Dipartimento di Scienze per la Salute, Università del Molise, Campobasso, Italy.
J Endocrinol Invest. 2012 Jan;35(1):2-4. doi: 10.1007/BF03345413.
The insulin resistance (IR) is a major metabolic impairment in severe obesity, a multifactorial disease in which the importance of the effect of single nucleotide polymorphisms (SNP) associations in different rather than individual genes was established. The aim of this study was to test the predictive value of presence/absence of polymorphisms/ variants in β3-adrenergic receptor (ADRB3), uncoupling protein 1 (UCP1), peroxisome proliferator-activated receptor γ (PPARγ), and adiponectin (ADIPOQ) genes in diagnosing the IR in obesity.
We studied 112 (40 males, 72 females) severely obese (body mass index: 48.5±7.5 kg/m2) subjects recruited from the outpatient obesity clinic of Federico II University Hospital in Naples. Genomic DNA was extracted from peripheral leukocytes with a commercial kit. The gene polymorphisms Trp64Arg in ADRB3, -3826 A>G in UCP1, Pro12Ala in PPARγ, and c.268G>A, c.331T>C, and c.334C>T in ADIPOQ were characterized by TaqMan assay or by direct sequencing (ADIPOQ).
Our results demonstrate that -3826A>G UCP1 polymorphism is associated with IR in morbid obesity. Further, the lack of any polymorphisms, Trp64Arg in ADRB3 and/or -3826 A>G in UCP1 and/or Pro12Ala in PPARγ and/or c.268G>A, c.331T>C and c.334C>T in ADIPOQ, appears a useful prognostic factor (NPV=100%) toward the IR onset in these obese patients representing a further parameter for an earlier and appropriate therapy.
胰岛素抵抗(IR)是严重肥胖症的一种主要代谢障碍,这是一种多因素疾病,其中单个核苷酸多态性(SNP)关联在不同而非单个基因中的作用的重要性已经确定。本研究的目的是测试β3-肾上腺素能受体(ADRB3)、解偶联蛋白 1(UCP1)、过氧化物酶体增殖物激活受体γ(PPARγ)和脂联素(ADIPOQ)基因中存在/不存在多态性/变体对肥胖症中 IR 的预测价值。
我们研究了 112 名(40 名男性,72 名女性)严重肥胖症(体重指数:48.5±7.5kg/m2)患者,这些患者均来自那不勒斯 Federico II 大学医院的门诊肥胖症诊所。外周白细胞中的基因组 DNA 用商业试剂盒提取。通过 TaqMan 测定或直接测序(ADIPOQ)对 ADRB3 的 Trp64Arg、UCP1 的-3826 A>G、PPARγ 的 Pro12Ala 以及 ADIPOQ 的 c.268G>A、c.331T>C 和 c.334C>T 基因多态性进行了特征分析。
结果表明,UCP1 的-3826A>G 多态性与肥胖症的 IR 相关。此外,ADRB3 的 Trp64Arg 和/或 UCP1 的-3826 A>G 和/或 PPARγ 的 Pro12Ala 和/或 ADIPOQ 的 c.268G>A、c.331T>C 和 c.334C>T 缺失任何多态性是这些肥胖患者发生 IR 的有用预后因素(NPV=100%),是早期和适当治疗的进一步参数。