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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

Interpretation of metabolic dysfunction and alcohol-related liver disease: Position statement by an expert panel on alcohol-related liver disease (2024 edition)

DOI: 10.12449/JCH250308
Research funding:

Noncommunicable Chronic Diseases-National Science and Technology Major Project (2023ZD0508704)

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  • Corresponding author: LI Jie, lijier@nju.edu.cn (ORCID: 0000-0003-0973-8645); SHI Junping, 20131004@hznu.edu.cn (ORCID: 0000-0001-9434-897X)
  • Received Date: 2025-02-20
  • Accepted Date: 2025-03-18
  • Published Date: 2025-03-25
  • In November 2024, the Expert Group on Alcohol-related Liver Disease released a position statement on metabolic dysfunction and alcohol-related liver disease (MetALD). MetALD is a new subtype of steatotic liver disease and refers to MASLD patients with a relatively large amount of alcohol consumption. The position statement points out the importance of accurate evaluation of alcohol consumption and recommends to quantify alcohol consumption using standard methods and alcohol biomarkers, and a comprehensive diagnosis should be made based on metabolic risk factors. In addition, the position statement analyzes the influence of drinking pattern on the diagnosis of MetALD and recommends to consider long-term drinking history during typing. The position statement also discusses the complex association between drinking and the diseases including metabolic syndrome, hepatic steatosis, fibrosis, and type 2 diabetes mellitus, and it is pointed out that the hierarchical management of patients should be optimized based on liver histological models and noninvasive models. The position statement elaborates on the definition of MetALD, drinking assessment, the interaction between alcohol use and metabolic dysfunction, and the methods for comprehensive management of MetALD, in order to facilitate learning and provide guidance for clinicians and researchers in clinical practice.

     

  • [1]
    RINELLA ME, LAZARUS JV, RATZIU V, et al. A multisociety Delphi consensus statement on new fatty liver disease nomenclature[J]. Ann Hepatol, 2024, 29( 1): 101133. DOI: 10.1016/j.aohep.2023.101133.
    [2]
    ARAB JP, LA DÍAZ, REHM J, et al. Metabolic dysfunction and alcohol-related liver disease(MetALD): Position statement by an expert panel on alcohol-related liver disease[J]. J Hepatol, 2024. DOI: 10.1016/j.jhep.2024.11.028.[ Online ahead of print]
    [3]
    What’s a standard drink measurment?[EB/OL].[ 2025-02-19]. https://rethinkingdrinking.‍niaaa.‍nih.‍gov/how-much-too-much/whats-standard-drink. https://rethinkingdrinking.‍niaaa.‍nih.‍gov/how-much-too-much/whats-standard-drink
    [4]
    PARADIS C, BUTT P, SHIELD K, et al. Canada’s guidance on alcohol and health[EB/OL].[ 2025-02-19]. https://www.ccsa.ca/canadas-guidance-alcohol-and-health. https://www.ccsa.ca/canadas-guidance-alcohol-and-health
    [5]
    SKINNER HA, SHEU WJ. Reliability of alcohol use indices. The lifetime drinking history and the MAST[J]. J Stud Alcohol, 1982, 43( 11): 1157- 1170. DOI: 10.15288/jsa.1982.43.1157.
    [6]
    BUSH K, KIVLAHAN DR, MCDONELL MB, et al. The AUDIT alcohol consumption questions(AUDIT-C): An effective brief screening test for problem drinking. Ambulatory Care Quality Improvement Project(ACQUIP). Alcohol Use Disorders Identification Test[J]. Arch Intern Med, 1998, 158( 16): 1789- 1795. DOI: 10.1001/archinte.158.16.1789.
    [7]
    LOUVET A, BOURCIER V, ARCHAMBEAUD I, et al. Low alcohol consumption influences outcomes in individuals with alcohol-related compensated cirrhosis in a French multicenter cohort[J]. J Hepatol, 2023, 78( 3): 501- 512. DOI: 10.1016/j.jhep.2022.11.013.
    [8]
    JONES AW. Brief history of the alcohol biomarkers CDT, EtG, EtS, 5-HTOL, and PEth[J]. Drug Test Anal, 2024, 16( 6): 570- 587. DOI: 10.1002/dta.3584.
    [9]
    HARRIS JC, LEGGIO L, FAROKHNIA M. Blood biomarkers of alcohol use: A scoping review[J]. Curr Addict Rep, 2021, 8( 4): 500- 508. DOI: 10.1007/s40429-021-00402-7.
    [10]
    FAKHARI S, WASZKIEWICZ N. Old and new biomarkers of alcohol abuse: Narrative review[J]. J Clin Med, 2023, 12( 6): 2124. DOI: 10.3390/jcm12062124.
    [11]
    GREEN EW, BYERS IS, DEUTSCH-LINK S. Closing the care gap: Management of alcohol use disorder in patients with alcohol-associated liver disease[J]. Clin Ther, 2023, 45( 12): 1189- 1200. DOI: 10.1016/j.clinthera.2023.09.017.
    [12]
    World Health Organization. Global Status Report on Alcohol and Health 2018[R]. Geneva: World Health Organization, 2019.
    [13]
    KIM HS, XIAO XJ, BYUN J, et al. Synergistic associations of PNPLA3 I148M variant, alcohol intake, and obesity with risk of cirrhosis, hepatocellular carcinoma, and mortality[J]. JAMA Netw Open, 2022, 5( 10): e2234221. DOI: 10.1001/jamanetworkopen.2022.34221.
    [14]
    DING CY, NG FAT L, BRITTON A, et al. Binge-pattern alcohol consumption and genetic risk as determinants of alcohol-related liver disease[J]. Nat Commun, 2023, 14: 8041. DOI: 10.1038/s41467-023-43064-x.
    [15]
    LLAMOSAS-FALCÓN L, REHM J, BRIGHT S, et al. The relationship between alcohol consumption, BMI, and type 2 diabetes: A systematic review and dose-response meta-analysis[J]. Diabetes Care, 2023, 46( 11): 2076- 2083. DOI: 10.2337/dc23-1015.
    [16]
    PARKER R, AITHAL GP, BECKER U, et al. Natural history of histologically proven alcohol-related liver disease: A systematic review[J]. J Hepatol, 2019, 71( 3): 586- 593. DOI: 10.1016/j.jhep.2019.05.020.
    [17]
    HAGSTRÖM H, THIELE M, ROELSTRAETE B, et al. Mortality in biopsy-proven alcohol-related liver disease: A population-based nationwide cohort study of 3 453 patients[J]. Gut, 2021, 70( 1): 170- 179. DOI: 10.1136/gutjnl-2019-320446.
    [18]
    SIMON TG, ROELSTRAETE B, KHALILI H, et al. Mortality in biopsy-confirmed nonalcoholic fatty liver disease: Results from a nationwide cohort[J]. Gut, 2021, 70( 7): 1375- 1382. DOI: 10.1136/gutjnl-2020-322786.
    [19]
    TAYLOR RS, TAYLOR RJ, BAYLISS S, et al. Association between fibrosis stage and outcomes of patients with nonalcoholic fatty liver disease: A systematic review and meta-analysis[J]. Gastroenterology, 2020, 158( 6): 1611- 1625. e 12. DOI: 10.1053/j.gastro.2020.01.043.
    [20]
    European Association for the Study of the Liver. Reply to: Correspondence on“EASL Clinical Practice Guidelines on non-invasive tests for evaluation of liver disease severity and prognosis-2021 update”[J]. J Hepatol, 2022, 76( 1): 251- 252. DOI: 10.1016/j.jhep.2021.10.008.
    [21]
    STERLING RK, DUARTE-ROJO A, PATEL K, et al. AASLD Practice Guideline on imaging-based noninvasive liver disease assessment of hepatic fibrosis and steatosis[J]. Hepatology, 2025, 81( 2): 672- 724. DOI: 10.1097/HEP.0000000000000843.
    [22]
    LEE AK, BOBB JF, RICHARDS JE, et al. Integrating alcohol-related prevention and treatment into primary care: A cluster randomized implementation trial[J]. JAMA Intern Med, 2023, 183( 4): 319- 328. DOI: 10.1001/jamainternmed.2022.7083.
    [23]
    SIMPSON RF, HERMON C, LIU B, et al. Alcohol drinking patterns and liver cirrhosis risk: Analysis of the prospective UK Million Women Study[J]. Lancet Public Health, 2019, 4( 1): e41- e48. DOI: 10.1016/S2468-2667(18)30230-5.
    [24]
    BECKER U, DEIS A, SØRENSEN TI, et al. Prediction of risk of liver disease by alcohol intake, sex, and age: A prospective population study[J]. Hepatology, 1996, 23( 5): 1025- 1029. DOI: 10.1002/hep.510230513.
    [25]
    DESALEGN H, DIAZ LA, REHM J, et al. Impact of alcohol use on liver disease outcomes[J]. Clin Liver Dis(Hoboken), 2024, 23( 1): e0192. DOI: 10.1097/CLD.0000000000000192.
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