A novel single nucleotide polymorphism in the protein tyrosine phosphatase N22 gene (PTPN22) is associated with Type 1 diabetes in a Chinese population

Aims To examine single nucleotide polymorphisms in the protein tyrosine phosphatase N22 gene (PTPN22) and to study their association with Type 1 diabetes in a Chinese cohort. Methods Three hundred and sixty‐four young patients with Type 1 diabetes and 719 healthy children were included in this case‐...

Full description

Saved in:
Bibliographic Details
Published inDiabetic medicine Vol. 31; no. 2; pp. 219 - 226
Main Authors Pei, Z., Chen, X., Sun, C., Du, H., Wei, H., Song, W., Yang, Y., Zhang, M., Lu, W., Cheng, R., Luo, F.
Format Journal Article
LanguageEnglish
Published Oxford Blackwell Publishing Ltd 01.02.2014
Blackwell
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Aims To examine single nucleotide polymorphisms in the protein tyrosine phosphatase N22 gene (PTPN22) and to study their association with Type 1 diabetes in a Chinese cohort. Methods Three hundred and sixty‐four young patients with Type 1 diabetes and 719 healthy children were included in this case‐controlled study. The genotypes of rs1217385, rs2488457 (–1123C>G), rs1217414, rs1217419, rs3765598 and rs2476601 (1858C>T) in the PTPN22 gene were determined using the SNaPshot method. Alleles, genotypes and haplotype frequencies were compared between patients with Type 1 diabetes and healthy control subjects. The association between single nucleotide polymorphisms and clinical traits/autoantibody status was also analysed. Results The single nucleotide polymorphism, rs1217419, located in the second intron of the PTPN22 gene was associated with Type 1 diabetes (odds ratio 1.5, 95% CI 1.14–1.97, P = 0.003). An additional single nucleotide polymorphism, rs1217385, was also associated with Type 1 diabetes; however, the association was secondary to that of rs1217419. The previously reported single nucleotide polymorphism that is associated with Type 1 diabetes (–1123G>C) had only marginal association with Type 1 diabetes in our study. A marginal association was also identified between –1123G>C and glutamic acid decarboxylase autoantibody positivity in patients with Type 1 diabetes. There was no association between the single nucleotide polymorphism 1858C>T and Type 1 diabetes in our studied cohort. Conclusions Our study confirmed that PTPN22 is a gene that contributes to Type 1 diabetes susceptibility. The primary association occurs with single nucleotide polymorphism rs1217419 and there is clear heterogeneity of the association between PTPTN22 polymorphisms and Type 1 diabetes in a Chinese population compared with other populations. What's new? Our cohort is the largest Chinese cohort studied to date in this research field. A novel Type 1 diabetes‐associated single nucleotide polymorphism in the protein tyrosine phosphatase N22 gene (PTPN22) was identified. Our analysis clearly showed ethnic differences in PTPN22–Type 1 diabetes association compared with other populations.
Bibliography:istex:D2FBF103DE7D1CD54535ABE2B409BD1C372ECF1C
ark:/67375/WNG-82990WJZ-K
Health Sector Research - No. 201002006
Ministry of Health of the People's Republic of China
ArticleID:DME12331
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ObjectType-Article-2
ObjectType-Feature-1
ISSN:0742-3071
1464-5491
1464-5491
DOI:10.1111/dme.12331