Kono Masashi, Nishida Naoshi, Hagiwara Satoru, Minami Tomohiro, Chishina Hirokazu, Arizumi Tadaaki, Minaga Kosuke, Kamata Ken, Komeda Yoriaki, Sakurai Toshiharu, Takenaka Mamoru, Takita Masahiro, Yada Norihisa, Ida Hiroshi, Minami Yasunori, Ueshima Kazuomi, Watanabe Tomohiro, Kudo Masatoshi
Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Dig Dis. 2017;35(6):556-564. doi: 10.1159/000480148. Epub 2017 Oct 17.
Direct-acting antivirals (DAAs) dramatically improve the sustained virological response (SVR) of chronic hepatitis C (CHC) patients. However, continuous liver damage after SVR may be a risk of hepatocellular carcinoma (HCC). We clarified pretreatment characteristics related to sustained liver damage after SVR.
A total of 286 CHC patients were treated with an interferon-free DAA regimen. Among them, 250 patients achieved SVR for 12 weeks after the end of treatment (SVR12); these individuals were classified based on α-fetoprotein (AFP) and alanine transaminase (ALT) levels posttreatment. Baseline characteristics significantly associated with AFP >5 ng/mL and ALT level ≥20 IU/L after SVR were clarified using multivariate analyses.
Among the pretreatment factors examined, serum AFP values and the presence of fatty liver (FL) were significantly associated with abnormal AFP (p < 0.0001) and ALT levels 12 weeks after SVR12 (SVR24; p = 0.0109). For 126 patients who showed an increase in baseline AFP level, FL, fibrosis-4 (FIB-4) index, and albumin levels before treatment were related to abnormal AFP at SVR24 (p = 0.0005, 0.0232, and 0.0400 for FL, FIB-4 index, and albumin, respectively). Similarly, for 150 patients with abnormal baseline ALT levels, FL was associated with an ALT level ≥ 30 IU/L after SVR (p = 0.0430).
High FIB-4 index, low albumin level, and FL before DAA treatment were associated with a risk of sustained liver damage with AFP and ALT elevation after SVR; patients with these factors should be carefully monitored for emergence of HCC.
直接抗病毒药物(DAAs)显著提高了慢性丙型肝炎(CHC)患者的持续病毒学应答(SVR)。然而,SVR后持续的肝损伤可能是肝细胞癌(HCC)的一个风险因素。我们阐明了与SVR后持续肝损伤相关的治疗前特征。
共有286例CHC患者接受了无干扰素的DAA方案治疗。其中,250例患者在治疗结束后实现了12周的SVR(SVR12);这些个体根据治疗后的甲胎蛋白(AFP)和丙氨酸转氨酶(ALT)水平进行分类。使用多变量分析阐明了与SVR后AFP>5 ng/mL和ALT水平≥20 IU/L显著相关的基线特征。
在所检查的治疗前因素中,血清AFP值和脂肪肝(FL)的存在与SVR12后12周(SVR24)的AFP异常(p<0.0001)和ALT水平显著相关(p = 0.0109)。对于126例基线AFP水平升高的患者,治疗前的FL、纤维化-4(FIB-4)指数和白蛋白水平与SVR24时的AFP异常相关(FL、FIB-4指数和白蛋白分别为p = 0.0005、0.0232和0.0400)。同样,对于150例基线ALT水平异常的患者,FL与SVR后ALT水平≥30 IU/L相关(p = 0.0430)。
DAA治疗前高FIB-4指数、低白蛋白水平和FL与SVR后AFP和ALT升高导致的持续肝损伤风险相关;应密切监测有这些因素的患者是否出现HCC。