富马酸替诺福韦酯改用替诺福韦阿拉非那胺三年后肝纤维化得到改善

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Tung Huynh, Delana MyAn Bui, Tina Xiwen Zhou, Ke-Qin Hu
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引用次数: 0

摘要

背景 Tenofovir alafenamide(TAF)和富马酸替诺福韦二吡呋酯(TDF)都是慢性乙型肝炎(CHB)的一线治疗药物。我们的研究表明,从 TDF 转为 TAF 治疗 96 周后,丙氨酸氨基转移酶(ALT)进一步改善,但仍缺乏 TDF 转为 TAF 对肝纤维化的长期益处的数据。目的 评估TDF改用TAF治疗3年对CHB患者谷丙转氨酶、天冬氨酸氨基转移酶(AST)和肝纤维化改善的益处。方法 对53名最初接受TDF治疗、后转为TAF治疗的CHB患者进行单中心回顾性研究,以确定转药第144周时ALT、AST、AST与血小板比值指数(APRI)、肝纤维化-4(FIB-4)评分和剪切波弹性成像(SWE)读数改善的动态模式及其相关因素。结果 平均年龄 55 岁(28-80 岁);45.3% 为男性;15.1% 为临床肝硬化;平均基线谷丙转氨酶(ALT)24.8;谷草转氨酶(AST)25.7 U/L;APRI 0.37;FIB-4 1.66。TDF 转为 TAF 144 周后,平均 ALT 和 AST 分别降至 19.7 和 21。从基线到换药第144周,ALT和AST<35(男)/25(女)和<30(男)/19(女)的比率持续上升;肝纤维化也因APRI<0.5,分别从79.2%降至96.2%;FIB-4<1.45,分别从52.8%降至58.5%;平均APRI降至0.27;FIB-4降至1.38;平均SWE读数在平均109周转换后从7.05降至6.30 kPa。肾功能稳定,肾小球滤过率大于 60 毫升/分钟的患者从基线时的 86.5%增加到换药第 144 周时的 88.2%。结论 我们的数据证实,从 TDF 转为 TAF 治疗 3 年,不仅能持续改善 ALT/AST,还能通过 APRI、FIB-4 评分以及 SWE 读数改善肝纤维化,这是 TAF 长期乙肝病毒抗病毒治疗的重要临床益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improvement of hepatic fibrosis after tenofovir disoproxil fumarate switching to tenofovir alafenamide for three years
BACKGROUND Both tenofovir alafenamide (TAF) and tenofovir disoproxil fumarate (TDF) are the first-line treatments for chronic hepatitis B (CHB). We have showed switching from TDF to TAF for 96 weeks resulted in further alanine aminotransferase (ALT) improvement, but data remain lacking on the long-term benefits of TDF switching to TAF on hepatic fibrosis. AIM To assess the benefits of TDF switching to TAF for 3 years on ALT, aspartate aminotransferase (AST), and hepatic fibrosis improvement in patients with CHB. METHODS A single center retrospective study on 53 patients with CHB who were initially treated with TDF, then switched to TAF to determine dynamic patterns of ALT, AST, AST to platelet ratio index (APRI), fibrosis-4 (FIB-4) scores, and shear wave elastography (SWE) reading improvement at switching week 144, and the associated factors. RESULTS The mean age was 55 (28-80); 45.3%, males; 15.1%, clinical cirrhosis; mean baseline ALT, 24.8; AST, 25.7 U/L; APRI, 0.37; and FIB-4, 1.66. After 144 weeks TDF switching to TAF, mean ALT and AST were reduced to 19.7 and 21, respectively. From baseline to switching week 144, the rates of ALT and AST < 35 (male)/25 (female) and < 30 (male)/19 (female) were persistently increased; hepatic fibrosis was also improved by APRI < 0.5, from 79.2% to 96.2%; FIB-4 < 1.45, from 52.8% to 58.5%, respectively; mean APRI was reduced to 0.27; FIB-4, to 1.38; and mean SWE reading, from 7.05 to 6.30 kPa after a mean of 109 weeks switching. The renal function was stable and the frequency of patients with glomerular filtration rate > 60 mL/min was increased from 86.5% at baseline to 88.2% at switching week 144. CONCLUSION Our data confirmed that switching from TDF to TAF for 3 years results in not only persistent ALT/AST improvement, but also hepatic fibrosis improvement by APRI, FIB-4 scores, as well as SWE reading, the important clinical benefits of long-term hepatitis B virus antiviral treatment with TAF.
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来源期刊
World Journal of Hepatology
World Journal of Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.10
自引率
4.20%
发文量
172
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