Prediction of significant fibrosis in HBeAg-positive patients with chronic hepatitis B by a noninvasive model

医学 内科学 胃肠病学 切断 接收机工作特性 HBeAg 纤维化 肝活检 乙型肝炎 预测值 慢性肝炎 肝纤维化 乙型肝炎病毒 活检 乙型肝炎表面抗原 免疫学 病毒 物理 量子力学
作者
Minde Zeng,Lungen Lu,Yimin Mao,Dekai Qiu,Jiqiang Li,Mobin Wan,Chengwei Chen,Jiyao Wang,Xiong Cai,Chunfang Gao,Xia-qiu Zhou
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:42 (6): 1437-1445 被引量:157
标识
DOI:10.1002/hep.20960
摘要

A model was constructed consisting of clinical and serum variables to discriminate between hepatitis B e antigen (HBeAg)-positive chronic hepatitis B (CHB) patients with and without significant fibrosis (stages 2-4 vs. stages 0-1). Consecutive treatment-naive CHB patients who underwent liver biopsy were divided into 2 sequential groups: a training group (n = 200) and a validation group (n = 172). Multivariate analysis identified α2-macroglobulin, age, gamma glutamyl transpeptidase, and hyaluronic acid as independent predictors of fibrosis. The area under the receiver operating characteristic curve was 0.84 for the training group and 0.77 for the validation group. Using a cutoff score of <3.0, the presence of significant fibrosis (F2 to F4) could be excluded with high accuracy (86.1% negative predictive value [NPV], 70.1% positive predictive value [PPV], and 94.8% sensitivity) in 43 (21.5%) of 200 patients in the training group, and with the same certainty (90.9% NPV, 64.7% PPV, and 98.0% sensitivity) in 22 (12.8%) of 172 patients in the validation group. Similarly, applying a cutoff score of >8.7, the presence of significant fibrosis could be correctly identified with high accuracy (91.1% PPV, 51.6% NPV, and 95.2% specificity) in 41 (20.5%) of 200 patients in the training group, and with the same certainty (84.8% PPV, 52.4% NPV, and 90.4% specificity) in 39 (22.7%) of 172 patients of the validation group. In conclusion, a predictive model with a combination of easily accessible variables identified HBeAg-positive CHB patients with and without significant fibrosis with a high degree of accuracy. Application of this model may decrease the need for liver biopsy in staging of 35.5% CHB. (HEPATOLOGY 2005;42:1437–1445.)
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