Impact of Non‐Alcoholic Fatty Liver Disease on the HBsAg Loss of Patients With Chronic Hepatitis B Treated in Pegylated Interferon Alpha

医学 乙型肝炎表面抗原 内科学 胃肠病学 聚乙二醇干扰素 脂肪肝 乙型肝炎 回顾性队列研究 肝病 人口 慢性肝炎 非酒精性脂肪肝 减肥 队列 肝病学 队列研究 联合疗法 倾向得分匹配 慢性肝病 丙型肝炎 乙型肝炎病毒 前瞻性队列研究 人口研究 疾病 α-干扰素 免疫学
作者
Chujing Li,Lihua Lin,Pei Zhou,Haiyi Cai,Songlian Liu,Xiaoyuan Chen,Aiqi Lu,Bo Li,Yaping Wang,Chuanghua Luo,Jianping Li,Yujuan Guan,Zhiwei Xie
出处
期刊:Journal of Viral Hepatitis [Wiley]
卷期号:33 (1): e70115-e70115
标识
DOI:10.1111/jvh.70115
摘要

Whether combining non-alcoholic fatty liver disease (NAFLD) affects the efficacy of pegylated interferon alpha (PEG-IFN-α) for patients with chronic hepatitis B (CHB) remains unknown; hence, we aimed to conduct a retrospective cohort study to investigate the impact of NAFLD on the HBsAg loss rate of CHB treated with PEG-IFN-α. A total of 279 adult CHB patients receiving antiviral therapy with PEG-IFN-α were included in the study, of which 94 (33.7%) patients had combined NAFLD. The median treatment duration in the overall population was 37 (23, 59) weeks, and 79 (28.3%) patients achieved serum HBsAg loss during treatment. Compared to patients without NAFLD, patients with NAFLD had lower baseline HBsAg levels prior to treatment with PEG-IFN-α (438.05 [152.77, 978.60] vs. 296.60 [54.20, 647.15] IU/mL, p = 0.004). Propensity score matching (PSM) was applied to rectify the baseline characteristics between the two groups, including age, gender and quantitative HBsAg level. After PSM, 84 CHB with NAFLD and 84 CHB without NAFLD were included in the matched cohort. With a comparable treatment duration in both groups, the patients with NAFLD had a lower cumulative HBsAg loss rate (Log-rank p = 0.007). Multivariable analysis suggested that NAFLD was independently associated with a decrease in HBsAg loss rates (risk ratio HR = 0.505; 95% CI, 0.283-0.902; p = 0.021), which was consistent in sensitivity analyses that included only nucleos(t)ide analogue (NA)-treated patients. In conclusion, CHB with NAFLD demonstrated a lower HBsAg loss rate during PEG-IFN-α treatment, suggesting that more optimal therapeutic strategies need to be further explored.
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