Genetics of type 1 diabetes: similarities and differences between Asian and Caucasian populations

Ann N Y Acad Sci. 2006 Oct:1079:51-9. doi: 10.1196/annals.1375.008.

Abstract

Transracial studies are a powerful tool for genetic association studies of multifactorial diseases, such as type 1 diabetes. We therefore studied the association of candidate genes, HLA, INS, CTLA4, PTPN22, and SUMO4, with type 1 diabetes in Asian populations in comparison with Caucasian populations. Class II HLA was strongly associated with type 1 diabetes in both Asian and Caucasian populations, but alleles associated with type 1 diabetes are different among different ethnic groups due to difference in allele distribution in general populations. INS was associated with type 1 diabetes in both Japanese and Caucasian populations, but frequency of disease-associated haplotype was markedly higher in Japanese than in Caucasian populations. CTLA4 association was reported for both type 1 diabetes and autoimmune thyroid diseases (AITD) in Caucasian populations, but the association with type 1 diabetes was concentrated in a subset of patients with AITD in Japanese. A variant (R620W) of PTPN22 was consistently associated with type 1 diabetes in Caucasian populations, but the variant was absent in Asian populations including Japanese. M55V variant of SUMO4 was significantly associated with type 1 diabetes in Asians, but genetic heterogeneity between Asian and Caucasian populations was suggested. These data indicate the importance of transracial studies with a large number of samples in each ethnic group in genetic dissection of type 1 diabetes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alleles
  • Asian People / genetics*
  • Autoimmune Diseases / genetics*
  • Diabetes Mellitus, Type 1 / genetics*
  • Diabetes Mellitus, Type 1 / immunology
  • Gene Frequency
  • Genetic Heterogeneity
  • Haplotypes
  • Histocompatibility Antigens Class II / genetics
  • Humans
  • Japan / epidemiology
  • Population / genetics*
  • Small Ubiquitin-Related Modifier Proteins / genetics
  • Thyroiditis, Autoimmune / genetics
  • White People / genetics*

Substances

  • Histocompatibility Antigens Class II
  • Small Ubiquitin-Related Modifier Proteins