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.

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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

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article

A genome-wide study of the effect of alcohol consumption on the risk of type 2 diabetes

Marie‐Christyne Cyr, Marie‐Pierre Dubé, Sylvie Provost, Sam Pedro Galilée Ayivi et al.
Clinical Nutrition Open Science
Alcohol Consumption and Health Effects
article

A genome-wide study of the effect of alcohol consumption on the risk of type 2 diabetes

Marie‐Christyne Cyr, Marie‐Pierre Dubé, Sylvie Provost, Sam Pedro Galilée Ayivi, Louis‐Philippe Lemieux Perreault, Ariane Belzile, Géraldine Asselin
article en

Abstract

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.

Clinical Nutrition Open ScienceVol. 60
Montreal Heart Institute (CA), Université de Montréal (CA)
Fondation Institut de Cardiologie de Montréal
Good health and well-being
Openalex Percentile: Top 97%
Alcohol Consumption and Health Effects
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