The Relationship between Viral Replication and the Severity of Hepatic Necroinflammatory Damage Changed before HBeAg Loss in Patients with Chronic Hepatitis B Virus Infection

被引:1
|
作者
Wang, Leijie [1 ,2 ,3 ]
Wang, Jian [4 ]
Zhao, Kunyu [1 ]
Jiang, Lina [5 ]
Zhang, Xinxin [6 ]
Zhao, Jingming [5 ]
Li, Jie [4 ]
Lu, Fengmin [2 ,3 ]
机构
[1] Zhengzhou Univ, Coll Basic Med Sci, Dept Microbiol & Immunol, Zhengzhou, Henan, Peoples R China
[2] Peking Univ, Sch Basic Med Sci, Dept Microbiol, 38 Xueyuan Rd, Beijing 100191, Peoples R China
[3] Peking Univ, Infect Dis Ctr, Sch Basic Med Sci, 38 Xueyuan Rd, Beijing 100191, Peoples R China
[4] Nanjing Univ, Nanjing Drum Tower Hosp, Affiliated Hosp, Dept Infect Dis,Med Sch, Nanjing 210000, Jiangsu, Peoples R China
[5] Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Pathol & Hepatol, Beijing, Peoples R China
[6] Shanghai Jiao Tong Univ, Sch Med, Rui Jin Hosp, Dept Infect Dis, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Chronic hepatitis B; HBeAg; HBV DNA; ALT; E-ANTIGEN; SURFACE-ANTIGEN; LIVER-DISEASE; CHILDREN; DNA;
D O I
10.14218/JCTH.2023.00378
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Disease progression of chronic hepatitis B virus (HBV) infection is driven by the interactions between viral replication and the host immune response against the infection. This study aimed to clarify the relationship between HBV replication and hepatic inflammation during disease progression. Methods: Two cross-sectional, one validation cohort, and meta-analyses were used to explore the relationship between HBV replication and liver inflammation. Spearman analysis, multiple linear regression, and logistic regression were used to explore the relationship between variables.Results: In the cross-sectional cohorts A and B including 1,350 chronic hepatitis B patients, Spearman analysis revealed a negative relationship between HBV replication (such as HBV DNA) and liver inflammation (such as ALT) in HBeAg-positive patients with higher HBV DNA >2x10(6) IU/mL (rho=-0.160 and -0.042) which turned to be positive in HBeAg-positive patients with HBV DNA <= 2x10(6) IU/mL (rho=0.278 and 0.260) and HBeAg-negative patients (rho=0.450 and 0.363). After adjustment for sex, age, and anti-HBe, results from logistic regression and multiple linear regression showed the opposite relationship still existed in HBeAg-positive patients with different DNA levels; the opposite relationship in HBeAg-positive patients with different DNA levels was validated in a third cohort; the opposite relationship in patients with different HBeAg status was partially confirmed by meta-analysis (overall R: -0.004 vs 0.481).Conclusions: These results suggested a negative relationship between viral replication and liver inflammation in HBeAg-positive patients with high HBV DNA, which changed to a positive relationship for those HBeAg-positive patients with DNA less than 2x10(6) IU/mL and HBeAg-negative patients.
引用
收藏
页码:381 / 388
页数:8
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