Kilpeläinen T O, Lakka T A, Laaksonen D E, Laukkanen O, Lindström J, Eriksson J G, Valle T T, Hämäläinen H, Aunola S, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Tuomilehto J, Uusitupa M, Laakso M
Institute of Biomedicine, Physiology, University of Kuopio, Kuopio, Finland.
Physiol Genomics. 2007 Oct 22;31(2):264-72. doi: 10.1152/physiolgenomics.00036.2007. Epub 2007 Jul 17.
Single nucleotide polymorphisms (SNPs) in two genes regulating insulin secretion, SLC2A2 (encoding GLUT2) and ABCC8 (encoding SUR1), were associated with the conversion from impaired glucose tolerance (IGT) to type 2 diabetes (T2D) in the Finnish Diabetes Prevention Study (DPS). We determined whether physical activity (PA), assessed annually with a questionnaire, modified the association of SNPs in SLC2A2 and ABCC8 with the conversion to T2D in the combined intervention and control groups of the DPS. Finnish overweight subjects with IGT (N = 479) were followed for an average of 4.1 yr. The interaction of the SNPs with the change in PA on the conversion to T2D was assessed using Cox regression with adjustments for the other components of the intervention (dietary changes, weight reduction). The carriers of the common homozygous genotype of rs5393, rs5394, or rs5404 of SLC2A2 and rs3758947 of ABCC8 who were in the lower third of the change in moderate-to-vigorous PA during the follow-up had a 2.6- to 3.7-fold increased risk of developing T2D compared with the upper third, whereas the rare allele carriers seemed to be unresponsive to changes in moderate-to-vigorous PA (for the interaction of genotype with change in PA, P = 0.022-0.027 for the SNPs in SLC2A2, and P = 0.007 for rs3758947). We conclude that moderate-to-vigorous PA may modify the risk of developing T2D associated with genes regulating insulin secretion (SLC2A2, ABCC8) in persons with IGT.
在芬兰糖尿病预防研究(DPS)中,调节胰岛素分泌的两个基因SLC2A2(编码GLUT2)和ABCC8(编码SUR1)中的单核苷酸多态性(SNP)与糖耐量受损(IGT)向2型糖尿病(T2D)的转变有关。我们确定,通过问卷每年评估的体力活动(PA)是否改变了DPS联合干预组和对照组中SLC2A2和ABCC8基因的SNP与向T2D转变之间的关联。对479名患有IGT的芬兰超重受试者进行了平均4.1年的随访。使用Cox回归评估SNP与PA变化对向T2D转变的相互作用,并对干预的其他组成部分(饮食变化、体重减轻)进行调整。在随访期间,中度至剧烈PA变化处于下三分之一的SLC2A2基因rs5393、rs5394或rs5404以及ABCC8基因rs3758947的常见纯合基因型携带者发生T2D的风险比上三分之一者增加了2.6至3.7倍,而罕见等位基因携带者似乎对中度至剧烈PA的变化无反应(对于基因型与PA变化的相互作用,SLC2A2基因的SNP的P值为0.022至0.027,rs3758947的P值为0.007)。我们得出结论,中度至剧烈的PA可能会改变IGT患者中与调节胰岛素分泌的基因(SLC2A2、ABCC8)相关的T2D发病风险。