Genetic Epidemiology of Diabetic Complications

在目前的项目中，正在使用遗传连锁和关联分析技术寻找糖尿病肾病和相关性状的遗传决定因素。淋巴母细胞系已经从信息性系谱中建立起来。从流行病学研究中获得的血液标本中提取的核粒中可获得其他科的DNA。利用遗传连锁和关联方法进行的图谱研究，正被用于确定包含赋予糖尿病肾病易感性和相关特征的变异的基因组区域。通过与多中心肾病家族调查（FIND）联盟的合作，糖尿病肾病和糖尿病视网膜病变的遗传学也正在研究中。FIND是作为一项全基因组连锁研究而启动的，目前正在使用全基因组关联策略来确定感兴趣的区域。

In the current project, genetic determinants of diabetic nephropathy and related traits are being sought using techniques of genetic linkage and association analysis. Lymphoblast cell lines have been established from informative pedigrees. DNA is available from other families in nuclear pellets extracted from blood specimens obtained in the epidemiologic studies. Mapping studies, using both genetic linkage and association methods, are being used to identify genomic regions containing variants that confer susceptibility to diabetic kidney disease and related traits. Through collaboration with the multicenter Family Investigation of Nephropathy (FIND) consortium, the genetics of diabetic nephropathy and of diabetic retinopathy are also being studied. FIND was initiated as a genome-wide linkage study and is currently using a genome-wide association strategy to identify regions of interest. A genome-wide association study for diabetic nephropathy using 1,000,000 single nucleotide polymorphisms has also been conducted part of the FIND consortium. Initial analyses showed several regions that potentially harbor nephropathy-susceptibility loci. Replication studies in additional samples identified a variant between CNKSR3 and SCAF8 that was associated with nephropathy at genome-wide statistical significance, and across multiple ethnic groups. Recent studies have found that low-frequency variants identified as associated with renal function measures in Hispanic populations had similar frequencies in Indigenous Americans but did not replicate as associated with kidney function. Additional follow-up analyses are currently underway. Current efforts are focused on analysis of genome-wide association in the full collection of samples from the FIND consortium; further genome-wide association studies are being conducted in American Indian studies. With collaborators, dense linkage disequilibrium maps are being generated in candidate regions for linkage with nephropathy and total cholesterol in American Indian. We found that some DNA methylation profiles from peripheral blood observed in East Asians are also predictive in American Indians; further analyses of DNA methylation profiles and replication studies of this are being pursued. Additional Indigenous families informative for association studies of diabetic nephropathy continue to be recruited. In conjunction with collaborators, additional families informative for study of genetics of diabetic nephropathy have been recruited in Micronesia, and genotyping is underway for a genome-wide association study. Genotyping of additional individuals is planned for replication.