Department of Pathophysiology, Medical University of Silesia, Katowice, Poland.
Ren Fail. 2012;34(1):130-3. doi: 10.3109/0886022X.2011.623500. Epub 2011 Oct 20.
Neutrophil gelatinase-associated lipocalin (NGAL) has generated great interest as a novel biomarker for the timely detection of acute kidney injury (AKI). Despite the enthusiasm surrounding NGAL, the research so far details and attempts to minimize a host of limitations that substantially preclude its use as a valuable diagnostic biomarker to detect AKI and guide clinical treatment. In our review of the current research, obvious drawbacks such as variable sensitivity and specificity, even among similar patient populations were discovered. Furthermore, there are not well-defined cutoff values among various patient populations which would permit use of NGAL as a positive or negative diagnostic marker similar to troponin in cardiac injury. Moreover, due to the wide variation in baseline concentration of NGAL among patients, the added requirement of serial measurements, that may not even be accurate in at-risk or chronic kidney injury populations, further degrades the benefit of early detection.
中性粒细胞明胶酶相关脂质运载蛋白(NGAL)作为一种新型生物标志物,可用于及时检测急性肾损伤(AKI),引起了广泛关注。尽管 NGAL 备受关注,但迄今为止的研究详细探讨并试图尽量减少其作为有价值的诊断生物标志物检测 AKI 和指导临床治疗的大量局限性。在我们对当前研究的回顾中,发现了明显的缺陷,例如在相似的患者人群中,敏感性和特异性存在差异。此外,不同患者人群之间没有明确的截断值,这使得 NGAL 无法像心肌损伤中的肌钙蛋白一样作为阳性或阴性诊断标志物使用。此外,由于患者 NGAL 的基础浓度差异很大,需要进行连续测量,而在高危或慢性肾损伤患者中,这甚至可能不准确,这进一步降低了早期检测的益处。