Department of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
Sportology Center, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
J Clin Endocrinol Metab. 2021 Aug 18;106(9):e3573-e3581. doi: 10.1210/clinem/dgab324.
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.
To investigate the association between ALDH2 rs671 and metabolic characteristics.
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 1H-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).
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·m-2·min-1 vs 0.87 ± 0.09 dL·m-2·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.
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.
最近一项针对东亚人群全基因组关联研究数据的荟萃分析发现,乙醛脱氢酶 2(ALDH2)rs671 是男性 2 型糖尿病的易感变异。
探讨 ALDH2 rs671 与代谢特征的关系。
我们研究了 94 名非肥胖、非糖尿病的日本男性。通过两步高胰岛素-正常血糖钳夹试验,我们评估了肌肉和肝脏的胰岛素敏感性。使用 1H 磁共振波谱和磁共振成像分别测量肝内脂质和脂肪分布。我们将参与者分为携带 ALDH2 rs671 G/G 的风险组(n=53)和不携带 ALDH2 rs671 G/A 或 A/A 的非风险组(n=41)。
风险组的饮酒量明显较高(18.4 [四分位距,IQR,10.4-48.9] vs 12.1 [IQR,1.3-29.0] g/天;P=0.003),空腹血糖(FPG)升高(97.5±7.9 vs 93.5±6.2 mg/dL;P=0.010),肝胰岛素敏感性降低(61.7±20.5% vs 73.1±15.9%;P=0.003),空腹血糖清除率降低(0.84±0.8 dL·m-2·min-1 vs 0.87±0.09 dL·m-2·min-1;P=0.047),而非风险组。而肌肉胰岛素抵抗和体脂肪分布相似。单一线性相关分析显示,饮酒量与肝胰岛素敏感性(r=-0.262,P=0.011)、空腹血糖清除率(r=-0.370,P<0.001)或 FPG(r=0.489,P<0.001)呈显著相关。多元回归分析显示,ALDH2 rs671 G/G 基因型和饮酒量均为肝胰岛素敏感性的显著独立相关因素,而只有饮酒量是空腹血糖清除率的显著独立相关因素。
我们的数据表明,由于高饮酒量导致的高酒精摄入依赖性和非依赖性肝胰岛素抵抗以及空腹血糖清除率降低可能是 ALDH2 rs671 G/G 携带者中相对上游的代谢异常。