HBeAg Negativity Is Associated With More Advanced Liver Fibrosis in Patients With Chronic Hepatitis B A Propensity Score-Matching Analysis

被引:4
作者
Wang, Jian [1 ]
Wu, Weihua [1 ]
Yan, Xiaomin [1 ]
Wei, Jie [3 ]
Yao, Kefang [3 ]
Yang, Yue [1 ]
Xiong, Yali [1 ]
Xia, Juan [1 ]
Liu, Yong [2 ]
Chen, Yuxin [2 ]
Jia, Bei [1 ]
Zhang, Zhaoping [1 ]
Ding, Weimao [4 ]
Huang, Rui [1 ]
Wu, Chao [1 ]
机构
[1] Nanjing Univ, Affiliated Hosp, Nanjing Drum Tower Hosp, Dept Infect Dis,Med Sch, 321 Zhongshan Rd, Nanjing 210008, Jiangsu, Peoples R China
[2] Nanjing Univ, Affiliated Hosp, Nanjing Drum Tower Hosp, Dept Lab Med,Med Sch, Nanjing, Peoples R China
[3] Nanjing Med Univ, Dept Infect Dis, Nanjing Drum Tower Hosp, Clin Coll, Nanjing, Peoples R China
[4] Huaian 4 Peoples Hosp, Dept Hepatol, Huaian, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
chronic hepatitis B; liver fibrosis; HBeAg; propensity score matching; CORE PROMOTER; HEPATOCELLULAR-CARCINOMA; VIRAL LOAD; VIRUS; MUTATIONS; RISK; GUIDELINES; MANAGEMENT; FRANCE;
D O I
10.1097/MCG.0000000000001291
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Serum hepatitis B e antigen (HBeAg) status is associated with the progression of chronic hepatitis B (CHB). The authors aimed to investigate the relationship between HBeAg status and liver pathology in CHB patients. Methods: A total of 683 treatment-naive CHB patients who had undergone liver biopsy were retrospectively enrolled from 2 medical centers. Propensity score-matching (PSM) method was performed to adjust the imbalance of baseline confounders between HBeAg-positive and HBeAg-negative CHB patients. Results: HBeAg-negative CHB patients (n=338) exhibited more advanced liver fibrosis than HBeAg-positive CHB patients (n=345) before PSM (P<0.001). However, there were no significant differences in the distribution of inflammation grades between HBeAg-positive and HBeAg-negative CHB patients (P=0.051). Of these 683 CHB patients, 123 patients were included in each group after PSM. HBeAg-negative CHB patients still showed significantly advanced liver fibrosis as compared with HBeAg-positive CHB patients (P=0.03) after PSM. Furthermore, the distribution of liver inflammation grades in the HBeAg-negative CHB patients was also more severe than patients with HBeAg-positive (P=0.037). HBeAg-negative status was identified as an independent risk factor of significant liver fibrosis (P=0.011) by multivariate analysis. Conclusions: HBeAg negativity is associated with more advanced liver fibrosis in CHB patients.
引用
收藏
页码:826 / 831
页数:6
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