Lok Anna S F, Ghany Marc G, Goodman Zachary D, Wright Elizabeth C, Everson Gregory T, Sterling Richard K, Everhart James E, Lindsay Karen L, Bonkovsky Herbert L, Di Bisceglie Adrian M, Lee William M, Morgan Timothy R, Dienstag Jules L, Morishima Chihiro
Division of Gastroenterology, University of Michigan Medical Center, 3912 Taubman Center, Ann Arbor, MI 48210, USA.
Hepatology. 2005 Aug;42(2):282-92. doi: 10.1002/hep.20772.
Knowledge of the presence of cirrhosis is important for the management of patients with chronic hepatitis C (CHC). Most models for predicting cirrhosis were derived from small numbers of patients and included subjective variables or laboratory tests that are not readily available. The aim of this study was to develop a predictive model of cirrhosis in patients with CHC based on standard laboratory tests. Data from 1,141 CHC patients including 429 with cirrhosis were analyzed. All biopsies were read by a panel of pathologists (blinded to clinical features), and fibrosis stage was determined by consensus. The cohort was divided into a training set (n = 783) and a validation set (n = 358). Variables that were significantly different between patients with and without cirrhosis in univariate analysis were entered into logistic regression models, and the performance of each model was compared. The area under the receiver-operating characteristic curve of the final model comprising platelet count, AST/ALT ratio, and INR in the training and validation sets was 0.78 and 0.81, respectively. A cutoff of less than 0.2 to exclude cirrhosis would misclassify only 7.8% of patients with cirrhosis, while a cutoff of greater than 0.5 to confirm cirrhosis would misclassify 14.8% of patients without cirrhosis. The model performed equally well in fragmented and nonfragmented biopsies and in biopsies of varying lengths. Use of this model might obviate the requirement for a liver biopsy in 50% of patients with CHC. In conclusion, a model based on standard laboratory test results can be used to predict histological cirrhosis with a high degree of accuracy in 50% of patients with CHC.
了解肝硬化的存在对于慢性丙型肝炎(CHC)患者的管理至关重要。大多数预测肝硬化的模型来自少数患者,并且包含主观变量或不易获得的实验室检查。本研究的目的是基于标准实验室检查开发一种CHC患者肝硬化的预测模型。分析了1141例CHC患者的数据,其中包括429例肝硬化患者。所有活检标本由一组病理学家阅读(对临床特征不知情),并通过共识确定纤维化阶段。该队列分为训练集(n = 783)和验证集(n = 358)。将单变量分析中肝硬化患者和无肝硬化患者之间有显著差异的变量纳入逻辑回归模型,并比较每个模型的性能。最终模型包括血小板计数、AST/ALT比值和INR,其在训练集和验证集中的受试者操作特征曲线下面积分别为0.78和0.81。小于0.2的截断值排除肝硬化仅会将7.8%的肝硬化患者误分类,而大于0.5的截断值确认肝硬化会将14.8%的无肝硬化患者误分类。该模型在碎片化和非碎片化活检以及不同长度的活检中表现同样良好。使用该模型可能使50%的CHC患者无需进行肝活检。总之,基于标准实验室检查结果的模型可用于在50%的CHC患者中高度准确地预测组织学肝硬化。