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Hepatic inflammation and fibrosis are profiles related to mid-term mortality in biopsy-proven MASLD: A multicenter study in Japan.
Tsutsumi, Tsubasa; Kawaguchi, Takumi; Fujii, Hideki; Kamada, Yoshihiro; Takahashi, Hirokazu; Kawanaka, Miwa; Sumida, Yoshio; Iwaki, Michihiro; Hayashi, Hideki; Toyoda, Hidenori; Oeda, Satoshi; Hyogo, Hideyuki; Morishita, Asahiro; Munekage, Kensuke; Kawata, Kazuhito; Sawada, Koji; Maeshiro, Tatsuji; Tobita, Hiroshi; Yoshida, Yuichi; Naito, Masafumi; Araki, Asuka; Arakaki, Shingo; Noritake, Hidenao; Ono, Masafumi; Masaki, Tsutomu; Yasuda, Satoshi; Tomita, Eiichi; Yoneda, Masato; Tokushige, Akihiro; Ueda, Shinichiro; Aishima, Shinichi; Nakajima, Atsushi; Okanoue, Takeshi.
Afiliación
  • Tsutsumi T; 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.
  • Fujii H; Department of Hepatology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
  • Kamada Y; Department of Advanced Metabolic Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Takahashi H; Liver Center, Saga Medical School, Saga University, Saga, Japan.
  • Kawanaka M; Department of General Internal Medicine2, Kawasaki Medical Center, Okayama, Japan.
  • Sumida Y; Graduate School of Healthcare Management, International University of Healthcare and Welfare, Minato-ku, Japan.
  • Iwaki M; Department of Gastroenterology and Hepatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Hayashi H; Department of Gastroenterology and Hepatology, Gifu Municipal Hospital, Gifu, Japan.
  • Toyoda H; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Oeda S; Liver Center, Saga Medical School, Saga University, Saga, Japan.
  • Hyogo H; Department of Laboratory Medicine, Saga University Hospital, Saga, Japan.
  • Morishita A; Hyogo Life Care Clinic, Hiroshima, Japan.
  • Munekage K; Department of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
  • Kawata K; Department of Gastroenterology, Hata Kenmin Hospital, Sukumo, Japan.
  • Sawada K; Hepatology Division, Department of Internal Medicine II, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Maeshiro T; Division of Metabolism and Biosystemic Science, Gastroenterology, and Hematology/Oncology, Department of Medicine, Asahikawa Medical University, Asahikawa, Japan.
  • Tobita H; First Department of Internal Medicine, Division of Infectious, Respiratory, and Digestive Medicine, University of the Ryukyus Graduate School of Medicine, Nishihara, Japan.
  • Yoshida Y; Department of Pathology, Shimane University Hospital, Izumo, Japan.
  • Naito M; Department of Gastroenterology and Hepatology, Suita Municipal Hospital, Osaka, Japan.
  • Araki A; Department of Gastroenterology and Hepatology, Suita Municipal Hospital, Osaka, Japan.
  • Arakaki S; Department of Pathology, Shimane University Hospital, Izumo, Japan.
  • Noritake H; First Department of Internal Medicine, Division of Infectious, Respiratory, and Digestive Medicine, University of the Ryukyus Graduate School of Medicine, Nishihara, Japan.
  • Ono M; Hepatology Division, Department of Internal Medicine II, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Masaki T; Division of Innovative Medicine for Hepatobiliary & Pancreatology, Faculty of Medicine, Kagawa University, Kita, Japan.
  • Yasuda S; Department of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
  • Tomita E; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Yoneda M; Department of Gastroenterology and Hepatology, Gifu Municipal Hospital, Gifu, Japan.
  • Tokushige A; Department of Gastroenterology and Hepatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Ueda S; Department of Clinical Pharmacology and Therapeutics, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
  • Aishima S; Department of Clinical Pharmacology and Therapeutics, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
  • Nakajima A; Department of Scientific Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Okanoue T; Department of Gastroenterology and Hepatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Aliment Pharmacol Ther ; 59(12): 1559-1570, 2024 06.
Article en En | MEDLINE | ID: mdl-38651312
ABSTRACT

AIMS:

A multi-stakeholder consensus has proposed MASLD (metabolic dysfunction-associated steatotic liver disease). We aimed to investigate the pathological findings related to the mid-term mortality of patients with biopsy-proven MASLD in Japan.

METHODS:

We enrolled 1349 patients with biopsy-proven MASLD. The observational period was 8010 person years. We evaluated independent factors associated with mortality in patients with MASLD by Cox regression analysis. We also investigated pathological profiles related to mortality in patients with MASLD using data-mining analysis.

RESULTS:

The prevalence of MASH and stage 3/4 fibrosis was observed in 65.6% and 17.4%, respectively. Forty-five patients with MASLD died. Of these, liver-related events were the most common cause at 40% (n = 18), followed by extrahepatic malignancies at 26.7% (n = 12). Grade 2/3 lobular inflammation and stage 3/4 fibrosis had a 1.9-fold and 1.8-fold risk of mortality, respectively. In the decision-tree analysis, the profiles with the worst prognosis were characterised by Grade 2/3 hepatic inflammation, along with advanced ballooning (grade 1/2) and fibrosis (stage 3/4). This profile showed a mortality at 8.3%. Furthermore, the random forest analysis identified that hepatic fibrosis and inflammation were the first and second responsible factors for the mid-term prognosis of patients with MASLD.

CONCLUSIONS:

In patients with biopsy-proven MASLD, the prevalence of MASH and advanced fibrosis was approximately 65% and 20%, respectively. The leading cause of mortality was liver-related events. Hepatic inflammation and fibrosis were significant factors influencing mid-term mortality. These findings highlight the importance of targeting inflammation and fibrosis in the management of patients with MASLD.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cirrosis Hepática Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Aliment Pharmacol Ther Asunto de la revista: FARMACOLOGIA / GASTROENTEROLOGIA / TERAPIA POR MEDICAMENTOS Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cirrosis Hepática Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Aliment Pharmacol Ther Asunto de la revista: FARMACOLOGIA / GASTROENTEROLOGIA / TERAPIA POR MEDICAMENTOS Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido