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血浆中性粒细胞明胶酶相关载脂蛋白(NGAL)的预测性能随急性肾损伤程度的增加而提高。

The predictive performance of plasma neutrophil gelatinase-associated lipocalin (NGAL) increases with grade of acute kidney injury.

机构信息

Department of Intensive Care, Austin Health, Melbourne, Australia.

出版信息

Nephrol Dial Transplant. 2009 Nov;24(11):3349-54. doi: 10.1093/ndt/gfp234. Epub 2009 May 27.

Abstract

BACKGROUND

In adult cardiac surgery, the predictive value for AKI of neutrophil gelatinase-associated lipocalin (NGAL) appears to have wide variability. The choice of definition of acute kidney injury (AKI) might, at least in part, account for such variability.

METHODS

In a prospective study of 100 adult cardiac surgery patients, we assessed the value of postoperative plasma NGAL in predicting AKI according to the degree of severity used for its definition.

RESULTS

The predictive value of plasma NGAL varied according to the AKI definition used and was higher for more severe AKI (increase in creatinine >50%: mean AUC-ROC 0.79 +/- 0.01) compared to less severe AKI (>25%: mean AUC-ROC 0.65 +/- 0.02); P = 0.001. The discriminatory ability of NGAL for AKI also increased with increasing RIFLE classes (AUC-ROC R: 0.72, I: 0.79, F: 0.80) or AKIN stages (AUC-ROC 1: 0.75, 2: 0.78, 3: 0.81); P = 0.015. It was highest for the prediction of renal replacement therapy (AUC-ROC: 0.83).

CONCLUSIONS

In adult cardiac surgery patients, the predictive value of NGAL increases with grade of AKI. This observation needs to be taken into account when interpreting any future studies of this biomarker.

摘要

背景

在成人心脏手术中,中性粒细胞明胶酶相关脂质运载蛋白(NGAL)对急性肾损伤(AKI)的预测价值似乎差异很大。AKI 定义的选择可能至少部分解释了这种差异。

方法

在一项对 100 名成年心脏手术患者的前瞻性研究中,我们评估了术后血浆 NGAL 在预测 AKI 中的价值,其预测价值取决于 AKI 定义的严重程度。

结果

血浆 NGAL 的预测价值取决于使用的 AKI 定义,对于更严重的 AKI(肌酐升高>50%:平均 AUC-ROC 0.79 +/- 0.01)比轻度 AKI(升高>25%:平均 AUC-ROC 0.65 +/- 0.02)更高;P = 0.001。NGAL 对 AKI 的鉴别能力也随着 RIFLE 分级(AUC-ROC R:0.72,I:0.79,F:0.80)或 AKIN 分期(AUC-ROC 1:0.75,2:0.78,3:0.81)的增加而增加;P = 0.015。对于预测肾脏替代治疗(AUC-ROC:0.83),其预测价值最高。

结论

在成年心脏手术患者中,NGAL 的预测价值随着 AKI 程度的增加而增加。在解释该生物标志物的任何未来研究时,都需要考虑到这一观察结果。

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