影响接受富马酸替诺福韦二吡呋酯治疗的慢性乙型肝炎患者HBV DNA抑制的因素。
Factors affecting HBV DNA suppression in chronic hepatitis B patients treated with tenofovir disoproxil fumarate.
作者信息
Darmadi Darmadi, Lindarto Dharma, Siregar Jelita, Widyawati Tri, Rusda Muhammad, Amin Mustafa Mahmud, Yusuf Fauzi, Eyanoer Putri Chairani, Lubis Masrul, Rey Imelda
机构信息
Department of Internal Medicine, Faculty of Medicine, Universitas Sumatera Utara, Medan, North Sumatera, 20155, Indonesia.
Philosophy Doctor in Medicine Program, Faculty of Medicine, Universitas Sumatera Utara, Medan, North Sumatera, 20155, Indonesia.
出版信息
F1000Res. 2023 Aug 24;11:1521. doi: 10.12688/f1000research.128116.2. eCollection 2022.
This study aims to determine the factors affecting HBV DNA suppression in chronic hepatitis B patients with tenofovir disoproxil fumarate (TDF). A case-control was carried out from October 2021 to August 2022 on 182 chronic hepatitis B patients who had TDF therapy regularly for 24 weeks at H. Adam Malik and USU Hospitals in Medan, Indonesia. The history of the samples was obtained, followed by physical examination, and blood collection. CTLA-4 polymorphism examination was carried out using real-time PCR, while the serum CTLA-4 levels were assessed with ELISA. The CTLA-4 -1661G>A polymorphism, genotype GG+AG, increased 1.52 times risk of not achieving HBV DNA suppression to TDF compared to genotype AA (p=0.041). High CTLA-4 levels increased 2.28 times risk, high HBV DNA levels increased 2.09 times risk, low ALT levels increased 1.95 times risk of not achieving HBV DNA suppression (p= 0.009, 0.026, 0.036, respectively). There was no relationship between gender, age, ethnicity, obesity, baseline AST, HBeAg, genotype, liver fibrosis and HBV DNA suppression after 24 weeks of treatment (p>0.05). The levels of CTLA-4, HBV DNA, ALT, and CTLA-4 -1661G>A polymorphism have a potential relationship with the suppression of HBV DNA in chronic hepatitis B patients with TDF.
本研究旨在确定影响慢性乙型肝炎患者使用替诺福韦酯(TDF)后HBV DNA抑制的因素。2021年10月至2022年8月,在印度尼西亚棉兰的H. Adam Malik医院和苏门答腊大学医院,对182例接受TDF正规治疗24周的慢性乙型肝炎患者进行了病例对照研究。获取样本病史,随后进行体格检查和采血。使用实时PCR进行CTLA-4基因多态性检测,同时采用ELISA法评估血清CTLA-4水平。与AA基因型相比,CTLA-4 -1661G>A基因多态性、GG+AG基因型患者未实现TDF对HBV DNA抑制的风险增加1.52倍(p=0.041)。高CTLA-4水平使风险增加2.28倍,高HBV DNA水平使风险增加2.09倍,低ALT水平使未实现HBV DNA抑制的风险增加1.95倍(p分别为0.009、0.026、0.036)。治疗24周后,性别、年龄、种族、肥胖、基线AST、HBeAg、基因型、肝纤维化与HBV DNA抑制之间无相关性(p>0.05)。CTLA-4水平、HBV DNA水平、ALT水平以及CTLA-4 -1661G>A基因多态性与慢性乙型肝炎患者使用TDF后HBV DNA的抑制存在潜在关联。