Herget-Rosenthal S, Metzger J, Albalat A, Bitsika V, Mischak H
Department of Medicine and Nephrology,Rotes Kreuz Krankenhaus, Bremen, Germany.
Prilozi. 2012;33(1):27-48.
Acute kidney injury (AKI) comprises several syndromes that are associated with a sudden decrease in renal function. AKI is a common condition especially among critically ill patients. It is typically multifactorial and of great prognostic significance. The incidence of AKI has increased while the associated mortality rate has remained unchanged over the last years. Recent definitions of AKI, namely the Risk, Injury, Failure, Loss of renal function and End-stage kidney disease (RIFLE) classifycation or the Acute Kidney Injury Network (AKIN) criteria, incorporate serum creatinine and urine output as the principal markers to define and detect AKI. However, elevated serum creatinine or oliguria were demonstrated to detect AKI at late stages of renal injury when preventive strategies may be less effective. Therefore, there has recently been a great scientific interest in obtainng valuable markers for early AKI detection. In the last 5 years numerous new markers such as neutrophil-gelatinase associated lipo-calin, interleukin-18, cystatin C and kidney injury molecule 1 in the urine and/or serum have been studied and proposed as early detection markers of AKI. Persistently, these markers performed well in initial pilot trials. However, these promising results could often not be confirmed in later, larger multicentre trials and limitation of these biomarkers in the early diagnosis of renal injury were discovered. Furthermore, as AKI is multi-factorial and heterogeneous in origin, it seems likely that not one single marker but a panel of biomarkers will be required to detect all subtypes of AKI early during their evolution. This has initiated proteomic studies to develop panels of biomarkers which may facilitate early detection of AKI. The present review will focus on the most important clinical studies evaluating the ability of single AKI biomarkers and on those in clinical proteomics that attempted to establish panels of biomarkers in urine for early and accurate AKI diagnosis and prognosis.
急性肾损伤(AKI)包括几种与肾功能突然下降相关的综合征。AKI是一种常见病症,尤其在重症患者中。它通常是多因素的,具有重要的预后意义。在过去几年中,AKI的发病率有所上升,而相关死亡率保持不变。最近对AKI的定义,即风险、损伤、衰竭、肾功能丧失和终末期肾病(RIFLE)分类或急性肾损伤网络(AKIN)标准,将血清肌酐和尿量作为定义和检测AKI的主要指标。然而,血清肌酐升高或少尿被证明是在肾损伤晚期检测AKI,此时预防策略可能效果较差。因此,最近在获取用于早期检测AKI的有价值标志物方面产生了浓厚的科学兴趣。在过去5年中,已经研究了许多新的标志物,如尿液和/或血清中的中性粒细胞明胶酶相关脂质运载蛋白、白细胞介素-18、胱抑素C和肾损伤分子1,并将其作为AKI的早期检测标志物提出。持续地,这些标志物在最初的试点试验中表现良好。然而,这些有前景的结果在后来更大规模的多中心试验中往往无法得到证实,并且发现了这些生物标志物在肾损伤早期诊断中的局限性。此外,由于AKI是多因素且起源异质性的,似乎不是单一标志物而是一组生物标志物将需要在其发展早期检测所有AKI亚型。这引发了蛋白质组学研究以开发可能有助于早期检测AKI的生物标志物组。本综述将重点关注评估单一AKI生物标志物能力的最重要临床研究,以及那些临床蛋白质组学中试图建立尿液生物标志物组以进行早期准确的AKI诊断和预后评估的研究。