中性粒细胞明胶酶相关脂钙蛋白作为术前肾损害患者心脏手术后急性肾损伤的标志物

N Tidbury, N Browning, M Shaw, M Morgan, I Kemp, B Matata
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引用次数: 5

摘要

急性肾损伤(AKI)是心脏手术的严重并发症。目前确定AKI的“金标准”是血清肌酐和尿量的变化,然而,这种变化发生在实际损伤发生后相对较晚。需要发现新的生物标志物来检测早期AKI。最近,新的生物标志物,如NephroCheck®Test和AKIRisk也被测试并发现是AKI的良好指标。中性粒细胞明胶酶相关脂钙蛋白(NGAL)在儿科患者中显示出希望,但在成人人群中显示出不同的结果,特别是在心脏手术后。本研究的目的是评估尿NGAL作为预先存在肾损害患者(eGFR >15ml/min to eGFR) AKI生物标志物的价值。方法:对125例预先存在肾损害患者的尿NGAL浓度进行事后分析,这些患者参加了一项心脏手术期间血液滤过的随机试验。在基线、术后及术后24、48小时采用ELISA法测定尿NGAL,在术前、术后及术后24、48、72、96小时作为常规患者护理时测定血清肌酐。通过血清肌酐浓度的变化,比较AKI患者和非AKI患者的NGAL浓度。Kaplan-Meier图比较有或无AKI患者的生存率,并进行Cox比例风险分析,以确定对生存率影响最大的因素。结果:手术后,43%的患者发生AKI(基于KDIGO定义)。基线尿NGAL在发生AKI和未发生AKI的患者之间没有显著差异。手术后所有患者的尿NGAL浓度均升高,无论他们是否发生AKI,并且在24小时(p=0.003)和48小时(p156ng/mL)组之间也显着升高(p156ng/mL也强烈预测7年生存率)。然而,与术后48小时尿NGAL >156ng/mL相比,EuroSCORE、年龄、当前吸烟和术后抗生素使用对7年生存的预测能力明显更强。结论:我们的研究表明,术后48小时尿NGAL水平可以根据术前肾损害患者的KDIGO分类强烈预测术后AKI的发生或严重程度,并与7年生存率密切相关。
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Neutrophil Gelatinase-associated Lipocalin as a Marker of Postoperative Acute Kidney Injury Following Cardiac Surgery in Patients with Preoperative Kidney Impairment.

Introduction: Acute kidney injury (AKI) is a serious complication of cardiac surgery. The current 'gold standard' for determining AKI is change in serum creatinine and urine output, however, this change occurs relatively late after the actual injury occurs. Identification of new biomarkers that detect early AKI is required. Recently, new biomarkers, such as the NephroCheck® Test and AKIRisk have also been tested and found to be good indicators of AKI. Neutrophil gelatinase-associated lipocalin (NGAL) has shown promise in paediatric patients but has displayed varied results in adult populations, particularly post cardiac surgery. The aim of this study was to assess the value of urinary NGAL as a biomarker of AKI in patients with pre-existing renal impairment (eGFR >15ml/min to eGFR<60ml/min).

Methods: A post-hoc analysis of urinary NGAL concentrations from 125 patients with pre-existing kidney impairment, who participated in a randomised trial of haemofiltration during cardiac surgery, was undertaken. Urinary NGAL was measured using ELISA at baseline, post-operatively and 24 and 48 hours after surgery, and serum creatinine was measured pre and postoperatively and then at 24, 48, 72 and 96 hours as routine patient care. NGAL concentrations were compared in patients with and without AKI determined by changes in serum creatinine concentrations. A Kaplan-Meier plot compared survival for patients with or without AKI and a Cox proportional hazards analysis was performed to identify factors with the greatest influence on survival.

Results: Following surgery, 43% of patients developed AKI (based on KDIGO definition). Baseline urinary NGAL was not found to be significantly different between patients that did and did not develop AKI. Urinary NGAL concentration was increased in all patients following surgery, regardless of whether they developed AKI and was also significant between groups at 24 (p=0.003) and 48 hours (p<0.0001). Urinary NGAL concentrations at 48 hours correlated with serum creatinine concentrations at 48 hours (r=0.477, p<0.0001), 72 hours (r=0.488, p<0.0001) and 96 hours (r=0.463, p<0.0001). Urinary NGAL at 48 hours after surgery strongly predicted AKI (AUC=0.76; P=0.0001). A Kaplan- Meier plot showed that patients with postoperative AKI had a significantly lower 7-year survival compared with those without AKI. Postoperative urinary NGAL at 48 hours >156ng/mL also strongly predicted 7-year survival. However, additive EuroSCORE, age, current smoking and post-operative antibiotics usage were distinctly significantly more predictive of 7-year survival as compared with postoperative urinary NGAL at 48 hours >156ng/mL.

Conclusions: Our study demonstrated that postoperative urinary NGAL levels at 48 hours postsurgery strongly predicts the onset or severity of postoperative AKI based on KDIGO classification in patients with preoperative kidney impairment and were also strongly related to 7-year survival.

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来源期刊
Cardiovascular and Hematological Disorders - Drug Targets
Cardiovascular and Hematological Disorders - Drug Targets Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.90
自引率
0.00%
发文量
36
期刊介绍: Cardiovascular & Hematological Disorders - Drug Targets aims to cover all the latest and outstanding developments on the medicinal chemistry, pharmacology, molecular biology, genomics and biochemistry of contemporary molecular targets involved in cardiovascular and hematological disorders e.g. disease specific proteins, receptors, enzymes, genes. Each issue of the journal contains a series of timely in-depth reviews written by leaders in the field covering a range of current topics on drug targets involved in cardiovascular and hematological disorders. As the discovery, identification, characterization and validation of novel human drug targets for cardiovascular and hematological drug discovery continues to grow.
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