Abstract
Acute alcohol consumption is known to exert widespread physiological effects, yet the immediate impacts on metabolic biomarkers remain incompletely understood. The present randomized controlled trial was conducted to investigate the acute effects of a single episode of alcohol ingestion on various biomarkers in healthy individuals. A total of 45 male participants were recruited and randomized into an alcohol group (n = 40) and a control group (n = 5) at an 8:1 ratio. Volunteers in the alcohol group ingested 40% Absolut vodka within 15 min. Blood pressure, heart rate, and blood oxygen saturation were measured at 0 h, 1 h, 3 h, 5 h, 12 h, and 24 h. Venous blood samples were drawn at 0 h, 1 h, 5 h, 12 h, and 24 h after alcohol intake. Our results showed that levels of liver function markers, including α-fucosidase (AFU), albumin (ALB), and alkaline phosphatase (ALP), were significantly increased in the alcohol group compared to the control group. The 24-h area under curve (AUC) of AFU, ALB, and ALP were significantly higher in the alcohol group. The liver fibrosis maker collagen type Ⅳ (Ⅳ-C) tended to be higher at 1 h and 12 h in the alcohol group compared to the control group. Lipid levels, including triglycerides (TG), apolipoprotein A1 (APOA1), and the APOA1/APOB, were significantly elevated after alcohol ingestion, particularly at 5 h and 12 h. The 24 h-AUC of TG, APOA1, and APOA1/APOB were higher in the alcohol group than in the control group. Additionally, cardiac function indicators, including heart rate, systolic blood pressure (SBP), and diastolic blood pressure (DBP), were significantly elevated in the alcohol group. SBP and DBP remained higher 24 h after alcohol ingestion compared to the control group. This study demonstrated that even a single episode of binge drinking could induce significant alterations of biomarkers related to liver function, cardiac function, and lipid profiles. These findings provided valuable insights into the short-term impact of alcohol on health and highlighted the importance of further research to explore the long-term implications of repeated acute alcohol exposure. Given the very small control group, these results should be interpreted as preliminary and confirmed in larger, more balanced randomized trials.
Data availability
The corresponding author can provide an anonymized, de-identified version of the dataset upon reasonable request.
Abbreviations
- Apo A1:
-
Apolipoprotein A1
- Apo B:
-
Apolipoprotein B
- AUC:
-
Areas under the curve
- ALT:
-
Alanine aminotransferase
- AST:
-
Aspartate aminotransferase
- ALP:
-
Alkaline phosphatase
- ALB:
-
Albumin
- BMI:
-
Body mass index
- CHE:
-
Cholinesterase
- CG:
-
Chologlycine acid
- Ⅳ-C:
-
Collagen type IV
- CK:
-
Creatine kinase
- CK-MB:
-
Creatine kinase-MB
- ECM:
-
Extracellular matrix
- GGT:
-
γ-Glutamyl transferase
- HDL:
-
High-density lipoprotein
- HBDH:
-
Hydroxybutyrate dehydrogenase
- LDH:
-
Lactate dehydrogenase
- LN:
-
Laminin
- PⅢNP:
-
Procollagen type III N-terminal peptide
- PRO-C3:
-
Procollagen type III C-peptide
- TBA:
-
Total bile acids
- TC:
-
Total cholesterol
- TG:
-
Triglycerides
- LDL:
-
Low-density lipoprotein
- Lp (a):
-
Lipoprotein (a)
- SBP:
-
Systolic blood pressure
- DBP:
-
Diastolic blood pressure
- Apo A1:
-
Apolipoprotein A1
- Apo B:
-
Apolipoprotein B
- AUC:
-
Areas under the curve
References
Organization, W. H. Global status report on alcohol and health and treatment of substance use disorders. Geneva: WHO. https://www.who.int/publications/i/item/9789240096745. Accessed 25 June 2024. (2024).
Sohi, I. et al. Alcoholic beverage consumption and female breast cancer risk: A systematic review and meta-analysis of prospective cohort studies. Alcohol, Clin. Exp. Res. 48(12), 2222–2241 (2024).
Chan, K. K., Neighbors, C., Gilson, M., Larimer, M. E. & Alan Marlatt, G. Epidemiological trends in drinking by age and gender: Providing normative feedback to adults. Addict. Behav. 32(5), 967–976 (2007).
Wong, R. J. et al. Impact of longitudinal alcohol use patterns on long-term risk of cirrhosis among US veterans with steatotic liver disease. Gastroenterology 166(6), 1156–65 e4 (2024).
Liangpunsakul, S., Qi, R., Crabb, D. W. & Witzmann, F. Relationship between alcohol drinking and aspartate aminotransferase:alanine aminotransferase (AST:ALT) ratio, mean corpuscular volume (MCV), gamma-glutamyl transpeptidase (GGT), and apolipoprotein A1 and B in the U.S. population. J. Stud. Alcohol Drugs 71(2), 249–252 (2010).
Bhandari, B., Zeng, L., Grafenauer, S., Schutte, A. E. & Xu, X. Long-term consumption of 6 different beverages and cardiovascular disease-related mortality: A systematic review and meta-analysis of prospective cohort studies. Curr. Dev. Nutr. 8(3), 102095 (2024).
Han, L. & Jia, J. Long-term effects of alcohol consumption on cognitive function in seniors: A cohort study in China. BMC Geriatr. 21(1), 699 (2021).
Corbin, W. R. et al. In with the old and out with the new? A comparison of the old and new binge drinking standards. Alcohol. Clin. Exp. Res. 38(10), 2657–2663 (2014).
Das, S. K. & Vasudevan, D. M. Alcohol-induced oxidative stress. Life Sci. 81(3), 177–187 (2007).
Stankevic, E. et al. Binge drinking episode causes acute, specific alterations in systemic and hepatic inflammation-related markers. Liver Int. 43(12), 2680–2691 (2023).
Torp, N. et al. Binge drinking induces an acute burst of markers of hepatic fibrogenesis (PRO-C3). Liver Int. 42(1), 92–101 (2022).
Veenstra, J., Ockhuizen, T., van de Pol, H., Wedel, M. & Schaafsma, G. Effects of a moderate dose of alcohol on blood lipids and lipoproteins postprandially and in the fasting state. Alcohol Alcohol 25(4), 371–377 (1990).
Kirpich, I. et al. Binge alcohol-induced microvesicular liver steatosis and injury are associated with down-regulation of hepatic Hdac 1, 7, 9, 10, 11 and up-regulation of Hdac 3. Alcohol. Clin. Exp. Res. 36(9), 1578–1586 (2012).
Jeon, S. & Carr, R. Alcohol effects on hepatic lipid metabolism. J. Lipid Res. 61(4), 470–479 (2020).
Ai, L. et al. Binge alcohol exposure in adolescence impairs normal heart growth. J. Am. Heart Assoc. 9(9), e015611 (2020).
Zaridze, D. et al. Alcohol and mortality in Russia: Prospective observational study of 151,000 adults. Lancet 383(9927), 1465–1473 (2014).
Maudens, K. E. et al. The influence of the body mass index (BMI) on the volume of distribution of ethanol. Forensic Sci. Int. 243, 74–78 (2014).
Schielzeth, H. et al. Robustness of linear mixed‐effects models to violations of distributional assumptions. Methods Ecol. Evol. 11(9), 1141–1152 (2020).
Shremo Msdi, A., Abdul-Mutakabbir, J. C. & Tan, K. K. Characterizing day 1 area under the curve following Vancomycin loading dose administration in adult hospitalized patients using non-trapezoidal linear pharmacokinetic equations: A retrospective observational study. Infect. Dis. Ther. 13(8), 1807–1819 (2024).
Silsirivanit, A. Glycosylation markers in cancer. Adv. Clin. Chem. 89, 189–213 (2019).
Gerlach, J. Hartwig Kuhlenbeck 1897-1984. Appl. Neurophysiol. 48(1–6), VII–XI (1985).
Zhang, W. et al. The applicability of ADA, AFU, and LAC in the early diagnosis and disease risk assessment of hepatitis B-associated liver cirrhosis and hepatocellular carcinoma. Front. Med. (Lausanne). 8, 740029 (2021).
de Jong, W. J. et al. The effect of acute alcohol intoxication on gut wall integrity in healthy male volunteers; a randomized controlled trial. Alcohol 49(1), 65–70 (2015).
Belinskaia, D. A., Voronina, P. A., Shmurak, V. I., Jenkins, R. O. & Goncharov, N. V. Serum albumin in health and disease: Esterase, antioxidant, transporting and signaling properties. Int. J. Mol. Sci. https://doi.org/10.3390/ijms221910318 (2021).
Taivainen, H., Laitinen, K., Tahtela, R., Kilanmaa, K. & Valimaki, M. J. Role of plasma vasopressin in changes of water balance accompanying acute alcohol intoxication. Alcohol. Clin. Exp. Res. 19(3), 759–762 (1995).
Karinch, A. M., Martin, J. H. & Vary, T. C. Acute and chronic ethanol consumption differentially impact pathways limiting hepatic protein synthesis. Am. J. Physiol. Endocrinol. Metab. 295(1), E3-9 (2008).
Schini, M., Vilaca, T., Gossiel, F., Salam, S. & Eastell, R. Bone turnover markers: Basic biology to clinical applications. Endocr. Rev. 44(3), 417–473 (2023).
Brandl, K. et al. Dysregulation of serum bile acids and FGF19 in alcoholic hepatitis. J. Hepatol. 69(2), 396–405 (2018).
Poschl, E. et al. Collagen IV is essential for basement membrane stability but dispensable for initiation of its assembly during early development. Development 131(7), 1619–1628 (2004).
Zhang, F. et al. Association of non-invasive markers with significant fibrosis in patients with nonalcoholic fatty liver disease: A cross-sectional study. Diabetes Metab. Syndr. Obes. 16, 2255–2268 (2023).
Seth, D. et al. Alcohol, signaling, and ECM turnover. Alcohol Clin. Exp. Res. 34(1), 4–18 (2010).
Zdanowicz, K. et al. Increase in serum MMP-9 and TIMP-1 concentrations during alcohol intoxication in adolescents-a preliminary study. Biomolecules 12(5), 710 (2022).
Zhu, C. et al. Correlation of serum liver fibrosis markers with severity of liver dysfunction in liver cirrhosis: a retrospective cross-sectional study. Int. J. Clin. Exp. Med. 8(4), 5989–5998 (2015).
Ma, H. Y., Dong, L., Quan, S. Z., Li, R. Y. & Wang, X. R. Comparison of four markers of hepatic fibrosis and hepatic function indices in patients with liver cirrhosis and hepatoma. Ann. Palliat. Med. 10(4), 4108–4121 (2021).
Fraser, J. R., Laurent, T. C. & Laurent, U. B. Hyaluronan: Its nature, distribution, functions and turnover. J. Intern. Med. 242(1), 27–33 (1997).
Boren, J., Taskinen, M. R., Bjornson, E. & Packard, C. J. Metabolism of triglyceride-rich lipoproteins in health and dyslipidaemia. Nat. Rev. Cardiol. 19(9), 577–592 (2022).
Ontko JA. Effects of ethanol on the metabolism of free fatty acids in isolated liver cells.J Lipid Res.14(1), 78-86 (1973).
Rye, K. A. & Barter, P. J. Regulation of high-density lipoprotein metabolism. Circ. Res. 114(1), 143–156 (2014).
Tall, A. R. & Rader, D. J. Trials and tribulations of CETP inhibitors. Circ. Res. 122(1), 106–112 (2018).
Superko, H. R. Effects of acute and chronic alcohol consumption on postprandial lipemia in healthy normotriglyceridemic men. Am. J. Cardiol. 69(6), 701–704 (1992).
Casillas-Munoz, F. et al. APOA1 and APOB polymorphisms and apolipoprotein concentrations as biomarkers of risk in acute coronary syndrome: Relationship with lipid-lowering therapy effectiveness. Med. Clin. (Barc) 151(1), 1–7 (2018).
Khan, A. A., Lip, G. Y. H. & Shantsila, A. Heart rate variability in atrial fibrillation: The balance between sympathetic and parasympathetic nervous system. Eur. J. Clin. Invest. 49(11), e13174 (2019).
Voskoboinik, A. et al. Acute electrical, autonomic and structural effects of binge drinking: Insights into the “holiday heart syndrome”. Int. J. Cardiol. 331, 100–105 (2021).
Shahoud, J. S., Sanvictores, T., Aeddula, N. R. Physiology, arterial pressure regulation. StatPearls. (2025).
Tasnim, S., Tang, C., Musini, V. M. & Wright, J. M. Effect of alcohol on blood pressure. Cochrane Database Syst. Rev. 7(7), CD012787 (2020).
Ho, M. F. et al. Genome-wide association study for circulating FGF21 in patients with alcohol use disorder: Molecular links between the SNHG16 locus and catecholamine metabolism. Mol. Metab. 63, 101534 (2022).
Acknowledgements
The authors thank all participants in the present study. Furthermore, the authors thank Chenxiang Shi, Yitong Li, Yilin Li, Keyi Wang, Yingchen Wang, Wei Mao, Lili Yuan, Xueyan Cao and Jianing Yan from School of Public Health, and the entire staff from Institute of Nutrition and Health, Zhejiang Chinese Medical University.
Funding
This work was supported by the National Natural Science Foundation of China (NSFC: 82273625), Natural Science Foundation of Zhejiang Province (ZCLY24H2602), Zhejiang Provincial Xinmiao Talents Program (2024R410B061), and National Project for Innovation and Entrepreneurship Training Program for College Students (202410344043; 202410344075X).
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Conceptualization, J.L., S.L. and K.P.; methodology, J.L., K.P.; software, Y.Z., Q.H.; validation K.P., Y.W., and Q.H.; formal analysis, Y.W., Z.L.; investigation, M.Y., Y.Z., D.Z.; data curation, K.P., C.S.; writing-original draft preparation, J.L., K.P., Y.Z.; writing-review and editing, J.L., K.P.; visualization, J.L., S.L.; supervision, K.P., Y.Z.; project administration, J.L., S.L.; All authors have read and agreed to the published version of the manuscript.
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All procedures relative to this study were in accordance with the Helsinki Declaration and approved by the Ethical Committee of Zhejiang Chinese Medical University (20231117–7) and registered at clinicaltrials.gov (NCT05882214). We conducted the trial in compliance with guidelines of the International Conference on Harmonization Good Clinical Practice (ICH-GCP) and Medical Ethics Committee of Zhejiang Chinese Medical University.
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Li, J., Pan, K., Zhang, Y. et al. Dynamic evaluation of blood marker changes induced by acute binge drinking in healthy individuals: a randomized controlled trial. Sci Rep (2026). https://doi.org/10.1038/s41598-026-40028-1
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DOI: https://doi.org/10.1038/s41598-026-40028-1