Buzzetti Raffaella, Petrone Antonio, Ribaudo Maria Cristina, Alemanno Irene, Zavarella Sara, Mein Charles A, Maiani Francesca, Tiberti Claudio, Baroni Marco Giorgio, Vecci Elio, Arca Marcello, Leonetti Frida, Di Mario Umberto
Endocrinology, Department of Clinical Sciences, University of Rome La Sapienza, Rome, Italy. raffaella.buzzetti@uniroma1@it
Eur J Hum Genet. 2004 Dec;12(12):1050-4. doi: 10.1038/sj.ejhg.5201283.
Several genetic variants of peroxisome proliferator-activated receptor-gamma2 (PPAR-gamma2) have been identified, among which Pro12Ala, a missense mutation in exon 2, is highly prevalent in Caucasian populations. Up to now, conflicting results with regard to the association between this mutation and complex traits, such as obesity, insulin sensitivity and Type 2 diabetes, have been reported. We investigated the influence of the Pro12Ala polymorphism of PPAR-gamma2 on insulin sensitivity in a large Italian population sample, n=1215, in whom extensive clinical and biochemical analyses were performed. To estimate the insulin sensitivity status, the homeostasis model assessment of insulin resistance (HOMA-IR) was calculated; in the obese/overweight subjects an oral glucose tolerance test (OGTT) was also performed and the Matsuda insulin sensitivity index (ISI) calculated. The insulin secretion index (homeostasis model assessment of percent beta-cell function, HOMA-beta%) was utilized to evaluate beta-cell function. The effect of the Pro12Ala polymorphism on quantitative variables was tested using multiple linear regression analysis. X12Ala (either Pro12Ala or Ala12Ala) genotype was associated with significantly lower fasting insulin levels compared to Pro/Pro (P=0.01 after correction for multiple comparisons) in all subjects. Consistent with this finding, significantly lower HOMA-IR was observed in X12Ala carriers (P=0.013 after correction for multiple comparisons) in all cohort. Moreover, no significant interaction effect was observed between body mass index and X12Ala polymorphism and between gender and X12Ala polymorphism in modulating insulin sensitivity. Our observations substantially extend previous findings and demonstrated that X12Ala variant is significantly associated with greater insulin sensitivity.
已鉴定出过氧化物酶体增殖物激活受体γ2(PPAR-γ2)的几种基因变体,其中外显子2中的错义突变Pro12Ala在白种人群中非常普遍。到目前为止,关于这种突变与肥胖、胰岛素敏感性和2型糖尿病等复杂性状之间关联的结果相互矛盾。我们在一个n = 1215的意大利大样本人群中研究了PPAR-γ2的Pro12Ala多态性对胰岛素敏感性的影响,对这些人群进行了广泛的临床和生化分析。为了评估胰岛素敏感性状态,计算了胰岛素抵抗的稳态模型评估(HOMA-IR);在肥胖/超重受试者中还进行了口服葡萄糖耐量试验(OGTT)并计算了松田胰岛素敏感性指数(ISI)。利用胰岛素分泌指数(β细胞功能百分比的稳态模型评估,HOMA-β%)来评估β细胞功能。使用多元线性回归分析测试Pro12Ala多态性对定量变量的影响。在所有受试者中,与Pro/Pro相比,X12Ala(Pro12Ala或Ala12Ala)基因型与显著更低的空腹胰岛素水平相关(多重比较校正后P = 0.01)。与这一发现一致,在所有队列中,X12Ala携带者的HOMA-IR显著更低(多重比较校正后P = 0.013)。此外,在调节胰岛素敏感性方面,未观察到体重指数与X12Ala多态性之间以及性别与X12Ala多态性之间有显著的交互作用。我们的观察结果极大地扩展了先前的发现,并证明X12Ala变体与更高的胰岛素敏感性显著相关。