| Literature DB >> 30210615 |
Kosuke Takeda1, Ryuichi Noguchi1, Tadashi Namisaki1, Kei Moriya1, Takemi Akahane1, Mitsuteru Kitade1, Hideto Kawaratani1, Naotaka Shimozato1, Kosuke Kaji1, Hiroaki Takaya1, Yasuhiko Sawada1, Kenichiro Seki1, Yukihisa Fujinaga1, Yuki Tsuji1, Takuya Kubo1, Shinya Sato1, Soichiro Saikawa1, Keisuke Nakanishi1, Masanori Furukawa1, Koh Kitagawa1, Takahiro Ozutsumi1, Daisuke Kaya1, Akira Mitoro1, Tsuyoshi Mashitani1, Yasushi Okura2, Junichi Yamao2, Hitoshi Yoshiji1.
Abstract
Depression is a major reason for interferon (IFN) therapy cessation. IFN-free direct-acting antiviral (DAA) therapy for depression is not well-documented. Thus, four different IFN-free regimens were assessed in genotype-1 hepatitis C virus (HCV) patients with depression. Overall, 287 HCV genotype-1 patients who received combination therapies with IFN-free DAAs of daclatasvir/asunaprevir (DCV/ASV) (n=84), sofosbuvir/ledipasvir (SOF/LDV) (n=95), ombitasvir/paritaprevir/ritonavir (OBV/PTV/r) (n=74), and elbasvir/grazoprevir (EBR/GZR) (n=34) were included. Treatment-induced depression as a complication of HCV therapy in IFN-free DAA regimens was assessed. The severity of depression was evaluated using the Beck Depression Inventory-II (BDI-II) questionnaire. It was demonstrated that all four DAA regimens achieved similar high efficacy in Japanese patients with HCV genotype-1 infection. Moreover, in seven patients with depression who received the 24-week DCV/ASV treatment regimen, the BDI-II scores significantly increased at week 4 as compared with pretreatment values; furthermore, they decreased below baseline at week 12 despite the rapid decline of serum HCV levels after the initiation of DCV/ASV therapy. The BDI-II scores gradually decreased during therapy in the remaining 77 DCV/ASV-treated patients without depression. The BDI-II scores showed a significant decrease from baseline to the end of treatment with 12-week regimens, including SOF/LDV and EBR/GZR. The 12-week DAA regimen of SOF/LDV and EBR/GZR can be safely used with high efficacy in patients with genotype-1 HCV infection, including those with depression.Entities:
Keywords: BDI-II; HCV genotype 1; depression; direct-acting antiviral agents; sustained virological response
Year: 2018 PMID: 30210615 PMCID: PMC6122593 DOI: 10.3892/etm.2018.6481
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447