| Literature DB >> 27303105 |
Guang Yin1, Mariko Naito1, Kenji Wakai1, Emi Morita1, Sayo Kawai1, Nobuyuki Hamajima1, Sadao Suzuki2, Yoshikuni Kita3, Toshiro Takezaki4, Keitaro Tanaka5, Makiko Morita6, Hirokazu Uemura7, Etsuko Ozaki8, Satoyo Hosono9, Haruo Mikami10, Michiaki Kubo11, Hideo Tanaka9.
Abstract
Associations between alcohol consumption and type 2 diabetes risk are inconsistent in epidemiologic studies. This study investigated the associations of ADH1B and ALDH2 polymorphisms with fasting blood glucose levels, and the impact of the associations of alcohol consumption with fasting blood glucose levels in Japanese individuals. This cross-sectional study included 907 men and 912 women, aged 35-69 years. The subjects were selected from among the Japan Multi-institutional Collaborative Cohort study across six areas of Japan. The ADH1B and ALDH2 polymorphisms were genotyped by Invader Assays. The ALDH2 Glu504Lys genotypes were associated with different levels of fasting blood glucose in men (P = 0.04). Mean fasting glucose level was positively associated with alcohol consumption in men with the ALDH2 504 Lys allele (P trend = 0.02), but not in men with the ALDH2 504Glu/Glu genotype (P trend = 0.45), resulting in no statistically significant interaction (P = 0.38). Alcohol consumption was associated with elevated fasting blood glucose levels compared with non-consumers in men (P trend = 0.002). The ADH1B Arg48His polymorphism was not associated with FBG levels overall or after stratification for alcohol consumption. These findings suggest that the ALDH2 polymorphism is associated with different levels of fasting blood glucose through alcohol consumption in Japanese men. The interaction of ALDH2 polymorphisms in the association between alcohol consumption and fasting blood glucose warrants further investigation.Entities:
Keywords: ADH1B and ALDH2 polymorphisms; alcohol consumption; fasting blood glucose; type 2 diabetes
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Year: 2016 PMID: 27303105 PMCID: PMC4885818
Source DB: PubMed Journal: Nagoya J Med Sci ISSN: 0027-7622 Impact factor: 1.131