Zhang Chenxia, Chen Xinyue, Hong Zehua, Qi Yan, Wang Xudong, Dai Yaping, Qiu Yuanwang
Wuxi School of Medicine, Jiangnan University, Wuxi, Jiangsu, China.
Department of Infectious Diseases, Affiliated Wuxi Fifth Hospital of Jiangnan University, Wuxi, Jiangsu, China.
Medicine (Baltimore). 2025 Aug 29;104(35):e43946. doi: 10.1097/MD.0000000000043946.
Nucleos(t)ide analogues (NAs) have demonstrated potent efficacy in suppressing viral replication in chronic hepatitis B (CHB). This 48-week study compared the efficacy and safety of NA treatment for CHB patients with high viral load (hepatitis B virus [HBV] deoxyribonucleic acid [DNA] > 7 log10 IU/mL). This retrospective study included 180 nucleos(t)ide-naïve CHB patients with high viral load undergoing NA monotherapy, which were stratified into 3 groups: entecavir (ETV, n = 82), tenofovir disoproxil fumarate (TDF, n = 58), and tenofovir alafenamide fumarate (TAF, n = 40). The primary endpoint was the proportion of patients achieving HBV DNA < 20 IU/mL, with safety assessed by lipid profiles and renal function. The study subjects' mean baseline HBV DNA levels were 7.68, 7.73, and 7.75 log10 IU/mL in ETV, TDF, and TAF groups, respectively. At week 48, TDF had a higher viral suppression (HBV DNA < 20 IU/mL) rate (67.74%) than TAF (37.50%) cohort (P = .004) and ETV (54.88%) was comparable to both (P > .05). Hepatitis B e antigen loss and seroconversion were comparable across all groups, with no hepatitis B surface antigen loss observed. Similar proportions of patients with high alanine aminotransferase levels at baseline achieved normalization by week 48 in all regimens. Low-density lipoprotein, total cholesterol, and triglyceride elevations were comparable across all groups. High-density lipoprotein reductions were 15.63%, 35.71%, and 17.86% in ETV, TDF, and TAF, respectively (P = .043), with TDF reducing high-density lipoprotein and total cholesterol more than ETV (P = .014 and P < .001). No significant differences were found in serum creatinine elevation or estimated glomerular filtration rates reduction among the groups. TDF was preferentially recommended for high viral load CHB patients, as its superior antiviral efficacy and comparable safety profile.
核苷(酸)类似物(NAs)已被证明在抑制慢性乙型肝炎(CHB)病毒复制方面具有强大功效。这项为期48周的研究比较了核苷(酸)类似物治疗高病毒载量(乙肝病毒[HBV]脱氧核糖核酸[DNA]>7 log10 IU/mL)CHB患者的疗效和安全性。这项回顾性研究纳入了180例接受核苷(酸)类似物单药治疗的初治高病毒载量CHB患者,这些患者被分为3组:恩替卡韦(ETV,n = 82)、富马酸替诺福韦二吡呋酯(TDF,n = 58)和富马酸丙酚替诺福韦(TAF,n = 40)。主要终点是实现HBV DNA<20 IU/mL的患者比例,通过血脂和肾功能评估安全性。ETV、TDF和TAF组研究对象的平均基线HBV DNA水平分别为7.68、7.73和7.75 log10 IU/mL。在第48周时,TDF的病毒抑制(HBV DNA<20 IU/mL)率(67.74%)高于TAF组(37.50%)(P = 0.004),ETV组(54.88%)与两者相当(P>0.05)。所有组的乙肝e抗原消失和血清学转换相当,未观察到乙肝表面抗原消失。在所有治疗方案中,基线时丙氨酸氨基转移酶水平高的患者在第48周时达到正常化的比例相似。所有组的低密度脂蛋白、总胆固醇和甘油三酯升高情况相当。ETV、TDF和TAF组的高密度脂蛋白降低分别为15.63%、35.71%和17.86%(P = 0.043),TDF降低高密度脂蛋白和总胆固醇的幅度大于ETV(P = 0.014和P<0.001)。各组间血清肌酐升高或估计肾小球滤过率降低无显著差异。TDF因其卓越的抗病毒疗效和相当的安全性,被优先推荐用于高病毒载量的CHB患者。