Division of Nephrology, Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland.
Section of Nephrology and Clinical and Translational Research Accelerator, Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.
Am J Kidney Dis. 2022 Feb;79(2):257-267.e1. doi: 10.1053/j.ajkd.2021.09.008. Epub 2021 Oct 25.
RATIONALE & OBJECTIVE: Acute kidney injury (AKI) is common in patients with coronavirus disease 2019 (COVID-19) and associated with poor outcomes. Urinary biomarkers have been associated with adverse kidney outcomes in other settings and may provide additional prognostic information in patients with COVID-19. We investigated the association between urinary biomarkers and adverse kidney outcomes among patients hospitalized with COVID-19.
Prospective cohort study.
SETTING & PARTICIPANTS: Patients hospitalized with COVID-19 (n=153) at 2 academic medical centers between April and June 2020.
19 urinary biomarkers of injury, inflammation, and repair.
Composite of KDIGO (Kidney Disease: Improving Global Outcomes) stage 3 AKI, requirement for dialysis, or death within 60 days of hospital admission. We also compared various kidney biomarker levels in the setting of COVID-19 versus other common AKI settings.
Time-varying Cox proportional hazards regression to associate biomarker level with composite outcome.
Out of 153 patients, 24 (15.7%) experienced the primary outcome. Twofold higher levels of neutrophil gelatinase-associated lipocalin (NGAL) (HR, 1.34 [95% CI, 1.14-1.57]), monocyte chemoattractant protein (MCP-1) (HR, 1.42 [95% CI, 1.09-1.84]), and kidney injury molecule 1 (KIM-1) (HR, 2.03 [95% CI, 1.38-2.99]) were associated with highest risk of sustaining primary composite outcome. Higher epidermal growth factor (EGF) levels were associated with a lower risk of the primary outcome (HR, 0.61 [95% CI, 0.47-0.79]). Individual biomarkers provided moderate discrimination and biomarker combinations improved discrimination for the primary outcome. The degree of kidney injury by biomarker level in COVID-19 was comparable to other settings of clinical AKI. There was evidence of subclinical AKI in COVID-19 patients based on elevated injury biomarker level in patients without clinical AKI defined by serum creatinine.
Small sample size with low number of composite outcome events.
Urinary biomarkers are associated with adverse kidney outcomes in patients hospitalized with COVID-19 and may provide valuable information to monitor kidney disease progression and recovery.
急性肾损伤(AKI)在 2019 年冠状病毒病(COVID-19)患者中很常见,与不良预后相关。尿生物标志物与其他情况下的不良肾脏结局相关,并且可能为 COVID-19 患者提供额外的预后信息。我们研究了住院 COVID-19 患者中尿生物标志物与不良肾脏结局之间的关系。
前瞻性队列研究。
2020 年 4 月至 6 月期间,在 2 所学术医疗中心住院的 COVID-19 患者(n=153)。
19 种尿损伤、炎症和修复的生物标志物。
KDIGO(肾脏疾病:改善全球结局)3 期 AKI、需要透析或住院后 60 天内死亡的复合结局。我们还比较了 COVID-19 与其他常见 AKI 情况下的各种肾脏生物标志物水平。
时间变化 Cox 比例风险回归分析,以将生物标志物水平与复合结局相关联。
在 153 例患者中,24 例(15.7%)发生了主要结局。中性粒细胞明胶酶相关脂质运载蛋白(NGAL)(HR,1.34[95%CI,1.14-1.57])和单核细胞趋化蛋白 1(MCP-1)(HR,1.42[95%CI,1.09-1.84])的两倍高水平与发生主要复合结局的最高风险相关。更高的表皮生长因子(EGF)水平与主要结局的风险降低相关(HR,0.61[95%CI,0.47-0.79])。单个生物标志物提供了中度的鉴别能力,而生物标志物组合提高了对主要结局的鉴别能力。根据血清肌酐定义无临床 AKI 的患者中升高的损伤生物标志物水平,COVID-19 患者的生物标志物水平与 AKI 程度相当。
样本量小,复合结局事件数量少。
尿生物标志物与住院 COVID-19 患者的不良肾脏结局相关,并且可能为监测肾脏疾病进展和恢复提供有价值的信息。