CLEAVAGE OF IGFBP-1 BY AN ENZYME IN URINE PREDICTS THE FUTURE NEED FOR KIDNEY REPLACEMENT THERAPY IN ACUTE KIDNEY INJURY.

Q2 Medicine
John M Arthur, Joseph H Holthoff
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引用次数: 0

Abstract

The only Food and Drug Administration (FDA)-approved biomarker for prediction of acute kidney injury (AKI) in adults has a false positive rate (FPR) of 50%. We identified insulin-like growth factor-binding protein 1 (IGFBP-1) as a good but not great predictor of severe AKI. IGFBP-1 was cleaved by an enzyme in the urine. We tested the ability of IGFBP-1 cleavage to predict progression to dialysis. Urine from all 12 patients with stage 1 AKI that progressed to require dialysis cleaved the protein (100% sensitivity). FPR was 0% among healthy controls. FPRs among patients with stage 1 AKI at the time of collection were 11% for patients who did not progress beyond stage 1, 15% for patients who progressed to stage 2, and 50% for patients who progressed to stage 3 but did not require dialysis. The sensitivity of a test with these characteristics would be 100% in a typical intensive care unit (ICU) population, and the FPR would be 6%.

尿中一种酶对igfbp-1的裂解预示着急性肾损伤患者未来需要肾脏替代治疗。
美国食品和药物管理局(FDA)唯一批准的用于预测成人急性肾损伤(AKI)的生物标志物的假阳性率(FPR)为50%。我们发现胰岛素样生长因子结合蛋白1 (IGFBP-1)是严重AKI的良好但不是很好的预测因子。IGFBP-1被尿液中的一种酶裂解。我们测试了IGFBP-1切割预测透析进展的能力。所有12例进展到需要透析的1期AKI患者的尿液都能裂解该蛋白(100%敏感性)。健康对照组FPR为0%。在收集数据时,未进展超过1期的1期AKI患者的FPRs为11%,进展到2期的患者为15%,进展到3期但不需要透析的患者为50%。在典型的重症监护病房(ICU)人群中,具有这些特征的检测灵敏度为100%,FPR为6%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.70
自引率
0.00%
发文量
57
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