A genome-wide study of the effect of alcohol consumption on the risk of type 2 diabetes
The relationship between alcohol consumption and type 2 diabetes risk is often described as a J- or U-shaped curve, with moderate drinkers having a lower risk compared to non-drinkers and heavy drinkers. However, this protective effect appears to be more pronounced in women than in men, suggesting a potential interaction between sex-specific factors and alcohol metabolism. We conducted an interaction genome-wide association study (GWAS) to identify genetic variants that modify the relationship between alcohol consumption and type 2 diabetes risk in a sex-specific manner. We utilized data from the UK Biobank in a case-control approach including 309,568 individuals to investigate the three-way interaction between genetic variants, alcohol consumption, and sex on type 2 diabetes risk. We identified genetic variant rs78681203, located between the FOXO6 and EDN2 genes, with a significant sex-specific interaction with alcohol consumption (interaction p = 2.85 × 10 −8 ). The T allele of rs78681203 was associated with an increased risk of type 2 diabetes in women consuming 0 to <4 UK units/week (OR = 1.19, 95% CI: 1.07–1.34) but had a protective effect in women consuming 4 to <28 UK units/week (OR = 0.81, 95% CI: 0.69–0.95). Conversely, in men, the T allele was associated with a higher risk of type 2 diabetes in the 4 to <28 UK units/week group (OR = 1.19, 95% CI: 1.08–1.32) and had a protective effect in the 0 to <4 UK units/week group (OR = 0.85, 95% CI: 0.74–0.99). Our findings suggest that genetic variation may play a role in the differential effects of alcohol consumption on type 2 diabetes risk between men and women. Further replication and mechanistic studies are needed to confirm and clarify the role of the identified genetic variant. • Genetic variant rs78681203 interacts with alcohol consumption on sex-specific type 2 diabetes risk. • The T allele of rs78681203 protects women with higher alcohol intake from type 2 diabetes but increases risk in men. • rs78681203 is located between FOXO6 and EDN2, genes linked to glucose homeostasis and vascular function, respectively. • Genetic variation can help clarify alcohol’s differing effects on type 2 diabetes risk in men and women.
Authors
- Marie‐Christyne Cyr (ORCID: https://orcid.org/0009-0001-1727-4740)
- Marie‐Pierre Dubé (ORCID: https://orcid.org/0000-0001-8442-4393)
- Sylvie Provost (ORCID: https://orcid.org/0000-0003-3133-0080)
- Sam Pedro Galilée Ayivi (ORCID: https://orcid.org/0000-0003-1975-6281)
- Louis‐Philippe Lemieux Perreault (ORCID: https://orcid.org/0000-0001-7423-0958)
- Ariane Belzile
- Géraldine Asselin (ORCID: https://orcid.org/0000-0002-3702-2962)
Institutions
- Montreal Heart Institute (CA)
- Université de Montréal (CA)
Publication Details
- Journal
- Clinical Nutrition Open Science
- Published
- 2025-02-03
- DOI
- https://doi.org/10.1016/j.nutos.2025.02.001
- Primary Topic
- Alcohol Consumption and Health Effects
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Fondation Institut de Cardiologie de Montréal