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接受恩替卡韦治疗的慢性乙型肝炎患者低水平病毒血症相关的危险因素。

Risk factors related to low-level viraemia in chronic hepatitis B patients receiving entecavir treatment.

机构信息

Senior Department of Hepatology, the Fifth Medical Center of PLA General Hospital, Beijing, China.

Department II of Infectious Diseases (Hepatology), The Second People's Hospital of Jingzhou City, Jingzhou, China.

出版信息

Front Cell Infect Microbiol. 2024 Aug 7;14:1413589. doi: 10.3389/fcimb.2024.1413589. eCollection 2024.

Abstract

BACKGROUND

About 20% of on-treatment patients with chronic hepatitis B (CHB) experienced low-level viraemia (LLV), which is associated with persistent low-grade inflammation, fibrosis progression, and increased risk of hepatocellular carcinoma. We aimed to investigate the high-risk factors related to LLV.

METHODS

In this retrospective study, patients receiving entecavir (ETV) treatment from January 2018 to January 2023 were enrolled, and were divided into a LLV (HBV DNA 20-2000 IU/mL) cohort and a complete virological response (CVR) (HBV DNA < 20 IU/mL) cohort according to the virological response at week 48 posttreatment. Treatment baseline characteristics were retrieved from electronic medical records. Multivariate logistic regression was performed.

RESULTS

Totally, 1653 patients were enrolled, male patients accounted for 73.0%; the median age was 44 years; the mean HBV DNA level was 5.9 Log IU/ml. Among them, 472 (28.6%) experienced LLV. Multivariate analysis showed that HBeAg positivity (OR = 2.650, 95% CI: 2.000-3.511, < 0.001), HBV DNA ≥ 6.0 Log IU/mL (OR = 1.370, 95% CI: 1.054-1.780, = 0.019), qHBsAg ≥ 9000 IU/mL (OR = 4.472, 95% CI: 3.410-5.866, < 0.001), cirrhosis (OR = 1.650, 95% CI: 1.234-2.207, = 0.001), LSM ≥ 13.0 kPa (OR = 1.644, 95% CI: 1.203-2.246, = 0.002), and PLT < 100×10/L (OR = 1.450, 95% CI: 1.094-1.922, = 0.010) at baseline were related to the development of LLV.

CONCLUSIONS

High HBV DNA/HBsAg quantification/LSM, low PLT, HBeAg positivity, and liver cirrhosis were high-risk factors associated with LLV in patients receiving entecavir treatment.

摘要

背景

约 20%的慢性乙型肝炎(CHB)治疗患者出现低水平病毒血症(LLV),这与持续低度炎症、纤维化进展和肝细胞癌风险增加有关。本研究旨在探讨与 LLV 相关的高危因素。

方法

这是一项回顾性研究,纳入了 2018 年 1 月至 2023 年 1 月期间接受恩替卡韦(ETV)治疗的患者,并根据治疗后 48 周的病毒学应答将患者分为 LLV(HBV DNA 20-2000 IU/ml)队列和完全病毒学应答(CVR)(HBV DNA < 20 IU/ml)队列。从电子病历中提取治疗基线特征。采用多变量逻辑回归分析。

结果

共纳入 1653 例患者,男性占 73.0%;中位年龄为 44 岁;平均 HBV DNA 水平为 5.9 Log IU/ml。其中,472 例(28.6%)出现 LLV。多变量分析显示,HBeAg 阳性(OR=2.650,95%CI:2.000-3.511,<0.001)、HBV DNA≥6.0 Log IU/ml(OR=1.370,95%CI:1.054-1.780,=0.019)、qHBsAg≥9000 IU/ml(OR=4.472,95%CI:3.410-5.866,<0.001)、肝硬化(OR=1.650,95%CI:1.234-2.207,=0.001)、LSM≥13.0 kPa(OR=1.644,95%CI:1.203-2.246,=0.002)和基线时 PLT<100×10/L(OR=1.450,95%CI:1.094-1.922,=0.010)与 LLV 的发生有关。

结论

接受恩替卡韦治疗的患者中,高 HBV DNA/ HBsAg 定量/LSM、低血小板计数、HBeAg 阳性和肝硬化是与 LLV 相关的高危因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a297/11335720/583091b6f164/fcimb-14-1413589-g001.jpg

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