前药。 2022; 13:824879。 EPUB 2022 FEB 2.PMID: 35185575 Sanduzzi-Zamparelli, Victor Sapena, Maria Guarino, Marcello Dallio, Emanuele Torrisi, Luca Pignata, Alessandro Federico, Federico Salomone, Filomena Morisco
Article Affiliation:Valentina Cossiga
Abstract:HCV eradication by direct-acting antivirals (DAAs) improves liver结果并降低了总体肝死亡率。然而,尽管病毒清除。 Silybin在实验模型中显示出肝保护作用,但临床数据受到限制。 The aim of this study is to evaluate the effect of a highly bioavailable form of silybin on liver fibrosis in patients with HCV-related ACLD after viral eradication with DAAs, in comparison with the standard of care.In this multicenter and prospective study, HCV patients with ACLD achieving SVR12 were treated with the combination of silybinphospholipid complex with vitamin D and vitamin E (Realsil 100d,Ibi Lorenzini S.P.A.,意大利Aprilia,意大利Aprilia)持续了12个月(R组),与对照组(C组)相比。在基线,第24周和第48周将患者提交瞬时弹性图(TE)和增强的肝纤维化(ELF)测试。招募了100名6名患者,R组为56例,C组60例。中位年龄为68岁,男性为53%,两组之间没有差异。在这两组中,与基线相比,肝脏刚度在6和12个月时提高。然而,与C组的患者相比,R组的患者在6个月后(-2.05,95%CI -3.89至-0.22,<0.05)和12个月的治疗(-2.79,95%CI -4.5至-1.09,<0.01)在6个月后的肝脏刚度降低较高。两组之间没有观察到小精灵还原的显着差异。在随访期间,四名患者都在C组中发展了HCC。在与HCV相关的ACLD中,甲硅烷基蛋白的肝保护作用可能代表了抵消肝病进展的工具。