mL/min GFR. This degree of permeability would have resulted in nephrotic range proteinuria had it been present at the baseline mean GFR of 40 mL/min, implying the development of de novo glomerular pathology as GFR fell. Increasing permeability also accompanied CKD progression in participants with nephrotic syndrome at baseline. Consequently, these participants had little improvement in 24 h proteinuria or serum albumin, despite substantial loss of functioning nephron mass across which the protein leak occurred. In the absence of a fall in GFR, there was no increase in permeability in any cohort.

CONCLUSION

Nephron loss is accompanied by an increase in renal protein permeability, even in the absence of a primary glomerular disease. This is consistent with a remnant nephron effect in human CKD.

摘要

背景

如果失去功能的肾单位易导致肾小球过度膨胀(“残余肾单位”效应),那么随着肾小球滤过率(GFR)下降,肾小球通透性应该增加,正如在肾单位丢失的动物模型中观察到的那样。

方法

在因肾脏捐献导致的肾单位丢失(评估活体肾脏捐献者的长期结局队列)或进行性慢性肾脏病(CKD;饮食改良评估肾脏病研究[MDRD]、非裔美国人肾脏病研究[AASK]和慢性肾功能不全队列[CRIC]研究)的情况下,测量肾小球净蛋白通透性的变化,定义为每毫升每分钟 GFR 的蛋白尿或白蛋白尿。

结果

在肾脏捐献后,肾白蛋白通透性比捐献前增加了 31%(p<0.001)。随着 CKD 的进展,残余 GFR 丢失 50%,MDRD、AASK 和 CRIC 队列中每毫升每分钟 GFR 的蛋白尿分别增加了 1.8 倍、2.1 倍和 1.6 倍(所有均 p<0.001),与收缩压和 ACEi/ARB 使用的变化无关。GFR 降低 70%与相同队列中通透性增加 3.1 倍、4.4 倍和 2.6 倍相关。在 MDRD 参与者中,随着非肾小球原发性疾病的进展,最终通透性的第 75 个百分位数为 141mg/24 h 蛋白尿每毫升每分钟 GFR。如果在基线平均 GFR 为 40ml/min 时存在这种程度的通透性,则会导致肾病范围内的蛋白尿,表明随着 GFR 下降,肾小球发生了新的病理变化。随着 CKD 的进展,在基线时患有肾病综合征的参与者中,通透性也随之增加。因此,尽管大量的功能性肾单位丢失发生了蛋白漏出,但这些参与者的 24 小时蛋白尿或血清白蛋白并没有明显改善。在 GFR 没有下降的情况下,任何队列的通透性都没有增加。

结论

即使没有原发性肾小球疾病,肾单位丢失也会伴随着肾蛋白通透性的增加。这与人类 CKD 中的残余肾单位效应一致。

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