The association between the FTO gene variant and alcohol consumption and binge and problem drinking in different gene-environment background: The HAPIEE study

被引:6
|
作者
Hubacek, Jaroslav A. [1 ]
Pikhart, Hynek [2 ]
Peasey, Anne [2 ]
Malyutina, Sofia [3 ]
Pajak, Andrzej [4 ]
Tamosiunas, Abdonas [5 ]
Voevoda, Mikhail [3 ]
Holmes, Michael V. [6 ]
Bobak, Martin [2 ]
机构
[1] Inst Clin & Expt Med, Ctr Expt Med, Prague, Czech Republic
[2] UCL, Dept Epidemiol & Publ Hlth, Int Inst Hlth & Soc, London, England
[3] RAS, SB, Branch Inst Cytol & Genet, Res Inst Internal & Prevent Med, Novosibirsk, Russia
[4] Jagiellonian Univ, Med Coll, Fac Hlth Care, Dept Epidemiol & Populat Studies,Inst Publ Hlth, Krakow, Poland
[5] Lithuanian Univ Hlth Sci, Inst Cardiol, Dept Populat Studies, Kaunas, Lithuania
[6] Oxford Univ Hosp, Oxford Biomed Res Ctr, Natl Inst Hlth Res, Oxford, England
基金
英国惠康基金;
关键词
FTO; Polymorphism; Alcohol intake; Binge drinking; ADH1B; Smoking; Sex; GENOME-WIDE ASSOCIATION; BODY-MASS INDEX; FAT MASS; OBESITY; RISK; POLYMORPHISM; CHILDHOOD; GENOTYPE; ENERGY; ADH1B;
D O I
10.1016/j.gene.2019.05.002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 F7'0 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.
引用
收藏
页码:30 / 35
页数:6
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