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应用动态磁共振成像测量慢性肾脏病患者的肾小球滤过率。

Measurement of glomerular filtration rate using dynamic magnetic resonance imaging in patients with chronic kidney disease.

机构信息

Department of Internal Medicine IV, Section of Nephrology and Hypertension, University of Tuebingen, Tuebingen, Germany.

出版信息

J Nephrol. 2011 Jul-Aug;24(4):482-9. doi: 10.5301/JN.2010.5978.

Abstract

BACKGROUND

Determination of glomerular filtration rate (GFR) using plasma disappearance curves requires the injection of a filtration marker and repeated timed blood collections. Gadolinium-containing contrast media are excreted exclusively by glomerular filtration and could provide a novel approach to quantifying GFR using magnetic resonance (MR) imaging. The aim of this study was to demonstrate the feasibility of measuring GFR by the clearance of gadolinium-containing contrast medium in patients with chronic kidney disease (CKD).

METHODS

Informed consent was obtained from stable CKD patients in stages 1, 2 or 3 (n=16; 5 women, 11 men; median age 54 years). GFR was measured after a bolus injection of gadobutrol (4 mL, approximately 0.05 mmol/kg) and calculated from the washout of the signal intensity obtained over the liver. The obtained MR-GFR was compared with simultaneously measured plasma clearance of inulin and gadobutrol.

RESULTS

Technical failure occurred in 2 patients. The mean obtained MR-GFR was 71 ± 25 (SD) mL/min per 1.73 m² and agreed well with the mean inulin-GFR (70 ± 24 mL/min per 1.73 m²). Pearson's correlation coefficient was r=0.91. The mean of the paired differences was 1 ± 10 mL/min per 1.73 m² and not significantly different from zero. GFR obtained from gadobutrol plasma clearance also agreed well with inulin-GFR and MR-GFR (r=0.92 and r=0.75, respectively).

CONCLUSIONS

We describe a novel method of determining GFR from MR imaging using a low dose of gadobutrol in patients with reduced GFR that enables the absolute quantification of GFR after routine contrast-enhanced MR imaging.

摘要

背景

使用血浆清除曲线测定肾小球滤过率(GFR)需要注射滤过标志物并重复定时采血。含钆的对比剂仅通过肾小球滤过排泄,可提供一种使用磁共振(MR)成像定量 GFR 的新方法。本研究旨在证明在慢性肾脏病(CKD)患者中通过含钆对比剂的清除来测量 GFR 的可行性。

方法

征得 16 例稳定 CKD 患者(1 期、2 期或 3 期,5 名女性,11 名男性;中位年龄 54 岁)的知情同意。在注射钆布醇(4 毫升,约 0.05mmol/kg)后测量 GFR,并从肝脏信号强度的洗脱中计算。获得的 MR-GFR 与同时测量的菊粉和钆布醇的血浆清除率进行比较。

结果

2 例患者技术失败。获得的平均 MR-GFR 为 71±25(SD)mL/min/1.73m²,与平均菊粉-GFR(70±24mL/min/1.73m²)吻合良好。Pearson 相关系数 r=0.91。配对差异的平均值为 1±10mL/min/1.73m²,与零无显著差异。从钆布醇血浆清除率获得的 GFR 也与菊粉-GFR 和 MR-GFR 吻合良好(r=0.92 和 r=0.75)。

结论

我们描述了一种使用低剂量钆布醇从 MR 成像确定 GFR 的新方法,该方法适用于 GFR 降低的患者,可在常规对比增强 MR 成像后实现 GFR 的绝对定量。

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