Hepatology. 2025;81(1):228-237.
MASLD/MetALD and mortality in individuals with any cardio-metabolic risk factor: A population-based study with 26.7 years of follow-up.
제1저자 곽민선 · 교신저자 양주동
소속 (5)
- Department of Internal Medicine, Healthcare Research Institute, Healthcare System Gangnam Center, Seoul National University Hospital, Seoul, Republic of Korea.
- Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California, USA.
- Division of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
- Houston Methodist Hospital, Houston, Texas, USA.
- Department of Houston Research Institute, Houston, Texas, USA.
Abstract
BACKGROUND AND AIMS A new term, metabolic dysfunction-associated steatotic liver disease (MASLD), has been proposed by a multi-society expert panel. However, it remains unclear whether hepatic steatosis per se in MASLD contributes to an increased risk of mortality in individuals with any cardio-metabolic risk factor (CMRF), which is also a significant risk factor for increased mortality. This study aimed to compare all-cause and cause-specific mortality between the "MASLD/MetALD" and "no steatotic liver disease (SLD)" groups in individuals with any CMRF.
APPROACH AND RESULTS A population-based cohort study was conducted using 10,750 participants of the Third National Health and Nutrition Examination Survey. All-cause and cause-specific (cardiovascular, cancer, diabetes, and liver) mortality risks were compared between the "MASLD," "MetALD," and "no SLD" groups using the Cox proportional hazards model with complex survey design weights, adjusted for confounders. Over 26 years, the "MASLD" group did not show significantly increased all-cause (adjusted HR 1.04[95% CI: 0.95-1.14], p = 0.413), cardiovascular (0.88 [0.75-1.04], p = 0.139), or cancer (1.06[0.84-1.33], p = 0.635) mortality risk compared to the "no SLD" group in individuals with any CMRF. The MetALD group was associated with increased all-cause (1.41 [1.05-1.89], p = 0.022), cancer (2.35 [1.33-4.16], p = 0.004), and liver (15.04 [2.96-76.35], p = 0.002) mortality risk compared with the no SLD group. This trend was more pronounced in the MetALD group with advanced fibrosis assessed by Fibrosis-4 (FIB-4).
CONCLUSIONS In individuals with CMRF, the presence of steatotic liver disease (MASLD) alone did not increase the risk of mortality, except in cases with more alcohol consumption (MetALD). Therefore controlling metabolic risk factors and reducing alcohol consumption in people with MASLD or MetALD will be crucial steps to improve long-term health outcomes.
Copyright © 2024 American Association for the Study of Liver Diseases.
Conflict of interest statement
Conflict of interest statements: Zhenghui Gordon Jiang consults for Olix. He received grants from Pfizer and Gilead. He owns intellectual property rights in Labcorp. Hirsh D. Trivedi consults for Novo Nordisk. Mazen Noureddin consults, advises, and received grants from Altimmune, Boehringer Ingelheim, Cytodyn, 89Bio, GlaxoSmithKline, Medigal, Merck, Novo Nordisk, Terns, and Takeda. He owns stock in Rivus Pharma, Cytodyn, and ChronWell. Ju Dong Yang consults for AstraZeneca, Eisai, Exact and FujiFilm Medical Sciences. The remaining authors have nothing to report.
그 밖의 정보
- 출판 형태
- Journal Article
- 저널
- Hepatology (Baltimore, Md.) · eISSN 1527-3350
- 전자 출판
- 2024-05-13
- MeSH
- Humans · Male · Female · Middle Aged · Follow-Up Studies · Adult · Nutrition Surveys* · Fatty Liver / mortality / complications · Cardiovascular Diseases / mortality · Cardiometabolic Risk Factors · Risk Factors · Cause of Death · Cohort Studies · United States / epidemiology · Aged · Proportional Hazards Models
- 연구비
- NIDDK NIH HHS K08 DK115883 · NIDDK NIH HHS L30 DK118655 · NIAAA NIH HHS R01 AA030770
- 참고문헌
- 24편