Department of Neuroscience, Functional pharmacology, Uppsala University, Uppsala, Sweden.
Int J Obes (Lond). 2012 Jan;36(1):119-29. doi: 10.1038/ijo.2011.11. Epub 2011 Feb 8.
Recently a genome-wide association analysis from five European populations identified a polymorphism located downstream of the mannosyl-(α-1,3)-glycoprotein-β-1,2-N-acetylglucosaminyltransferase (MGAT1) gene that was associated with body-weight. In the present study, associations between MGAT1 variants combined with obesity and insulin measurements were investigated in three cohorts. Levels of fatty acids and estimated measures of Δ desaturases were also investigated among adult men.
Six polymorphisms downstream of MGAT1 were genotyped in a cross-sectional cohort of 1152 Swedish men. Three polymorphisms were further analyzed in a case-control study of 1076 Swedish children and in a cross-sectional study of 2249 Greek children.
Three polymorphisms, rs12186500 (odds ratio (OR): 1.892, 95% confidence interval (CI): 1.237-2.895, P=0.003), rs1021001 (OR: 2.102, 95% CI: 1.280-3.455, P=0.003) and rs4285184 (OR: 1.587, 95% CI: 1.024-2.459, P=0.038) were associated with a higher prevalence of obesity among the adult men and a trend for obesity was observed for rs4285184 among the Swedish (OR: 1.205, 95% CI: 0.987-1.471, P=0.067) and Greek children (OR: 1.192, 95%CI: 0.978-1.454, P=0.081). Association with body weight was observed for rs12186500 (P=0.017) and rs4285184 (P=0.024) among the men. The rs1021001 and rs4285184 were also associated with body mass index (BMI) in the two Swedish cohorts and similar trends were observed among the Greek children. The combined effect size for rs1021001 and rs4285184 on BMI z-score from a meta-analysis was 0.233 (95% CI:0.093-0.373, P=0.001) and 0.147 (95% CI:0.057-0.236, P=0.001), respectively. We further observed associations between the genetic variants and fatty acids (P<0.039) and estimated measures of Δ desaturases (P<0.040), as well as interactions for rs12186500 (P<0.019) with an effect on BMI. No association was found with homeostatic model assessment-insulin resistance in any cohort but increased insulin levels, insulin response and decreased insulin sensitivity were observed among the children (P<0.038).
Genetic variants downstream MGAT1 seem to influence susceptibility to obesity. Moreover, these genetic variants affect the levels of serum unsaturated fatty acids and Δ desaturase indices, variables previously shown to correlate with obesity.
最近,来自五个欧洲人群的全基因组关联分析确定了位于甘露糖基-(α-1,3)-糖蛋白-β-1,2-N-乙酰氨基葡萄糖基转移酶(MGAT1)基因下游的一个多态性与体重有关。在本研究中,在三个队列中研究了 MGAT1 变体与肥胖和胰岛素测量的组合关联。还在成年男性中研究了脂肪酸水平和估计的 Δ 去饱和酶测量值。
在 1152 名瑞典男性的横断面队列中对 MGAT1 下游的 6 个多态性进行了基因分型。进一步在 1076 名瑞典儿童的病例对照研究和 2249 名希腊儿童的横断面研究中分析了 3 个多态性。
三个多态性,rs12186500(比值比(OR):1.892,95%置信区间(CI):1.237-2.895,P=0.003),rs1021001(OR:2.102,95%CI:1.280-3.455,P=0.003)和 rs4285184(OR:1.587,95%CI:1.024-2.459,P=0.038)与成年男性肥胖患病率较高相关,并且 rs4285184 与瑞典(OR:1.205,95%CI:0.987-1.471,P=0.067)和希腊儿童(OR:1.192,95%CI:0.978-1.454,P=0.081)的肥胖趋势有关。在男性中,rs12186500(P=0.017)和 rs4285184(P=0.024)与体重相关。rs1021001 和 rs4285184 也与两个瑞典队列的体重指数(BMI)相关,并且在希腊儿童中也观察到类似的趋势。对 BMI z 评分的 rs1021001 和 rs4285184 的合并效应大小来自荟萃分析为 0.233(95%CI:0.093-0.373,P=0.001)和 0.147(95%CI:0.057-0.236,P=0.001),分别。我们还观察到遗传变异与脂肪酸(P<0.039)和估计的 Δ 去饱和酶(P<0.040)之间的关联,以及 rs12186500 与 BMI 的交互作用(P<0.019)。在任何队列中都没有发现与稳态模型评估胰岛素抵抗有关,但在儿童中观察到胰岛素水平升高、胰岛素反应和胰岛素敏感性降低(P<0.038)。
MGAT1 下游的遗传变异似乎会影响肥胖的易感性。此外,这些遗传变异会影响血清不饱和脂肪酸和 Δ 去饱和酶指数的水平,这些变量以前与肥胖有关。