Baseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis C
Abstract We previously revealed that Angiopoietin-2 (Ang2) predicts non-regression of liver fibrosis based on liver stiffness measurement (LSM) at 24 weeks after anti-hepatitis C virus (HCV) treatment. In this study, we extended the observational period to 96 weeks to investigate the factors associa...
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2021
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oai:doaj.org-article:9f05ad0e9c3c4bdcaf4b034a07202f1e2021-12-02T17:39:31ZBaseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis C10.1038/s41598-021-88632-72045-2322https://doaj.org/article/9f05ad0e9c3c4bdcaf4b034a07202f1e2021-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-88632-7https://doaj.org/toc/2045-2322Abstract We previously revealed that Angiopoietin-2 (Ang2) predicts non-regression of liver fibrosis based on liver stiffness measurement (LSM) at 24 weeks after anti-hepatitis C virus (HCV) treatment. In this study, we extended the observational period to 96 weeks to investigate the factors associated with non-regression after treatment with direct-acting-antivirals (DAAs). Patients treated with DAAs who underwent transient elastography at baseline and 24 and 96 weeks after DAA therapy were included. Baseline and post-treatment serum Ang2 levels were measured. Liver fibrosis stages were defined based on LSM. Multivariate regression was used to evaluate factors associated with non-regression of liver fibrosis between various time points. In total, 110 patients were included. Of these, 11% showed non-regression of LSM-based fibrosis stage at 96 weeks after DAA therapy. In multivariate analysis, advanced liver fibrosis stage and high baseline Ang2 levels were significantly associated with non-regression at 96 weeks. In patients with advanced liver fibrosis (F3/4), baseline Ang2 levels were associated with non-regression of liver fibrosis stage. Between SVR24 and SVR96, post-treatment Ang2 levels and controlled attenuation parameter values at SVR24 were significantly associated with non-regression of liver fibrosis stage in patients with F3/4. Thus, serum Ang2 levels are an important target for monitoring and therapy.Naoki KawagishiGoki SudaMegumi KimuraOsamu MaeharaRen YamadaYoshimasa TokuchiAkinori KuboTakashi KitagatayaTaku ShigesawaKazuharu SuzukiMasatsugu OharaMasato NakaiTakuya ShoMitsuteru NatsuizakaKenichi MorikawaKoji OgawaYusuke KudoMutsumi NishidaNaoya SakamotoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021) |
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Medicine R Science Q Naoki Kawagishi Goki Suda Megumi Kimura Osamu Maehara Ren Yamada Yoshimasa Tokuchi Akinori Kubo Takashi Kitagataya Taku Shigesawa Kazuharu Suzuki Masatsugu Ohara Masato Nakai Takuya Sho Mitsuteru Natsuizaka Kenichi Morikawa Koji Ogawa Yusuke Kudo Mutsumi Nishida Naoya Sakamoto Baseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis C |
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Abstract We previously revealed that Angiopoietin-2 (Ang2) predicts non-regression of liver fibrosis based on liver stiffness measurement (LSM) at 24 weeks after anti-hepatitis C virus (HCV) treatment. In this study, we extended the observational period to 96 weeks to investigate the factors associated with non-regression after treatment with direct-acting-antivirals (DAAs). Patients treated with DAAs who underwent transient elastography at baseline and 24 and 96 weeks after DAA therapy were included. Baseline and post-treatment serum Ang2 levels were measured. Liver fibrosis stages were defined based on LSM. Multivariate regression was used to evaluate factors associated with non-regression of liver fibrosis between various time points. In total, 110 patients were included. Of these, 11% showed non-regression of LSM-based fibrosis stage at 96 weeks after DAA therapy. In multivariate analysis, advanced liver fibrosis stage and high baseline Ang2 levels were significantly associated with non-regression at 96 weeks. In patients with advanced liver fibrosis (F3/4), baseline Ang2 levels were associated with non-regression of liver fibrosis stage. Between SVR24 and SVR96, post-treatment Ang2 levels and controlled attenuation parameter values at SVR24 were significantly associated with non-regression of liver fibrosis stage in patients with F3/4. Thus, serum Ang2 levels are an important target for monitoring and therapy. |
format |
article |
author |
Naoki Kawagishi Goki Suda Megumi Kimura Osamu Maehara Ren Yamada Yoshimasa Tokuchi Akinori Kubo Takashi Kitagataya Taku Shigesawa Kazuharu Suzuki Masatsugu Ohara Masato Nakai Takuya Sho Mitsuteru Natsuizaka Kenichi Morikawa Koji Ogawa Yusuke Kudo Mutsumi Nishida Naoya Sakamoto |
author_facet |
Naoki Kawagishi Goki Suda Megumi Kimura Osamu Maehara Ren Yamada Yoshimasa Tokuchi Akinori Kubo Takashi Kitagataya Taku Shigesawa Kazuharu Suzuki Masatsugu Ohara Masato Nakai Takuya Sho Mitsuteru Natsuizaka Kenichi Morikawa Koji Ogawa Yusuke Kudo Mutsumi Nishida Naoya Sakamoto |
author_sort |
Naoki Kawagishi |
title |
Baseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis C |
title_short |
Baseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis C |
title_full |
Baseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis C |
title_fullStr |
Baseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis C |
title_full_unstemmed |
Baseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis C |
title_sort |
baseline elevated serum angiopoietin-2 predicts long-term non-regression of liver fibrosis after direct-acting antiviral therapy for hepatitis c |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/9f05ad0e9c3c4bdcaf4b034a07202f1e |
work_keys_str_mv |
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