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葡萄糖钳夹技术揭示了肥胖受试者脂联素基因多态性与胰岛素敏感性之间的关联。

The glucose clamp reveals an association between adiponectin gene polymorphisms and insulin sensitivity in obese subjects.

作者信息

Buzzetti R, Petrone A, Zavarella S, Zampetti S, Spoletini M, Potenziani S, Leto G, Osborn J, Leonetti F

机构信息

Endocrinology, Department of Clinical Sciences, Università di Roma La Sapienza, Viale del Policlinico 155, Rome, Italy.

出版信息

Int J Obes (Lond). 2007 Mar;31(3):424-8. doi: 10.1038/sj.ijo.0803419. Epub 2006 Jun 27.

Abstract

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.

摘要

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

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