文章摘要
李 波,邵素花,万娅莉,朱果果,余治国.血清尿调节素、肝素结合蛋白、Klotho蛋白联合APACHEⅡ评分对脓毒症并发急性肾损伤患者28天预后的评估价值[J].,2022,(16):3107-3111
血清尿调节素、肝素结合蛋白、Klotho蛋白联合APACHEⅡ评分对脓毒症并发急性肾损伤患者28天预后的评估价值
Evaluation Value of Serum Uromodulin, Heparin-Binding Protein, Klotho Protein Combined with APACHE Ⅱ Score in 28-Day Prognosis in Patients with Sepsis Complicated with Acute Kidney Injury
投稿时间:2022-01-27  修订日期:2022-02-22
DOI:10.13241/j.cnki.pmb.2022.16.022
中文关键词: 脓毒症  急性肾损伤  尿调节素  肝素结合蛋白  Klotho蛋白  APACHEⅡ评分
英文关键词: Sepsis  Acute kidney injury  Uromodulin  Heparin-binding protein  Klotho protein  APACHE Ⅱ Score
基金项目:湖北省卫计委指导性项目(WJ2017F0049)
作者单位E-mail
李 波 中部战区总医院急诊医学科 湖北 武汉 430070 libo4078@163.com 
邵素花 中部战区总医院急诊医学科 湖北 武汉 430070  
万娅莉 中部战区总医院急诊医学科 湖北 武汉 430070  
朱果果 中部战区总医院急诊医学科 湖北 武汉 430070  
余治国 中部战区总医院急诊医学科 湖北 武汉 430070  
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中文摘要:
      摘要 目的:探讨血清尿调节素(UMOD)、肝素结合蛋白(HBP)、Klotho蛋白联合急性生理和慢性健康状况评估系统Ⅱ(APACHEⅡ)评分预测脓毒症并发急性肾损伤(AKI)患者28天预后的价值。方法:选取2018年1月至2020年1月期间我院诊治的脓毒症并发AKI患者120例作为研究对象,根据28天以内的生存情况分为存活组(86例)和死亡组(34例)。采用酶联免疫吸附实验检测各组血清UMOD、HBP、Klotho蛋白表达水平。比较不同分期的AKI患者血清UMOD、HBP、Klotho蛋白表达及APACHEⅡ评分差异。多因素Logistic回归分析影响脓毒症并发AKI患者28天预后的危险因素。应用受试者工作特征(ROC)曲线分析血清UMOD、HBP、Klotho蛋白及APACHEⅡ评分单独及联合预测脓毒症并发AKI患者28天预后的价值。结果:相比于存活组,死亡组患者血清UMOD、Klotho较低,降钙素原(PCT)、超敏C反应蛋白(hs-CRP)、HBP、APACHEⅡ评分较高 (P均<0.05)。不同AKI分期患者血清UMOD、HBP、Klotho及APACHEⅡ评分差异具有统计学意义(P均<0.05)。多因素Logistic回归分析显示UMOD<62.43 mg/mL、HBP>30.14 μg/L、Klotho≤180.37 ng/L、APACHEⅡ评分>16.00分是影响患者28天死亡预后的危险因素。血清UMOD、HBP、Klotho、APACHEⅡ评分四者联合预测脓毒症并发AKI患者28天死亡的曲线下面积为0.897(0.842~0.939),明显高于血清UMOD[0.724(0.674~0.765)]、HBP[0.666(0.622~0.710)]、Klotho[0.767(0.731~0.804)]、APACHEⅡ评分[0.840(0.802~0.878)]单一检测 。结论:脓毒症并发AKI患者血清UMOD、Klotho降低,HBP水平升高且APACHEⅡ评分较高,与脓毒症并发AKI患者的病情严重程度有关,四者联合能辅助预测脓毒症并发AKI患者28天死亡。
英文摘要:
      ABSTRACT Objective: To investigate the value of serum uromodulin (UMOD), heparin-binding protein (HBP), Klotho protein combined with Acute physiology and chronic health evaluation system II (APACHE II) score in predicting the 28-day prognosis in patients with sepsis complicated with acute kidney injury (AKI). Methods: 120 patients with sepsis complicated with AKI who were diagnosed and treated in our hospital from January 2018 to January 2020 were selected as the research object. According to the survival within 28 days, they were divided into survival group (86 cases) and death group (34 cases). Enzyme linked immunosorbent assay was used to detect the expression levels of serum UMOD, HBP and Klotho proteins in each group. The expression of serum UMOD, HBP, Klotho protein and APACHEⅡ score difference in patients with AKI at different stages were compared. Multivariate Logistic regression analysis was used to analyze the risk factors affecting the 28 day prognosis of patients with sepsis complicated with AKI. The receiver operating characteristic (ROC) curve was used to analyze the value of serum UMOD, HBP, Klotho protein and APACHEⅡ score alone and in combination in predicting the 28 day prognosis of patients with sepsis complicated with AKI. Results: Compared with the survival group, the serum UMOD and Klotho in the death group were lower, and the procalcitonin (PCT), high-sensitivity C-reactive protein (hs-CRP), HBP and APACHEⅡ scores were higher (all P<0.05). There were significant differences in the serum UMOD, HBP, Klotho and APACHEⅡ scores in patients with different AKI stages (all P<0.05). Multivariate Logistic regression analysis showed that UMOD < 62.43 mg/mL and HBP > 30.14 ?滋g/L, Klotho ≤ 180.37 ng/L and APACHEⅡ score > 16.00 scores were the risk factors affecting the prognosis of 28 day death. The area under the curve of the combined prediction of serum UMOD, HBP, Klotho and APACHE Ⅱ score for 28 day death in patients with sepsis complicated with AKI was 0.897 (0.842 ~ 0.939), which was significantly higher than that of the single detection of serum UMOD [0.724 (0.674 ~ 0.765)], HBP [0.666 (0.622 ~ 0.710)], Klotho [0.767 (0.731 ~ 0.804)] and APACHEⅡ score [0.840 (0.802 ~ 0.878)]. Conclusion: Serum UMOD and Klotho decrease, HBP level increases and APACHE II score is higher in patients with sepsis complicated with AKI, which are related to the severity of sepsis complicated with AKI. The combination of the four can help to predict 28 days death of sepsis complicated with AKI.
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