Abstract
Introduction: chronic hepatitis B (CHB) is a serious and common infectious disease, the pathogenesis of which has not been fully elucidated. Tenofovir Amibufenamide belongs to the nucleoside reverse transcriptase inhibitor class and was allowed for CHB treatment. This work investigated the effectiveness and safety of Tenofovir Amibufenamide in treating HBeAg-positive CHB. Materials and Methods: 60 patients with HBeAg-positive CHB were grouped: an entecavir (ETV) group (entecavir, 0.5 mg) and a TMF group (Tenofovir Amibufenamide, 0.25 mg) at a 1:1 ratio. Changes in renal function, liver function, and tumor necrosis factor α (TNF-α) levels after 2 years of treatment were analyzed to assess the antiviral efficacy and safety. Results: patients in TMF group showed smaller changes in serum creatinine (Scr) and glomerular filtration rate (GFR) after treatment, and decreased alanine aminotransferase (ALT) and total bilirubin (TBIL), demonstrating obvious differences with those in ETV group (P<0.05). Postoperative TNF-α was elevated greatly in ETV group, showing obvious difference with that in TMF group (P<0.05). Meanwhile, in contrast to the ETV group, patients in the TMF group presented lower hepatitis B surface antigen (HBsAg), hepatitis B e antigen (HBeAg), and hepatitis B DNA load after treatment (P<0.05). Furthermore, the post-treatment incidence of adverse reactions (IoAR) was 13.3% in the ETV group and 3.3% in the TMF group (P>0.05). Conclusion: Tenofovir Amibufenamide in treating HBeAg-positive CHB exhibited better efficacy, remarkable improvement in liver function, no impact on renal function, and high safety.
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