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Clin Mol Hepatol. 2024;30(3):487-499.

Evolutionary changes in metabolic dysfunction-associated steatotic liver disease and risk of hepatocellular carcinoma: A nationwide cohort study.

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제1저자 정석송 · 교신저자 김원, 박상민

소속 (12)
  1. Department of Biomedical Informatics, Korea University College of Medicine, Seoul, Korea.
  2. Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
  3. Department of Family Medicine, College of Medicine, Chung-Ang University Gwangmyeong Hospital, Chung-Ang University College of Medicine, Gwangmyeong, Korea.
  4. Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
  5. Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
  6. Department of Family Medicine, Life Clinic, Seoul, Korea.
  7. Department of Internal Medicine, Hanyang University Hospital, Seoul, Korea.
  8. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul, Korea.
  9. Department of Liver Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  10. The International Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
  11. National Center for Liver Cancer, Shanghai, China.
  12. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

Abstract

BACKGROUND/AIMS To determine the association between evolutionary changes in metabolic dysfunction-associated steatotic liver disease (MASLD) status and the risk of hepatocellular carcinoma (HCC) in a nationwide population-based cohort.

METHODS Information on study participants was derived from the Korea National Health Insurance Service database. The study population consisted of 5,080,410 participants who underwent two consecutive biennial health screenings between 2009 and 2012. All participants were followed up until HCC, death, or 31 December 2020. The association of evolutionary changes in MASLD status, as assessed by the fatty liver index and cardiometabolic risk factors, including persistent non-MASLD, resolved MASLD, incident MASLD, and persistent MASLD, with HCC risk was evaluated using multivariable-adjusted Cox proportional hazards regression.

RESULTS Among the 5,080,410 participants with 39,910,331 person-years of follow-up, 4,801 participants developed HCC. The incidence of HCC in participants with resolved, incident, and persistent MASLD was approximately 2.2-, 2.3-, and 4.7-fold higher, respectively, than that in those with persistent non-MASLD among the Korean adult population. When stratifying the participants according to the evolutionary change in MASLD status, persistent (adjusted hazard ratio [aHR], 2.94; 95% confidence interval [CI], 2.68-3.21; P<0.001), incident (aHR, 1.85; 95% CI, 1.63-2.10; P<0.001), and resolved MASLD (aHR, 1.33; 95% CI, 1.18-1.50; P<0.001) had an increased risk of HCC compared to persistent non-MASLD.

CONCLUSION The evolutionary changes in MASLD were associated with the differential risk of HCC independent of metabolic risk factors and concomitant medications, providing additional information on the risk of HCC stratification in patients with MASLD.

Keywords

Cohort studiesEpidemiologyFatty liverLiver neoplasms

Figures

Figure 1.
Figure 1. Flow diagram of study participants selected from the Korea National Health Insurance Service database.
Figure 2.
Figure 2. Cumulative incidence function according to the evolutionary changes in MASLD status. MASLD, metabolic dysfunctionassociated steatotic liver disease.
Figure 3.
Figure 3. A forest plot on the impact of evolutionary changes in MASLD status on the risk of HCC stratified by risk factors for HCC. Data are adjusted hazard ratio (95% confidence interval) calculated using the Cox proportional hazards model after adjustments for baseline fatty liver index, age, sex, household income, body mass index, systolic blood pressure, fasting serum glucose, cigarette smoking, exercise frequency, CCI, antihypertensive medication, antidiabetic medication, antidyslipidemic medication, aspirin, acetaminophen, NSAIDs, and advanced fibrosis. MASLD, metabolic dysfunction-associated steatotic liver disease; CCI, Charlson comorbidity index; NSAIDs, non-steroidal anti-inflammatory drugs.

그림 출처: PubMed Central 공개 논문 (PMC11261234)

Comment · 정정

Conflict of interest statement

Conflicts of Interest . The authors have no conflicts to disclose.

그 밖의 정보
출판 형태
Journal Article
저널
Clinical and molecular hepatology · eISSN 2287-285X
전자 출판
2024-05-07
MeSH
Humans · Carcinoma, Hepatocellular* / pathology / diagnosis / complications · Liver Neoplasms* / diagnosis / pathology / complications · Male · Female · Middle Aged · Risk Factors · Republic of Korea / epidemiology · Adult · Incidence · Proportional Hazards Models · Fatty Liver / complications / diagnosis · Aged · Cohort Studies
연구비
Ministry of Science and ICT · Institute for Information & Communications Technology Planning & Evaluation · National Research Foundation of Korea 2021R1F1A1063346 · National Research Foundation of Korea 2021R1A2C2005820 · National Research Foundation of Korea 2021M3A9E4021818 · National Research Foundation of Korea RS-2023-00237783 · Korea Health Industry Development Institute · Ministry of Health and Welfare HI21C0538 · Korea National Institute of Health 2022ER090202 · Seoul National University Hospital 04-2021-0370
참고문헌
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