Your browser doesn't support javascript.
loading
Metabolic management after sustained virologic response in elderly patients with hepatitis C virus: A multicenter study.
Sano, Tomoya; Amano, Keisuke; Ide, Tatsuya; Isoda, Hiroshi; Honma, Yuichi; Morita, Yasuyo; Yano, Yoichi; Nakamura, Hiroki; Itano, Satoshi; Miyajima, Ichiro; Shirachi, Miki; Kuwahara, Reiichiro; Ohno, Miki; Kawaguchi, Toshihiro; Tsutsumi, Tsubasa; Nakano, Dan; Arinaga-Hino, Teruko; Kawaguchi, Machiko; Eguchi, Yuichiro; Torimura, Takuji; Takahashi, Hirokazu; Harada, Masaru; Kawaguchi, Takumi.
Afiliación
  • Sano T; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
  • Amano K; Fukuoka Consulting and Support Center for Liver Diseases, Kurume, Japan.
  • Ide T; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
  • Isoda H; Fukuoka Consulting and Support Center for Liver Diseases, Kurume, Japan.
  • Honma Y; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
  • Morita Y; Fukuoka Consulting and Support Center for Liver Diseases, Kurume, Japan.
  • Yano Y; Department of Gastroenterology, Kurume University Medical Center, Kurume, Japan.
  • Nakamura H; Liver Center, Saga University Hospital, Faculty of Medicine, Saga University, Saga, Japan.
  • Itano S; Third Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
  • Miyajima I; Department of Gastroenterology, Nagata Hospital, Yanagawa, Japan.
  • Shirachi M; Division of Gastroenterology, Department of Medicine, Saga Central Hospital, Saga, Japan.
  • Kuwahara R; Department of Gastroenterology, Shin Koga Hospital, Kurume, Japan.
  • Ohno M; Department of Gastroenterology, Kurume Chuo Hospital, Kurume, Japan.
  • Kawaguchi T; Department of Gastroenterology, Kumamoto Central Hospital, Kikuchi, Japan.
  • Tsutsumi T; Department of Gastroenterology, Chikugo City Hospital, Chikugo, Japan.
  • Nakano D; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
  • Arinaga-Hino T; Department of Gastroenterology, Oita Saiseikai Hita Hospital, Hita, Japan.
  • Kawaguchi M; Department of Gastroenterology and Hepatology, Yanagawa Hospital, Yanagawa, Japan.
  • Eguchi Y; Division of Gastroenterology, Department of Medicine, Social Insurance Tagawa Hospital, Tagawa, Japan.
  • Torimura T; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
  • Takahashi H; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
  • Harada M; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
  • Kawaguchi T; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
Hepatol Res ; 54(4): 326-335, 2024 Apr.
Article en En | MEDLINE | ID: mdl-37975277
AIMS: Hepatocellular carcinoma (HCC) develops even in patients with hepatitis C virus (HCV) eradication by direct-acting antiviral agents. Fatty liver and metabolic dysfunction are becoming major etiologies of HCC. We aimed to evaluate the impact of metabolic dysfunction-associated steatotic liver disease (MASLD), a new definition of steatotic liver disease, on the development of HCC after HCV eradication. METHODS: We enrolled 1280 elderly patients with HCV eradication and no history of HCC. We evaluated α-fetoprotein (AFP), Fibrosis-4 index and MASLD after 24 weeks of sustained virological response. Decision tree analysis was used to investigate factors associated with HCC development after HCV eradication. RESULTS: A total of 86 patients (6.7%) developed HCC during the follow-up period (35.8 ± 23.7 months). On multivariate analysis, serum AFP level (HR 1.08, CI 1.04-1.11, P = 0.0008), Fibrosis-4 index (HR 1.17, CI 1.08-1.26, P = 0.0007), and MASLD (HR 3.04, CI 1.40-6.58, P = 0.0125) at 24 weeks of sustained virological response were independent factors associated with HCC development. In decision tree analysis, the initial classifier for HCC development was AFP ≥7 ng/mL. However, in patients with AFP <7 ng/mL, MASLD, rather than Fibrosis-4 index, was the classifier for HCC development. No significant difference was observed in the cumulative incidence of HCC between patients with AFP ≥7 ng/mL and patients with AFP <7 ng/mL and MASLD. CONCLUSION: MASLD at 24 weeks of sustained virological response is a risk factor for HCC development in elderly patients with HCV eradication. Additionally, decision tree analysis revealed that MASLD was associated with HCC development, even in patients with serum AFP levels <7 ng/mL.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Hepatol Res Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Hepatol Res Año: 2024 Tipo del documento: Article País de afiliación: Japón