Department of Medicine, University of Eastern Finland, Kuopio University Hospital, 70210, Kuopio, Finland.
Diabetologia. 2011 Mar;54(3):563-71. doi: 10.1007/s00125-010-1977-4. Epub 2010 Dec 12.
AIMS/HYPOTHESIS: Of the confirmed type 2 diabetes susceptibility loci only a few are known to affect insulin sensitivity. We examined the association of indices of hepatic and adipocyte insulin resistance (IR) with 19 confirmed type 2 diabetes risk loci in a large population-based study.
Non-diabetic participants (n = 8,460, age 57.3 ± 7.0 years, BMI 26.8 ± 3.8 kg/m(2); mean ± SD) from a population-based cohort underwent an OGTT. Of them, 6,733 non-diabetic men were genotyped for single nucleotide polymorphisms (SNPs) in or near PPARG2 (also known as PPARG), KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2B, IGF2BP2, CDKAL1, HNF1B, WFS1, JAZF1, CDC123, TSPAN8, THADA, ADAMTS9, NOTCH2, KCNQ1, MTNR1B and SNP rs7480010. We investigated hepatic IR with a new index of liver IR. The adipocyte IR index was defined as a product of fasting NEFA and plasma insulin levels.
Type 2 diabetes risk SNPs in or near KCNJ11 and HHEX were significantly (p < 0.0013), and those in or near CDKN2B, NOTCH2 and MTNR1B were nominally (p < 0.05), associated with decreased liver IR index. The Pro12 allele of PPARG2 was significantly associated with a high adipocyte IR index and nominally associated with high liver IR.
CONCLUSIONS/INTERPRETATION: The Pro12 allele of PPARG2 seems to impair insulin's antilipolytic effect, leading to high NEFA release in the fasting state and IR. In addition, the type 2 diabetes risk alleles of KCNJ11 and HHEX, which are known to impair insulin secretion, were associated with increased hepatic insulin sensitivity.
目的/假设:在已确认的 2 型糖尿病易感基因座中,只有少数几个已知会影响胰岛素敏感性。我们在一项大型基于人群的研究中,检查了肝脏和脂肪细胞胰岛素抵抗(IR)指数与 19 个已确认的 2 型糖尿病风险基因座之间的关联。
一项基于人群的队列中的非糖尿病参与者(n=8460,年龄 57.3±7.0 岁,BMI 26.8±3.8kg/m2;平均值±标准差)接受了口服葡萄糖耐量试验。其中,6733 名非糖尿病男性对位于或附近的单核苷酸多态性(SNP)进行了基因分型PPARG2(也称为 PPARG)、KCNJ11、TCF7L2、SLC30A8、HHEX、CDKN2B、IGF2BP2、CDKAL1、HNF1B、WFS1、JAZF1、CDC123、TSPAN8、THADA、ADAMTS9、NOTCH2、KCNQ1、MTNR1B 和 SNP rs7480010。我们用新的肝脏 IR 指数来研究肝脏 IR。脂肪细胞 IR 指数定义为空腹 NEFA 和血浆胰岛素水平的乘积。
位于或附近 KCNJ11 和 HHEX 的 2 型糖尿病风险 SNP 显著(p<0.0013),位于或附近 CDKN2B、NOTCH2 和 MTNR1B 的 SNP 显著(p<0.05)与肝脏 IR 指数降低相关。PPARG2 的 Pro12 等位基因与高脂肪细胞 IR 指数显著相关,与高肝脏 IR 指数显著相关。
结论/解释:PPARG2 的 Pro12 等位基因似乎会损害胰岛素的抗脂肪分解作用,导致空腹状态下 NEFA 的释放增加和 IR。此外,已知会损害胰岛素分泌的 KCNJ11 和 HHEX 的 2 型糖尿病风险等位基因与肝脏胰岛素敏感性增加有关。