Zhang Dongying, Ma Jun, Brismar Kerstin, Efendic Suad, Gu Harvest F
Department of Molecular Medicine and Surgery, Rolf Luft Center for Diabetes Research, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
J Diabetes Complications. 2009 Jul-Aug;23(4):265-72. doi: 10.1016/j.jdiacomp.2008.05.004. Epub 2008 Jul 3.
The adiponectin promoter single nucleotide polymorphism (SNP) -11391G/A is found to be associated with nephropathy in type 1 diabetic (T1D) patients among Danish, but not French, Finnish, and Swedish populations. In the present study, we identified the binding sites for transcriptional factors in the adiponectin promoter region and also evaluated the association between adiponectin promoter polymorphisms and diabetic nephropathy (DN) in T1D patients.
Three adiponectin promoter SNPs, including -11377C/G, -11391G/A, and -11426A/G, were genotyped with dynamic allele-specific hybridization. The subjects included 1177 American T1D patients (622 females/555 males) with or without DN. All patients are of European descent and selected from the Genetics of Kidneys in Diabetes (GoKinD) study.
We identified four binding sites of transcriptional stimulatory protein (SP1) in the adiponectin putative promoter and found that the G allele of SNP -11377C/G altered the sequence for one of the SP1 binding sites. This polymorphism was significantly associated with DN in female T1D patients (P=.022, OR=1.352, 95% CI=1.044-1.752). Further analyses indicated the common diplotype (haplotypic genotype) H1/H1, constructed with SNPs -11377C/G and -11391G/A, was significantly associated with DN in females (P=.013), while the association of another diplotype H1/H2 with DN in females was of borderline significance (P=.071).
The present study thus provides the first evidence that SNP -11377C/G alters the sequence in one of the SP1 binding sites in the adiponectin promoter region. This polymorphism, together with another promoter SNP -11391G/A, may confer susceptibility to the development of DN in T1D patients among the GoKinD population.
已发现脂联素启动子单核苷酸多态性(SNP)-11391G/A与丹麦1型糖尿病(T1D)患者的肾病相关,但在法国、芬兰和瑞典人群中并非如此。在本研究中,我们确定了脂联素启动子区域转录因子的结合位点,并评估了脂联素启动子多态性与T1D患者糖尿病肾病(DN)之间的关联。
采用动态等位基因特异性杂交对三个脂联素启动子SNP进行基因分型,包括-11377C/G、-11391G/A和-11426A/G。研究对象包括1177例患有或未患有DN的美国T1D患者(622例女性/555例男性)。所有患者均为欧洲血统,选自糖尿病肾脏遗传学(GoKinD)研究。
我们在脂联素假定启动子中确定了转录刺激蛋白(SP1)的四个结合位点,发现SNP -11377C/G的G等位基因改变了其中一个SP1结合位点的序列。这种多态性与女性T1D患者的DN显著相关(P = 0.022,OR = 1.352,95%CI = 1.044 - 1.752)。进一步分析表明,由SNP -11377C/G和-11391G/A构建的常见双倍型(单倍型基因型)H1/H1与女性DN显著相关(P = 0.013),而另一种双倍型H1/H2与女性DN的关联具有临界显著性(P = 0.071)。
本研究因此首次提供了证据,证明SNP -11377C/G改变了脂联素启动子区域中一个SP1结合位点的序列。在GoKinD人群中,这种多态性与另一个启动子SNP -11391G/A可能会使T1D患者易患DN。