Gjesing A P, Andersen G, Borch-Johnsen K, Jørgensen T, Hansen T, Pedersen O
Steno Diabetes Center, Niels Steensens Vej 1, NLC2.12, DK-2820 Gentofte, Denmark.
Mol Genet Metab. 2008 May;94(1):90-7. doi: 10.1016/j.ymgme.2007.12.003. Epub 2008 Jan 14.
AIM/HYPOTHESIS: The functional variant Trp64Arg in the beta(3)-adrenergic receptor has previously been examined for association with obesity and insulin resistance with ambiguous results. For further evaluation the present study examined the impact of the Trp64Arg variant on the pathogenesis of type 2 diabetes and obesity in a relatively large, homogenous study population.
The Trp64Arg polymorphism was genotyped in 7605 Danish subjects using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Association was examined in case-control studies of obesity (1529 cases and 6049 controls) and type 2 diabetes (1373 cases and 4742 controls) and quantitative trait analyses among 5822 individuals. Furthermore, the association of Trp64Arg with type 2 diabetes was examined in a meta-analysis.
The Trp64Arg polymorphism was not associated with obesity. However, the Arg-allele was associated with a slightly increased risk of type 2 diabetes (OR1.15 (CI: 1.01-1.31); p=0.04), increased insulin resistance estimated by homeostasis model assessment (p=0.01), higher fasting serum insulin levels (p=0.01), and higher levels of plasma glucose 2-h after glucose ingestion (p=0.02). After sex stratification these associations were only present among women. Furthermore, the Arg-allele was borderline associated with type 2 diabetes in a meta-analysis of the present and 26 previous studies (p=0.06, OR1.27 (CI: 0.99-1.63)) (n=18891).
CONCLUSION/INTERPRETATION: Trp64Arg does not confer an increased risk of obesity among Danes. Yet, in the present study of 7605 Danes the variant is associated with type 2 diabetes and quantitative traits related to type 2 diabetes.
目的/假设:先前已对β(3)-肾上腺素能受体中的功能性变体色氨酸64精氨酸(Trp64Arg)与肥胖症和胰岛素抵抗的关联性进行了研究,但结果并不明确。为了进一步评估,本研究在一个相对较大的同质研究人群中,考察了Trp64Arg变体对2型糖尿病和肥胖症发病机制的影响。
采用基质辅助激光解吸/电离飞行时间质谱法,对7605名丹麦受试者的Trp64Arg多态性进行基因分型。在肥胖症(1529例病例和6049例对照)和2型糖尿病(1373例病例和4742例对照)的病例对照研究中,以及在5822名个体中进行数量性状分析,以检验关联性。此外,还通过荟萃分析考察了Trp64Arg与2型糖尿病的关联性。
Trp64Arg多态性与肥胖症无关。然而,精氨酸等位基因与2型糖尿病风险略有增加相关(比值比1.15(置信区间:1.01 - 1.31);p = 0.04),通过稳态模型评估得出的胰岛素抵抗增加(p = 0.01),空腹血清胰岛素水平较高(p = 0.01),以及葡萄糖摄入后2小时血浆葡萄糖水平较高(p = 0.02)。按性别分层后,这些关联性仅在女性中存在。此外,在对本研究和之前26项研究的荟萃分析中,精氨酸等位基因与2型糖尿病存在临界关联性(p = 0.06,比值比1.27(置信区间:0.99 - 1.63))(n = 18891)。
结论/解读:Trp64Arg不会增加丹麦人患肥胖症的风险。然而,在本项针对7605名丹麦人的研究中,该变体与2型糖尿病以及与2型糖尿病相关的数量性状有关。