Maeda Shiro
Laboratory for Diabetic Nephropathy, SNP Research Center, The Institute of Physical and Chemical Research (RIKEN), 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan.
Diabetes Res Clin Pract. 2004 Dec;66 Suppl 1:S45-7. doi: 10.1016/j.diabres.2003.09.017.
That genetic factors contribute to the onset and progression of chronic diabetic complications is highly convincing, but the gene or genes conferring susceptibility to these diseases remain to be identified. To identify genetic elements that might confer susceptibility to diabetic nephropathy, we performed a genome-wide analysis of gene-based single nucleotide polymorphisms (SNPs) in a large cohort of Japanese diabetic patients. In case-control association studies, patients with type 2 diabetes were divided into two groups, one having retinopathy as well as overt nephropathy and the other (the control group) with diabetic retinopathy but with no signs of renal involvement. Genotyping of these patients at more than 80,000 SNP loci suggested several distinct regions to be good candidates for the susceptibility to diabetic nephropathy. The results indicated that genome-wide search using SNP as a genetic marker is useful to identify the gene(s) susceptible to common diseases such as diabetic nephropathy.
遗传因素促成慢性糖尿病并发症的发生和发展,这一点极具说服力,但赋予这些疾病易感性的一个或多个基因仍有待确定。为了识别可能赋予糖尿病肾病易感性的遗传因素,我们对一大群日本糖尿病患者进行了基于基因的单核苷酸多态性(SNP)全基因组分析。在病例对照关联研究中,2型糖尿病患者被分为两组,一组患有视网膜病变以及显性肾病,另一组(对照组)患有糖尿病视网膜病变但无肾脏受累迹象。对这些患者在80000多个SNP位点进行基因分型,结果表明有几个不同区域很可能是糖尿病肾病易感性的候选区域。结果表明,以SNP作为遗传标记进行全基因组搜索,有助于识别像糖尿病肾病这类常见疾病的易感基因。