Buzzetti R, Petrone A, Zavarella S, Zampetti S, Spoletini M, Potenziani S, Leto G, Osborn J, Leonetti F
Endocrinology, Department of Clinical Sciences, Università di Roma La Sapienza, Viale del Policlinico 155, Rome, Italy.
Int J Obes (Lond). 2007 Mar;31(3):424-8. doi: 10.1038/sj.ijo.0803419. Epub 2006 Jun 27.
Results concerning the association of adiponectin gene polymorphisms (single-nucleotide polymorphisms, SNPs) with obesity, type 2 diabetes (T2DM), metabolic disorders and insulin resistance have not lead to definite conclusions. The aim of our study was to investigate a possible association between the -11391G>A and -11377C>G SNPs of adiponectin gene and measure of insulin sensitivity evaluated by the hyperinsulinemic-euglycemic clamp in a group of 'uncomplicated' obese subjects (with no associated comorbidities) (n=99, mean age 35 years) with a history of obesity lasting at least 10 years. The study of uncomplicated obese subjects, free of possible confounding factors that could interfere with insulin sensitivity, such as pharmacological treatment, provides a good model to assess insulin sensitivity per se. We observed that subjects homozygous for the G allele at locus -11391 had lower M (mg/kg min)/fat-free mass (FFM) index and adiponectin levels compared to subjects with GA+AA genotypes (P=0.002 and P=0.03, respectively) and subjects carrying the -11377G variant had lower M (mg/kg min)/FFM index and adiponectin levels compared to noncarriers (P=0.003 and P=0.03, respectively). Our results imply that the two promoter SNPs, -11391G>A and -11377C>G, of the adiponectin gene are associated with a reduced insulin sensitivity evaluated by hyperinsulinemic-euglycemic clamp in obese subjects.
脂联素基因多态性(单核苷酸多态性,SNPs)与肥胖、2型糖尿病(T2DM)、代谢紊乱及胰岛素抵抗之间关联的研究结果尚未得出明确结论。我们研究的目的是在一组“无并发症”的肥胖受试者(无相关合并症)(n = 99,平均年龄35岁,肥胖病史至少10年)中,研究脂联素基因的 -11391G>A和 -11377C>G SNPs与通过高胰岛素-正常血糖钳夹评估的胰岛素敏感性之间的可能关联。对无可能干扰胰岛素敏感性的混杂因素(如药物治疗)的单纯肥胖受试者进行研究,为评估胰岛素敏感性本身提供了一个良好模型。我们观察到,与GA + AA基因型受试者相比,-11391位点G等位基因纯合的受试者的M(mg/kg·min)/去脂体重(FFM)指数和脂联素水平较低(分别为P = 0.002和P = 0.03),与非携带者相比,携带 -11377G变异的受试者的M(mg/kg·min)/FFM指数和脂联素水平较低(分别为P = 0.003和P = 0.03)。我们的结果表明,脂联素基因的两个启动子SNPs,即 -11391G>A和 -11377C>G,与肥胖受试者通过高胰岛素-正常血糖钳夹评估的胰岛素敏感性降低有关