Hepatic inflammation and fibrosis are profiles related to mid‐term mortality in biopsy‐proven MASLD: A multicenter study in Japan

Author:

Tsutsumi Tsubasa1ORCID,Kawaguchi Takumi1,Fujii Hideki2,Kamada Yoshihiro3,Takahashi Hirokazu4,Kawanaka Miwa5,Sumida Yoshio6,Iwaki Michihiro7ORCID,Hayashi Hideki8,Toyoda Hidenori9ORCID,Oeda Satoshi410,Hyogo Hideyuki11,Morishita Asahiro12,Munekage Kensuke13,Kawata Kazuhito14,Sawada Koji15,Maeshiro Tatsuji16,Tobita Hiroshi17,Yoshida Yuichi18,Naito Masafumi18,Araki Asuka17,Arakaki Shingo16,Noritake Hidenao14,Ono Masafumi19,Masaki Tsutomu12,Yasuda Satoshi9,Tomita Eiichi8,Yoneda Masato7,Tokushige Akihiro20,Ueda Shinichiro20,Aishima Shinichi21,Nakajima Atsushi7ORCID,Okanoue Takeshi22

Affiliation:

1. Division of Gastroenterology, Department of Medicine Kurume University School of Medicine Kurume Japan

2. Department of Hepatology Graduate School of Medicine, Osaka Metropolitan University Osaka Japan

3. Department of Advanced Metabolic Hepatology Osaka University Graduate School of Medicine Suita Japan

4. Liver Center Saga Medical School, Saga University Saga Japan

5. Department of General Internal Medicine2 Kawasaki Medical Center Okayama Japan

6. Graduate School of Healthcare Management, International University of Healthcare and Welfare Minato‐ku Japan

7. Department of Gastroenterology and Hepatology Yokohama City University Graduate School of Medicine Yokohama Japan

8. Department of Gastroenterology and Hepatology Gifu Municipal Hospital Gifu Japan

9. Department of Gastroenterology Ogaki Municipal Hospital Ogaki Japan

10. Department of Laboratory Medicine Saga University Hospital Saga Japan

11. Hyogo Life Care Clinic Hiroshima Japan

12. Department of Gastroenterology and Neurology, Faculty of Medicine Kagawa University Kagawa Japan

13. Department of Gastroenterology Hata Kenmin Hospital Sukumo Japan

14. Hepatology Division, Department of Internal Medicine II Hamamatsu University School of Medicine Shizuoka Japan

15. Division of Metabolism and Biosystemic Science, Gastroenterology, and Hematology/Oncology, Department of Medicine Asahikawa Medical University Asahikawa Japan

16. First Department of Internal Medicine, Division of Infectious, Respiratory, and Digestive Medicine University of the Ryukyus Graduate School of Medicine Nishihara Japan

17. Department of Pathology Shimane University Hospital Izumo Japan

18. Department of Gastroenterology and Hepatology Suita Municipal Hospital Osaka Japan

19. Division of Innovative Medicine for Hepatobiliary & Pancreatology, Faculty of Medicine Kagawa University Kita Japan

20. Department of Clinical Pharmacology and Therapeutics Graduate School of Medicine, University of the Ryukyus Okinawa Japan

21. Department of Scientific Pathology Graduate School of Medical Sciences, Kyushu University Fukuoka Japan

22. Hepatology Center, Saiseikai Suita Hospital Suita Japan

Abstract

SummaryAimsA 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.MethodsWe 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.ResultsThe 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.ConclusionsIn 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.

Funder

Japan Agency for Medical Research and Development

Publisher

Wiley

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