Division of Gastro-enterology, Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok 10330, Thailand.
Department of Medicine, Queen Savang Vadhana Memorial Hospital, Chonburi 20110, Thailand.
World J Gastroenterol. 2023 Aug 28;29(32):4873-4882. doi: 10.3748/wjg.v29.i32.4873.
The albumin-bilirubin (ALBI) score is an index of liver function recently developed to assess prognosis in patients with hepatocellular carcinoma (HCC). It can detect small changes in liver dysfunction and has been successfully applied to the prediction of survival in patients with non-malignant liver diseases of various etiologies.
To investigate the ALBI score for identifying decompensation risk at the 3-year follow-up in patients with compensated cirrhosis.
One-hundred and twenty-three patients with compensated cirrhosis without HCC in King Chulalongkorn Memorial Hospital diagnosed by imaging were retrospectively enrolled from January 2016 to December 2020. A total of 113 patients (91.9%) had Child A cirrhosis with a median model for end-stage liver disease (MELD) score of less than 9. Baseline clinical and laboratory variables and decompensation events were collected. The ALBI score was calculated and validated to classify decompensation risk into low-, middle-, and high-risk groups using three ALBI grade ranges (ALBI grade 1: ≤ -2.60; grade 2: > -2.60 but ≤ -1.39; grade 3: > -1.39). Decompensation events were defined as ascites development, variceal bleeding, or grade 3 or 4 hepatic encephalopathy.
Among 123 cirrhotic patients enrolled, 13.8% ( = 17) developed decompensating events at a median time of 25 [95% confidence interval (CI): 17-31] mo. Median baseline ALBI score in compensated cirrhosis was significantly lower than that of patients who developed decompensation events [-2.768 (-2.956 to -2.453) -2.007 (-2.533 to -1.537); = 0.01]. Analysis of decompensation risk at 3 years showed that ALBI score had a time-dependent area under the curve (tAUC) of 0.86 (95%CI: 0.78-0.92), which was significantly better than that of ALBI-Fibrosis-4 (ALBI-FIB4) score (tAUC = 0.77), MELD score (tAUC = 0.66), Child-Pugh score (tAUC = 0.65), and FIB-4 score (tAUC = 0.48) ( < 0.05 for all). The 3-year cumulative incidence of decompensation was 3.1%, 22.6%, and 50% in the low-, middle-, and high-risk groups, respectively ( < 0.001). The odds ratio for decompensation in patients of the high-risk group was 23.33 (95%CI: 3.88-140.12, = 0.001).
The ALBI score accurately identifies decompensation risk at the 3-year follow-up in patients with compensated cirrhosis. Those cirrhotic patients with a high-risk grade of ALBI score showed a 23 times greater odds of decompensation.
白蛋白-胆红素(ALBI)评分是一种最近开发的肝功能指数,用于评估肝细胞癌(HCC)患者的预后。它可以检测肝功能的微小变化,并已成功应用于各种病因的非恶性肝病患者的生存预测。
探讨 ALBI 评分在预测代偿性肝硬化患者 3 年随访时发生失代偿的风险。
回顾性纳入 2016 年 1 月至 2020 年 12 月在泰国朱拉隆功国王纪念医院通过影像学诊断为代偿性肝硬化且无 HCC 的 123 例患者。共有 113 例(91.9%)患者为 Child A 级肝硬化,中位终末期肝病模型(MELD)评分<9。收集基线临床和实验室变量以及失代偿事件。计算 ALBI 评分并验证,以三种 ALBI 分级范围(ALBI 分级 1:≤-2.60;分级 2:>-2.60 但≤-1.39;分级 3:>-1.39)将失代偿风险分类为低危、中危和高危组。失代偿事件定义为腹水形成、静脉曲张出血或 3 或 4 级肝性脑病。
在纳入的 123 例肝硬化患者中,13.8%(=17)在中位 25 [95%置信区间(CI):17-31]个月时发生失代偿事件。代偿性肝硬化患者的中位基线 ALBI 评分明显低于发生失代偿事件的患者[-2.768(-2.956 至-2.453)与-2.007(-2.533 至-1.537);=0.01]。分析 3 年的失代偿风险,ALBI 评分的时间依赖性曲线下面积(tAUC)为 0.86(95%CI:0.78-0.92),明显优于 ALBI-Fibrosis-4(ALBI-FIB4)评分(tAUC=0.77)、MELD 评分(tAUC=0.66)、Child-Pugh 评分(tAUC=0.65)和 FIB-4 评分(tAUC=0.48)(均<0.05)。低、中、高危组 3 年累积失代偿发生率分别为 3.1%、22.6%和 50%(<0.001)。高危组的失代偿比值比为 23.33(95%CI:3.88-140.12,=0.001)。
ALBI 评分可准确预测代偿性肝硬化患者 3 年随访时的失代偿风险。ALBI 评分高危级的肝硬化患者发生失代偿的可能性增加 23 倍。