Puthumana Jeremy, Ariza Xavier, Belcher Justin M, Graupera Isabel, Ginès Pere, Parikh Chirag R
Program of Applied Translational Research, Department of Medicine, Yale University School of Medicine, New Haven, Connecticut.
Clínic de Barcelona, Universitat de Barcelona, University of Barcelona, Institut d'Investigacions Biomèdiques August-Pi-Sunyer, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Barcelona, Spain.
Clin Gastroenterol Hepatol. 2017 Jul;15(7):1003-1013.e3. doi: 10.1016/j.cgh.2016.11.035. Epub 2016 Dec 21.
BACKGROUND & AIMS: Acute kidney injury (AKI) is a common complication in patients with cirrhosis that increases mortality. The most common causes of AKI in these patients are prerenal azotemia, acute tubular necrosis (ATN), and hepatorenal syndrome; it is important to determine the etiology of AKI to select the proper treatment and predict patient outcome. Urine biomarkers could be used to differentiate between patients with ATN and functional causes of AKI. We performed a systematic review and meta-analysis of published studies to determine whether urine levels of interleukin (IL)18 and lipocalin 2 or neutrophil gelatinase-associated lipocalin (NGAL) are associated with the development of ATN in patients with cirrhosis.
We searched MEDLINE, Scopus, ISI Web of Knowledge, and conference abstracts through December 31, 2015, for studies that assessed urine biomarkers for detection of acute kidney injury in patients with cirrhosis or reported an association between urine biomarkers and all-cause mortality in these patients. We included only biomarkers assessed in 3 or more independent studies, searching for terms that included urine biomarkers, cirrhosis, NGAL, and IL18. We calculated the pooled sensitivities and specificities for detection and calculated the area under the receiver operating characteristic curve (AUC) values using a bivariate logistic mixed-effects model. We used the χ test to assess heterogeneity among studies.
We analyzed data from 8 prospective studies, comprising 1129 patients with cirrhosis. We found urine levels of the markers discriminated between patients with ATN and other types of kidney impairments, with AUC values of 0.88 for IL18 (95% confidence interval [CI], 0.79-0.97) and 0.89 for NGAL (95% CI, 0.84-0.94). Urine levels of IL18 identified patients who would die in the hospital or within 90 days (short-term mortality) with an AUC value of 0.76 (95% CI, 0.68-0.85); NGAL identified these patients with the same AUC (0.76; 95% CI, 0.71-0.82).
In a systematic review and meta-analysis, we found that urine levels of IL18 and NGAL from patients with cirrhosis discriminate between those with ATN and other types of kidney impairments, with AUC values of 0.88 and 0.89, respectively. Urine levels of IL18 and NGAL identified patients with short-term mortality with an AUC value of 0.76. These biomarkers might be used to determine prognosis and select treatments for patients with cirrhosis.
急性肾损伤(AKI)是肝硬化患者常见的并发症,会增加死亡率。这些患者发生AKI最常见的原因是肾前性氮质血症、急性肾小管坏死(ATN)和肝肾综合征;确定AKI的病因对于选择恰当的治疗方法和预测患者预后很重要。尿生物标志物可用于区分ATN患者和AKI的功能性病因。我们对已发表的研究进行了系统评价和荟萃分析,以确定白细胞介素(IL)-18、lipocalin 2或中性粒细胞明胶酶相关lipocalin(NGAL)的尿水平是否与肝硬化患者ATN的发生有关。
我们检索了截至2015年12月31日的MEDLINE、Scopus、ISI Web of Knowledge和会议摘要,以查找评估尿生物标志物用于检测肝硬化患者急性肾损伤的研究,或报告这些患者尿生物标志物与全因死亡率之间关联的研究。我们仅纳入在3项或更多独立研究中评估的生物标志物,搜索词包括尿生物标志物、肝硬化、NGAL和IL-18。我们计算了检测的合并敏感性和特异性,并使用双变量逻辑混合效应模型计算了受试者工作特征曲线(AUC)值下的面积。我们使用χ检验评估研究间的异质性。
我们分析了8项前瞻性研究的数据,包括1129例肝硬化患者。我们发现这些标志物的尿水平可区分ATN患者和其他类型的肾脏损伤,IL-18的AUC值为0.88(95%置信区间[CI],0.79-0.97),NGAL的AUC值为0.89(95%CI,0.84-0.94)。IL-18的尿水平可识别将在医院死亡或在90天内死亡(短期死亡率)的患者,AUC值为0.76(95%CI,0.68-0.85);NGAL识别这些患者的AUC值相同(0.76;95%CI,0.71-0.82)。
在一项系统评价和荟萃分析中,我们发现肝硬化患者IL-18和NGAL的尿水平可区分ATN患者和其他类型的肾脏损伤,AUC值分别为0.88和0.89。IL-18和NGAL的尿水平识别短期死亡率患者的AUC值为0.76。这些生物标志物可用于确定肝硬化患者的预后并选择治疗方法。