College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, Scotland.
Department of Pediatrics and Child Health, Children's Hospital at Health Sciences Center, University of Manitoba, Winnipeg, MB, Canada.
Pediatr Nephrol. 2022 Sep;37(9):2079-2090. doi: 10.1007/s00467-021-05380-6. Epub 2022 Jan 10.
Acute kidney injury (AKI) is characterized by an abrupt decline in glomerular filtration rate (GFR). We sought to identify separate early urinary metabolomic signatures at AKI onset (with-AKI) and prior to onset of functional impairment (pre-AKI).
Pre-AKI (n=15), AKI (n=22), and respective controls (n=30) from two prospective PICU cohort studies provided urine samples which were analyzed by GC-MS and DI-MS mass spectrometry (193 metabolites). The cohort (n=58) was 8.7±6.4 years old and 66% male. AKI patients had longer PICU stays, higher PRISM scores, vasopressors requirement, and respiratory diagnosis and less commonly had trauma or post-operative diagnosis. Urine was collected within 2-3 days after admission and daily until day 5 or 14.
The metabolite classifiers for pre-AKI samples (1.5±1.1 days prior to AKI onset) had a cross-validated area under receiver operator curve (AUC)=0.93 (95%CI 0.85-1.0); with-AKI samples had an AUC=0.94 (95%CI 0.87-1.0). A parsimonious pre-AKI classifier with 13 metabolites was similarly robust (AUC=0.96, 95%CI 0.89-1.0). Both classifiers were similar and showed modest correlation of high-ranking metabolites (tau=0.47, p<0.001).
This exploratory study demonstrates the potential of a urine metabolite classifier to detect AKI-risk in pediatric populations earlier than the current standard of diagnosis with the need for external validation. A higher resolution version of the Graphical abstract is available as Supplementary information with inner reference to ESM for GA.
急性肾损伤(AKI)的特征是肾小球滤过率(GFR)突然下降。我们试图确定 AKI 发作时(有 AKI)和功能损伤前(有 AKI)的单独早期尿代谢组学特征。
来自两项前瞻性 PICU 队列研究的有 AKI(n=22)、无 AKI(n=15)和各自对照(n=30)提供了尿液样本,这些样本通过 GC-MS 和 DI-MS 质谱分析(193 种代谢物)。队列(n=58)年龄为 8.7±6.4 岁,66%为男性。AKI 患者 PICU 停留时间更长,PRISM 评分更高,需要血管加压素,呼吸诊断更常见,创伤或术后诊断较少。尿液采集于入院后 2-3 天内,每天采集直至第 5 天或第 14 天。
有 AKI 前样本的代谢物分类器(在 AKI 发作前 1.5±1.1 天)具有交叉验证的接受者操作特征曲线(ROC)下面积(AUC)=0.93(95%CI 0.85-1.0);有 AKI 样本的 AUC=0.94(95%CI 0.87-1.0)。具有 13 种代谢物的简化有 AKI 分类器同样稳健(AUC=0.96,95%CI 0.89-1.0)。两个分类器相似,并且显示高排名代谢物的适度相关性(tau=0.47,p<0.001)。
这项探索性研究表明,尿液代谢物分类器有可能比当前的诊断标准更早地检测儿科人群的 AKI 风险,需要进行外部验证。更高分辨率版本的图形摘要可作为补充信息提供,其中包含对 ESM 中 GA 的内部参考。