实用肝脏病杂志 ›› 2026, Vol. 29 ›› Issue (2): 249-252.doi: 10.3969/j.issn.1672-5069.2026.02.022

• 肝硬化 • 上一篇    下一篇

MELD评分联合血清胱抑素C和ALBI评分诊断失代偿期肝硬化患者并发肝肾综合征价值研究*

孙博汉, 曹春莉, 奇丽娜   

  1. 010000 呼和浩特市 内蒙古医科大学第一附属医院消化内科
  • 收稿日期:2025-07-12 出版日期:2026-03-10 发布日期:2026-03-13
  • 通讯作者: 曹春莉,E-mail:1026713823@qq.com
  • 作者简介:孙博汉,男,27岁,硕士研究生。E-mail:17320020948@163.com
  • 基金资助:
    *内蒙古自治区自然科学基金资助项目(编号:2025QN08125)

Predictive efficacy of serum cystatin C, MELD and ALBI score combination for hepatorenal syndrome-acute kidney injury in patients with decompendated liver cirrhosis

Sun Bohan, Cao Chunli, Qi Lina   

  1. Department of Gastroenterology, First Affiliated Hospital, Inner Mongolia Medical University, Hohhot 010000, Inner Mongolia Autonomous Region, China
  • Received:2025-07-12 Online:2026-03-10 Published:2026-03-13

摘要: 目的 探讨终末期肝病模型(MELD)评分、白蛋白-胆红素(ALBI)评分和血清胱抑素C(Cys-C)联合预测失代偿期肝硬化并发肝肾综合征-急性肾损伤(HRS-AKI)的价值。方法 2020年10月~2025年4月我院收治的HRS-AKI患者99例和失代偿肝硬化住院患者117例,应用医院信息管理(HIS)系统收集临床基线资料、血生化指标和血清Cys-C水平,计算MELD和ALBI评分。应用二元Logistic 回归分析影响并发HRS-AKI的因素,应用受试者工作特征曲线(ROC)评估各指标对HRS-AKI的诊断效能。结果 99例住院期间发生HRS-AKI患者血清Cys-C水平、MELD评分和ALBI评分分别为2.4(1.6,3.3)mg/L、19.9(11.8,24.3)和-1.1(-1.5,-0.6),均显著高于肝硬化组【分别为1.1(0.9,1.4)mg/L、10.9(7.4,14.5)和-1.4(-1.5,-0.9),P<0.05】;Logistic回归分析显示,凝血酶原时间是影响肝硬化患者并发HRS-AKI的保护因素(OR=0.852,95%CI=0.752~0.964,P<0.05),而血清Cys-C(OR=42.318,95%CI=13.179~135.888,P<0.001)、MELD评分(OR=25.539,95%CI=4.266~152.892,P<0.001)和并发肝性脑病(OR=4.527,95%CI=1.283~15.969,P<0.05)是独立危险因素;ROC分析显示,血清Cys-C联合MELD评分和ALBI评分诊断HRS-AKI的AUC为0.918(95%CI:0.877~0.959),其效能较高。结论 监测血清Cys-C水平联合MELD评分和ALBI评分可以帮助临床医师更加明确诊断住院的失代偿肝硬化患者并发HRS-AKI,值得进一步研究。

关键词: 肝硬化, 肝肾综合征, 胱抑素C, 终末期肝病模型, 白蛋白-胆红素评分, 诊断

Abstract: Objective The purpose of this study was to investigate the diagnosticefficacy of serum cystatin C (Cys-C), model for end-stage liver disease (MELD) and albumin-bilirubin (ALBI) score combination for hepatorenal syndrome-acute kidney injury (HRS-AKI) in patients with decompendated liver cirrhosis (DLC). Methods 99 patients with HRS-AKI and 117 hospitalized patients with DLC were encountered in our hospital between October 2020 and April 2025, baseline clinical materials,serum biochemical index and serum Cys-C levels were collectedby retrieving our hospital information management (HIS) system, and MELD and ALBI scores were calculated. Binary Logistic regression analysis was appliedto identify factors influencing the occurrence of HRS-AKI, and receiver operating characteristic (ROC) curves were employed to evaluate the diagnostic efficacy for HRS-AKI. Results Serum Cys-C levels, MELD and ALBI scores in patients with HRS-AKI were 2.4 (1.6, 3.3) mg/L, 19.9 (11.8, 24.3) and -1.1 (-1.5, -0.6), all significantly higher than [1.1 (0.9, 1.4) mg/L, 10.9 (7.4, 14.5) and -1.4 (-1.5, -0.9), respectively, P<0.05] in the cirrhosis group; Logistic regression analysis revealed that prothrombin time was a protective factor against HRS-AKI in patients with DLC (OR = 0.852, 95% CI = 0.752-0.964, P<0.05), while serum Cys-C level (OR = 42.318, 95% CI = 13.179-135.888, P<0.05), MELD score (OR = 25.539, 95% CI = 4.266-152.892, P<0.05) and concurrent hepatic encephalopathy (OR = 4.527, 95% CI = 1.283-15.969, P<0.05) were the independent risk factors; ROC analysis showed that the AUC was 0.918 (95% CI: 0.877-0.959), when combination of serum Cys-C level, MELD and ALBI score was set for diagnosing HRS-AKI. Conclusion Serum Cys-C levels in combination with MELD and ALBI scores could assist clinicians for the early diagnosis of HRS-AKI in hospitalized patientswith DLC, which warrants further study.

Key words: Liver cirrhosis, Hepatorenal syndrome, Cystatin C, Model for end-stage liver disease, Albumin-bilirubin score, Diagnosis