Objective: To investigate the early predictive value of serum or urinary neutrophil gelatinase-associated lipocalin(NGAL), kidney injury molecule-1(KIM-1) and cystatin(CysC) for acute kidney injury(AKI) in neonates with late-onset sepsis(LOS). Methods: A total of 120 LOS neonates admitted to our hospital from October 2017 to December 2019 were retrospectively analyzed and divided into AKI group(n=23) and non-AKI group(n=97) according to modified AKIN staging system. Serum and urine samples were collected at 0, 12, 24 and 48 h after admission. The expressions of NGAL, KIM-1 and CysC in serum and urine were detected by ELISA method. The receiver operating characteristic(ROC) curve was drawn to evaluate the predictive value of NGAL, KIM-1 and CysC in serum and urine at admission for early AKI in neonates with LOS. Multivariate Logistic regression was used to analyze the risk factors of secondary AKI in neonates with LOS. Results: Within 2 days after admission, the levels of NGAL, KIM-1 and CysC in serum and urine of AKI group were higher than those of non-AKI group(P<0.05). According to AKI staging standard, the levels of serum NGAL and urinary NGAL, KIM-1 in Grade Ⅲ group(n=4) were higher than that in Grade Ⅰ group(n=12) (P<0.05). Multivariate Logistic regression showed that urinary NGAL(OR=6.507, 95% CI 1.899-17.431), KIM-1(OR=2.304, 95% CI 1.385-5.496) and CysC(OR=1.420, 95% CI 1.097-2.641) were independent risk factors for secondary AKI in neonates with LOS(P<0.05). The area under ROC curve(AUC) of urinary NGAL was higher than that of serum NGAL(P<0.05). There was no significant difference in AUC value of KIM-1 or CysC in serum and urine samples(P>0.05). By Spearman analysis, the correlation between urinary NGAL and actual results was higher than that of serum NGAL(rs=0.588, P<0.05). In addition, by H-L goodness of fit test, serum and urinary NGAL, KIM-1, CysC had a good fit with the actual results(all P>0.05). Conclusion: Serum and urinary NGAL, KIM-1 and CysC have certain early predictive value for AKI in neonates with LOS, and urinary NGAL has the highest predictive effect. |
[1] ALCOCK G,LILEY H G,COOKE L,et al.Prevention of neonatal late-onset sepsis:a randomised controlled trial[J].BMC Pediatr,2017,17(1):98.
[2] VLACHOPANOS G,SCHIZAS D,HASEMAKI N,et al.Pathophysiology of contrast-induced acute kidney injury(CIAKI)[J].Curr Pharm Des,2019,25(44):4642-4647.
[3] 张伟,于文娟,陈云庆,等.免疫组织化学在具有嗜酸细胞形态肾肿瘤鉴别诊断中的作用[J].中华病理学杂志,2016,45(10):692-697.
[4] XIAO X,TANG R,ZHOU X,et al.Aldosterone induces NRK-52E cell apoptosis in acute kidney injury via rno-miR-203 hypermethylation and Kim-1 upregulation[J].Exp Ther Med,2016,12(2):915-924.
[5] 徐茂青,钟祥薇,李萍,等.NGAL、CysC、β2-MG和SCr联合检测在妊娠期高血压早期肾损伤诊断中的应用价值[J].当代医学,2020,26(25):71-73.
[6] SHANE A L,SÁNCHEZ P J,STOLL B J.Neonatal sepsis[J].Lancet,2017,390(10104):1770-1780.
[7] MEMAR M Y,ALIZADEH N,VARSHOCHI M,et al.Immunologic biomarkers for diagnostic of early-onset neonatal sepsis[J].J Matern Fetal Neonatal Med,2019,32(1):143-153.
[8] GOWDA H,NORTON R,WHITE A,et al.Late-onset Neonatal Sepsis-A 10-year Review From North Queensland,Australia[J].Pediatr Infect Dis J,2017,36(9):883-888.
[9] CHARLTON J R,BOOHAKER L,ASKENAZI D,et al.Late onset neonatal acute kidney injury:results from the AWAKEN Study[J].Pediatr Res,2019,85(3):339-348.
[10] SWEETMAN D U.Neonatal acute kidney injury-Severity and recovery prediction and the role of serum and urinary biomarkers[J].Early Hum Dev,2017,105:57-61.
[11] LEVEY A S,JAMES M T.Acute kidney injury[J].Ann Intern Med,2017,167(9):ITC66-ITC80.
[12] UENO K,SEKI S,SHIOKAWA N,et al.Validation of acute kidney injury according to the modified KDIGO criteria in infants after cardiac surgery for congenital heart disease[J].Nephrology(Carlton),2019,24(3):294-300.
[13] MOLEDINA D G,PARIKH C R.Phenotyping of acute kidney injury:beyond serum creatinine[J].Semin Nephrol,2018,38(1):3-11.
[14] EL-FARGHALI O G,EL-RAGGAL N M,MAHMOUD N H,et al.Serum neutrophil gelatinase-associated lipocalin as a predictor of acute kidney injury in critically-ill neonates[J].Pak J Biol Sci,2012,15(5):231-237.
[15] SHANG W,WANG Z.The update of NGAL in acute kidney injury[J].Curr Protein Pept Sci,2017,18(12):1211-1217.
[16] YANG L,BROOKS C R,XIAO S,et al.KIM-1-mediated phagocytosis reduces acute injury to the kidney[J].J Clin Invest,2015,125(4):1620-1636.
[17] ZHANG L,SUN J,ZHANG M,et al.The significance of combined detection of CysC,urinary mAlb and β2-MG in diagnosis of the early renal injury in pregnancy-induced hypertension syndrome[J].Saudi J Biol Sci,2019,26(8):1982-1985.
[18] 葛斌,刘艳,徐革,等.建立NGAL诊断阈值有利于临床判断和发现急性肾功能损伤[J].基因组学与应用生物学,2019,26(3):1434-1441. |