The association between the FTO gene variant and alcohol consumption and binge and problem drinking in different gene-environment background: The HAPIEE study
Language English Country Netherlands Media print-electronic
Document type Journal Article
Grant support
FS/18/23/33512
British Heart Foundation - United Kingdom
PubMed
31055022
DOI
10.1016/j.gene.2019.05.002
PII: S0378-1119(19)30457-3
Knihovny.cz E-resources
- Keywords
- ADH1B, Alcohol intake, Binge drinking, FTO, Polymorphism, Sex, Smoking,
- MeSH
- Alcohol Dehydrogenase genetics MeSH
- Alcoholism genetics MeSH
- White People genetics MeSH
- Alpha-Ketoglutarate-Dependent Dioxygenase FTO genetics MeSH
- Genetic Association Studies MeSH
- Genotype MeSH
- Gene-Environment Interaction MeSH
- Polymorphism, Single Nucleotide * MeSH
- Smoking genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Binge Drinking genetics MeSH
- Alcohol Drinking genetics MeSH
- Prospective Studies MeSH
- Aged MeSH
- Sex Factors MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- ADH1B protein, human MeSH Browser
- Alcohol Dehydrogenase MeSH
- FTO protein, human MeSH Browser
- Alpha-Ketoglutarate-Dependent Dioxygenase FTO MeSH
BACKGROUND: Alcohol intake and tobacco smoking have significant negative health consequences and both are influenced by genetic predispositions. Some studies suggest that the FTO gene is associated with alcohol consumption. We investigated whether a tagging variant (rs17817449) within the FTO gene is associated with alcohol intake, problem drinking and smoking behaviour. METHODS: We analysed data from 26,792 Caucasian adults (47.2% of males; mean age 58.9 (±7.3) years), examined through the prospective cohort HAPIEE study. The primary outcomes were daily alcohol consumption, binge drinking, problem drinking (CAGE score 2+) and smoking status in relation to tagging variants within the FTO and ADH1B genes. RESULTS: We found no significant association of the FTO polymorphism with smoking status in either sex. The associations of the FTO polymorphism with drinking pattern were inconsistent and differed by gender. In men, GG homozygote carriers had lower odds of problem drinking (OR 0.85, 95% CI 0.75-0.96, p = 0.03). In women, the combination of the FTO/ADH1B GG/+A genotypes doubled the risk of binge drinking (OR 2.10, 95% CI 1.19-3.71, p < 0.05), and the risk was further increased among smoking women (OR 4.10, 95% CI 1.64-10.24, p = 0.008). CONCLUSIONS: In this large population study, the FTO gene appeared associated with binge and problem drinking, and the associations were modified by sex, smoking status and the ADH1B polymorphism.
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