4.7 Article

ALDH2 rs671 Is Associated With Elevated FPG, Reduced Glucose Clearance and Hepatic Insulin Resistance in Japanese Men

期刊

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 106, 期 9, 页码 E3573-E3581

出版社

ENDOCRINE SOC
DOI: 10.1210/clinem/dgab324

关键词

ALDH2; fasting plasma glucose; hepatic insulin resistance; East Asian

资金

  1. High Technology Research Center Grant
  2. Strategic Research Foundation at Private Universities
  3. KAKENHI from the Ministry of Education, Culture, Sports, Science and Technology of Japan [23680069, 26282197, 17K19929]
  4. Japan Diabetes Foundation
  5. Suzuken Memorial Foundation
  6. Mitsukoshi Welfare Foundation
  7. Diabetes Masters Conference

向作者/读者索取更多资源

The study found that individuals carrying the ALDH2 rs671 G/G genotype had higher alcohol consumption, elevated fasting plasma glucose, lower hepatic insulin sensitivity, and reduced fasting glucose clearance compared to those carrying the non-risk alleles. These results suggest that high alcohol intake may lead to hepatic insulin resistance and reduced fasting glucose clearance in carriers of the ALDH2 rs671 G/G genotype.
Context A recent meta-analysis of genome-wide association studies data from East Asians identified aldehyde dehydrogenase 2 (ALDH2) rs671 as a susceptibility variant for type 2 diabetes in males. Objective To investigate the association between ALDH2 rs671 and metabolic characteristics. Methods We studied 94 nonobese, nondiabetic, Japanese men. Using a 2-step hyperinsulinemic-euglycemic clamp, we evaluated insulin sensitivity in muscle and liver. Intrahepatic lipid and fat distribution were measured using H-1-magnetic resonance spectroscopy and magnetic resonance imaging, respectively. We divided participants into a risk-carrying group with ALDH2 rs671 G/G (n = 53) and a nonrisk-carrying group with ALDH2 rs671 G/A or A/A (n = 41). Results The risk-carrying group had significantly higher levels of alcohol consumption (18.4 [interquartile range, IQR, 10.4-48.9]) vs 12.1 (IQR, 1.3-29.0) g/day; P = .003), elevated fasting plasma glucose (FPG) (97.5 +/- 7.9 vs 93.5 +/- 6.2 mg/dL; P = .010), lower hepatic insulin sensitivity (61.7 +/- 20.5% vs 73.1 +/- 15.9%; P = .003), and lower fasting glucose clearance (0.84 +/- 0.8 dL center dot m(-2)center dot min(-1) vs 0.87 +/- 0.09 dL center dot m(-2)center dot min(-1); P = .047) than the nonrisk-carrying group, while insulin resistance in muscle and body fat distribution were similar. The single linear correlation analysis revealed significant correlations between alcohol consumption and hepatic insulin sensitivity (r = -0.262, P = .011), fasting glucose clearance (r = -0.370, P < .001), or FPG (r = 0.489, P < .001). The multiple regression analysis revealed that both ALDH2 rs671 G/G genotype and alcohol consumption were significant independent correlates for hepatic insulin sensitivity, whereas only alcohol consumption was a significant independent correlate for fasting glucose clearance. Conclusion Our data suggest that high-alcohol intake-dependent and independent hepatic insulin resistance and reduced fasting glucose clearance due to high alcohol intake could be a relatively upstream metabolic abnormality in ALDH2 rs671 G/G carriers.

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