Influence of alcohol on newly developed metabolic dysfunction-associated fatty liver disease in both sexes: A longitudinal study

• Published in: Clinical nutrition (Edinburgh, Scotland) Vol. 42; no. 5; pp. 810 - 816
• Main Authors: Sogabe, Masahiro, Okahisa, Toshiya, Kagawa, Miwako, Ueda, Hiroyuki, Kagemoto, Kaizo, Tanaka, Hironori, Kida, Yoshifumi, Tomonari, Tetsu, Taniguchi, Tatsuya, Okamoto, Koichi, Miyamoto, Hiroshi, Sato, Yasushi, Nakasono, Masahiko, Takayama, Tetsuji
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.05.2023
• Subjects: Ages; Alcohol drinking; alcohols; clinical nutrition; cohort studies; confidence interval; Ethanol; fatty liver; Female; fibrosis; Food; Humans; liver cirrhosis; Liver diseases; Longitudinal Studies; Male; Non-alcoholic Fatty Liver Disease - epidemiology; odds ratio; Onset; protective effect; Risk Factors; Sex; Alcohol drinking; Liver diseases; Ages; Sex; Onset
• ISSN: 0261-5614; 1532-1983; 1532-1983
• DOI: 10.1016/j.clnu.2023.03.020

The influence of changes in alcohol consumption on newly developed metabolic dysfunction-associated fatty liver disease (MAFLD) is unclear. We investigated the influence of alcohol consumption on newly developed MAFLD in both sexes. This observational cohort study included 4071 patients who underwent more than two health check-ups between 2015 and 2020 over an interval of more than a year. Generalised estimating equations were used for analyses. At baseline, the rates of drinking and MAFLD between men and women were 72.5% versus 41.7% and 42.2% versus 22.1%, respectively. At the most recent stage, the rates of an increase in alcohol consumption for men and women were 13.3% and 8.7%, respectively, and 311/1192 (26.1%) men and 155/1566 (9.9%) women had newly developed MAFLD. The odds ratio (OR) for drinking in patients with newly developed MAFLD was 0.863 (men) (95% confidence interval [CI], 0.676–1.102, p = 0.237) and 1.041 (women) (95% CI, 0.753–1.439, p = 0.808); the OR for women who drank 140–279.9 g/week was 2.135 (95% CI, 1.158–3.939, p < 0.05) and that for all drinking categories among women was >1. Several non-invasive fibrosis scores were significantly associated with the quantity of alcohol consumption in patients with newly developed MAFLD (p < 0.005). Alcohol consumption had no significant protective effect against newly developed MAFLD in both sexes, regardless of quantity. Conversely, alcohol consumption ≥140 g/week was a risk factor for newly developed MAFLD in women. The development of liver fibrosis with increased alcohol intake should be considered in patients with MAFLD.