Improvement of hepatic fibrosis after tenofovir disoproxil fumarate switching to tenofovir alafenamide for three years

被引:1
|
作者
Huynh, Tung [1 ]
Bui, Delana MyAn [2 ]
Zhou, Tina Xiwen [3 ]
Hu, Ke-Qin [4 ]
机构
[1] Univ Calif Orange, Dept Pharm, Irvine Med Ctr, Orange, CA 92868 USA
[2] Univ Houston, Houston, TX 77204 USA
[3] Rosalind Franklin Univ, Chicago Med Sch, N Chicago, IL 60064 USA
[4] Univ Calif Irvine, Sch Med, Div Gastroenterol & Hepatol, 101 The City Dr,Bldg 22C,Room 1503,, Orange, CA 92868 USA
关键词
Tenofovir alafenamide; Tenofovir disoproxil fumarate; Switching; Hepatic fibrosis improvement; Aspartate aminotransferase to platelet ratio index; Fibrosis-4; Shear wave elastography; TRANSIENT ELASTOGRAPHY; LIVER FIBROSIS; APRI;
D O I
10.4254/wjh.v16.i7.1009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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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