Su Changtian, Yang Qin
Department of Liver Disease, Sichuan Leshan Traditional Chinese Medicine Hospital, Leshan, China.
Front Pharmacol. 2022 Dec 14;13:1032789. doi: 10.3389/fphar.2022.1032789. eCollection 2022.
This study aims to investigate the clinical efficacy of Ganshuang granules combined with tenofovir, an antiviral drug, in the treatment of chronic hepatitis B complicated with nonalcoholic fatty liver disease. A total of 92 patients with chronic hepatitis B combined with non-alcoholic fatty liver who were treated in our Hospital from January 2020 to December 2021 were included as the research objects. According to the method of random number table, the patients were divided into the control group ( = 42) and the treatment group ( = 50). The control group was treated with silibinin meglumine tablets and tenofovir, while the treatment group was treated with Ganshuang granules combined with silybin meglumine tablets and tenofovir. Before and after treatment, liver function index, liver hardness measurement (LSM), controlled attenuation parameter (CAP), HBV-DNA serum load and body mass index (BMI) were observed. Compared with the baseline, ALT, AST and GGT were significantly improved in both groups after treatment ( < 0.05), while TBIL indexes were not significantly different before and after treatment ( > 0.05). Patients in the treatment group had significantly lower ALT and AST index values than the control group at 12 and 24 weeks of treatment ( < 0.05). At 12 and 24 weeks of treatment, the fat attenuation parameters of the two groups were significantly decreased compared with those before treatment, and the difference was statistically significant ( < 0.05). The fat attenuation parameters in the treatment group were significantly lower than those in the control group at 12 and 24 weeks after treatment ( < 0.05). The effect of Ganshuang granule combined with antiviral drugs in the treatment of chronic hepatitis B complicated with non-alcoholic fatty liver is significantly better than that of antiviral drugs alone, which is worthy of clinical recommendation. https://register.clinicaltrials.gov, identifier NCT05523648.
本研究旨在探讨肝爽颗粒联合抗病毒药物替诺福韦治疗慢性乙型肝炎合并非酒精性脂肪性肝病的临床疗效。选取2020年1月至2021年12月在我院治疗的92例慢性乙型肝炎合并非酒精性脂肪性肝病患者作为研究对象。根据随机数字表法,将患者分为对照组( = 42)和治疗组( = 50)。对照组给予水飞蓟宾葡甲胺片和替诺福韦治疗,治疗组给予肝爽颗粒联合水飞蓟宾葡甲胺片和替诺福韦治疗。观察治疗前后的肝功能指标、肝脏硬度值(LSM)、受控衰减参数(CAP)、HBV-DNA血清载量及体重指数(BMI)。与基线相比,两组治疗后ALT、AST和GGT均显著改善( < 0.05),而TBIL指标治疗前后差异无统计学意义( > 0.05)。治疗组在治疗12周和24周时ALT和AST指标值显著低于对照组( < 0.05)。治疗12周和24周时,两组脂肪衰减参数均较治疗前显著降低,差异有统计学意义( < 0.05)。治疗组治疗后12周和24周时脂肪衰减参数显著低于对照组( < 0.05)。肝爽颗粒联合抗病毒药物治疗慢性乙型肝炎合并非酒精性脂肪性肝病的效果明显优于单纯抗病毒药物,值得临床推荐。https://register.clinicaltrials.gov,标识符NCT05523648 。