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尿 L 型脂肪酸结合蛋白作为重症监护中的新型肾脏生物标志物。

Urinary L-type fatty acid-binding protein as a new renal biomarker in critical care.

机构信息

Department of Nephrology & Endocrinology, University Hospital, The University of Tokyo, Tokyo, Japan.

出版信息

Curr Opin Crit Care. 2010 Dec;16(6):545-9. doi: 10.1097/MCC.0b013e32833e2fa4.

Abstract

PURPOSE OF REVIEW

Acute kidney injury (AKI) remarkably increases the mortality of critically ill patients treated in ICUs. Recently, several renal biomarkers have been developed for the early detection of AKI. We review the potential of urinary L-type fatty acid-binding protein (L-FABP) as a new renal biomarker for AKI diagnosis in critical care.

RECENT FINDINGS

In the kidney, L-FABP is expressed in renal proximal tubular epithelial cells and shed into urine rapidly in response to renal insults. By using human L-FABP transgenic mice, we reported that urinary L-FABP can detect AKI sensitively and reflect its severity accurately in animal models of AKI and sepsis. In clinical evaluations, the good performance of urinary L-FABP was demonstrated not only in pediatric postcardiopulmonary bypass surgery AKI and contrast media-induced AKI but also in septic shock patients complicated with AKI.

SUMMARY

Recent data suggest that urinary L-FABP can contribute to the development of new AKI diagnostic tools in critical care. Combining with other renal markers such as neutrophil gelatinase-associated lipocalin (NGAL) and kidney injury molecule-1 (KIM-1), optimal threshold determination for distinguishing AKI from chronic renal failure should be explored before translation to the clinical.

摘要

目的综述

急性肾损伤(AKI)显著增加了 ICU 中危重症患者的死亡率。最近,已经开发出几种肾生物标志物来早期检测 AKI。我们综述了尿 L 型脂肪酸结合蛋白(L-FABP)作为 AKI 诊断的新肾生物标志物在重症监护中的应用潜力。

最新发现

在肾脏中,L-FABP 表达于肾近端小管上皮细胞,在肾损伤时迅速分泌到尿液中。通过使用人 L-FABP 转基因小鼠,我们发现尿 L-FABP 可以在 AKI 和脓毒症动物模型中敏感地检测 AKI,并准确反映其严重程度。在临床评估中,尿 L-FABP 的良好性能不仅在儿科体外循环术后 AKI 和造影剂诱导的 AKI 中得到了证实,而且在伴有 AKI 的脓毒性休克患者中也得到了证实。

总结

最近的数据表明,尿 L-FABP 可能有助于开发重症监护中 AKI 的新诊断工具。在将其转化为临床应用之前,应与中性粒细胞明胶酶相关脂质运载蛋白(NGAL)和肾损伤分子-1(KIM-1)等其他肾标志物结合,探索区分 AKI 与慢性肾衰竭的最佳阈值。

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