Liver Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Barcelona, Spain.
Hepatology. 2012 Jun;55(6):1931-41. doi: 10.1002/hep.25614. Epub 2012 Apr 23.
Alcoholic hepatitis (AH) is a severe condition developed in patients with underlying alcoholic liver disease. Ductular reaction has been associated with chronic alcohol consumption but there is no information regarding the extent of liver progenitor cell (LPC) proliferation in AH. The aim of this study was to investigate LPC markers in AH and its correlation with disease severity. Fifty-nine patients with clinical and histological diagnosis of AH were included in the study. LPC markers were assessed by real-time polymerase chain reaction (PCR) and immunohistochemistry. Standard logistic regression analysis and classification and regression trees (CART) analysis were used for statistical analysis. A microarray analysis showed an up-regulation of LPC markers in patients with AH. Real-time PCR demonstrated that epithelial cell adhesion molecule (EpCAM), Prominin-1, and Keratin7 were significantly increased in patients with AH compared with normal livers (P ≤ 0.01), chronic hepatitis C (P ≤ 0.01), and HCV-induced cirrhosis (P ≤ 0.01). Immunohistochemistry scores generated for Keratin7 and EpCAM demonstrated a good correlation with gene expression. Keratin7 gene expression correlated with liver failure as assessed by model for endstage liver disease score (r = 0.41, P = 0.006) and Maddrey's discriminant function (r = 0.43, P = 0.004). Moreover, Keratin7 (OR1.14, P = 0.004) and Prominin-1 (OR1.14, P = 0.002), but not EpCAM (OR1.16, P = 0.06), were identified as independent predictors of 90-day mortality. CART analysis generated an algorithm based on the combination of Keratin7 and EpCAM gene expression that stratified three groups of patients with high, intermediate, and low short-term mortality (89%, 33%, and 6%, respectively; area under the receiver operating curve 0.73, 95% confidence interval 0.60-0.87). Keratin7 expression provided additional discrimination potential to the age, bilirubin, international normalization ratio, creatinine (ABIC) score.
LPC markers correlate positively with severity of liver disease and short-term mortality in AH patients. This study suggests that LPC proliferation may be an important feature of AH pathophysiology.
酒精性肝炎(AH)是在患有基础酒精性肝病的患者中发展的一种严重病症。胆管反应与慢性酒精消耗有关,但尚无关于 AH 中肝祖细胞(LPC)增殖程度的信息。本研究旨在研究 AH 中的 LPC 标志物及其与疾病严重程度的关系。将 59 例临床和组织学诊断为 AH 的患者纳入研究。通过实时聚合酶链反应(PCR)和免疫组织化学评估 LPC 标志物。标准逻辑回归分析和分类回归树(CART)分析用于统计分析。微阵列分析显示,AH 患者的 LPC 标志物上调。实时 PCR 显示,与正常肝脏(P≤0.01)、慢性丙型肝炎(P≤0.01)和 HCV 诱导的肝硬化(P≤0.01)相比,上皮细胞黏附分子(EpCAM)、Prominin-1 和角蛋白 7 在 AH 患者中显着增加。免疫组织化学评分显示,角蛋白 7 和 EpCAM 的基因表达具有良好的相关性。角蛋白 7 基因表达与终末期肝病模型评分(r=0.41,P=0.006)和 Maddrey 判别函数(r=0.43,P=0.004)评估的肝功能衰竭相关。此外,角蛋白 7(OR1.14,P=0.004)和 Prominin-1(OR1.14,P=0.002),而不是 EpCAM(OR1.16,P=0.06),被确定为 90 天死亡率的独立预测因子。CART 分析生成了一种基于角蛋白 7 和 EpCAM 基因表达组合的算法,该算法将高、中、低短期死亡率的三组患者分层(分别为 89%、33%和 6%;接受者操作特征曲线下面积为 0.73,95%置信区间为 0.60-0.87)。角蛋白 7 表达为 ABIC 评分提供了年龄、胆红素、国际标准化比值、肌酐(ABIC)评分的额外鉴别潜力。
LPC 标志物与 AH 患者肝病严重程度和短期死亡率呈正相关。本研究表明,LPC 增殖可能是 AH 病理生理学的一个重要特征。