Division of Nephrology, Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
Department of Pediatrics, Section of Nephrology, Yale University School of Medicine, New Haven, Connecticut.
JAMA Pediatr. 2015 Jun;169(6):583-91. doi: 10.1001/jamapediatrics.2015.54.
Research has identified improved biomarkers of acute kidney injury (AKI). Cystatin C (CysC) is a better glomerular filtration rate marker than serum creatinine (SCr) and may improve AKI definition.
To determine if defining clinical AKI by increases in CysC vs SCr alters associations with biomarkers and clinical outcomes.
DESIGN, SETTING, AND PARTICIPANTS: Three-center prospective cohort study of intensive care units in New Haven, Connecticut, Cincinnati, Ohio, and Montreal, Quebec, Canada. Participants were 287 patients 18 years or younger without preoperative AKI or end-stage renal disease who were undergoing cardiac surgery. The study dates were July 1, 2007, through December 31, 2009.
For biomarker vs clinical AKI associations, the exposures were first postoperative (0-6 hours after surgery) urine interleukin 18, neutrophil gelatinase-associated lipocalin, kidney injury molecule 1, and liver fatty acid-binding protein. For clinical AKI outcome associations, the exposure was Kidney Disease: Improving Global Outcomes AKI definition (based on SCr or CysC).
Clinical AKI, length of stay, and length of mechanical ventilation. We determined areas under the receiver operating characteristic curve and odds ratios for first postoperative biomarkers to predict AKI.
The SCr-defined vs CysC-defined AKI incidence differed substantially (43.6% vs 20.6%). Percentage agreement was 71% (κ = 0.38); stage 2 or worse AKI percentage agreement was 95%. Interleukin 18 and kidney injury molecule 1 discriminated for CysC-defined AKI better than for SCr-defined AKI. For interleukin 18 and kidney injury molecule 1, the areas under the receiver operating characteristic curve were 0.74 and 0.65, respectively, for CysC-defined AKI, and 0.66 and 0.58, respectively, for SCr-defined AKI. Fifth (vs first) quintile concentrations of both biomarkers were more strongly associated with CysC-defined AKI. For interleukin 18 and kidney injury molecule 1, the odds ratios were 16.19 (95% CI, 3.55-73.93) and 6.93 (95% CI, 1.88-25.59), respectively, for CysC-defined AKI vs 6.60 (95% CI, 2.76-15.76) and 2.04 (95% CI, 0.94-4.38), respectively, for SCr-defined AKI. Neutrophil gelatinase-associated lipocalin and liver fatty acid-binding protein associations with both definitions were similar. The CysC definitions and SCr definitions were similarly associated with clinical outcomes of resource use.
Compared with the SCr-based definition, the CysC-based definition is more strongly associated with urine interleukin 18 and kidney injury molecule 1 in children undergoing cardiac surgery. Consideration should be made for defining AKI based on CysC in clinical care and future studies.
研究已经确定了急性肾损伤(AKI)的改进生物标志物。胱抑素 C(CysC)是肾小球滤过率的比血清肌酐(SCr)更好的标志物,并且可能改善 AKI 的定义。
确定通过 CysC 与 SCr 的增加来定义临床 AKI 是否会改变与生物标志物和临床结果的关联。
设计、地点和参与者:这是一项在康涅狄格州纽黑文、俄亥俄州辛辛那提和加拿大魁北克省蒙特利尔的三个中心的 ICU 进行的前瞻性队列研究。参与者为 287 名年龄在 18 岁以下、无术前 AKI 或终末期肾病的接受心脏手术的患者。研究日期为 2007 年 7 月 1 日至 2009 年 12 月 31 日。
对于生物标志物与临床 AKI 关联,暴露是术后(手术后 0-6 小时)尿液白细胞介素 18、中性粒细胞明胶酶相关脂质运载蛋白、肾损伤分子 1 和肝脂肪酸结合蛋白。对于临床 AKI 结局关联,暴露是肾脏病:改善全球结局 AKI 定义(基于 SCr 或 CysC)。
临床 AKI、住院时间和机械通气时间。我们确定了接受者操作特征曲线下的面积和优势比,以预测术后第一时间的生物标志物 AKI。
基于 SCr 的 AKI 定义与基于 CysC 的 AKI 定义的发生率差异很大(43.6% vs 20.6%)。百分比一致性为 71%(κ=0.38);2 期或更严重 AKI 的百分比一致性为 95%。白细胞介素 18 和肾损伤分子 1 对 CysC 定义的 AKI 的区分优于对 SCr 定义的 AKI。对于白细胞介素 18 和肾损伤分子 1,接受者操作特征曲线下的面积分别为 0.74 和 0.65,用于 CysC 定义的 AKI,分别为 0.66 和 0.58,用于 SCr 定义的 AKI。两种生物标志物的第五(与第一)五分位数浓度与 CysC 定义的 AKI 相关性更强。对于白细胞介素 18 和肾损伤分子 1,CysC 定义的 AKI 的比值比分别为 16.19(95%置信区间,3.55-73.93)和 6.93(95%置信区间,1.88-25.59),而 SCr 定义的 AKI 分别为 6.60(95%置信区间,2.76-15.76)和 2.04(95%置信区间,0.94-4.38)。中性粒细胞明胶酶相关脂质运载蛋白和肝脂肪酸结合蛋白与两种定义的关联相似。CysC 定义和 SCr 定义与临床结局资源使用具有相似的相关性。
与基于 SCr 的定义相比,基于 CysC 的定义与接受心脏手术的儿童尿液白细胞介素 18 和肾损伤分子 1 的关联更强。在临床护理和未来研究中,应考虑基于 CysC 定义 AKI。