PubMed:18443194 JSONTXT

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{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/18443194","sourcedb":"PubMed","sourceid":"18443194","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/18443194","text":"Differences in the contribution of the CTLA4 gene to susceptibility to fulminant and type 1A diabetes in Japanese patients.\nOBJECTIVE: To examine the contribution of the CTLA4 gene in the susceptibility to fulminant type 1 diabetes and compare it with classic type 1A diabetes.\nRESEARCH DESIGN AND METHODS: We genotyped the +49G\u003eA and CT60G\u003eA variants of the CTLA4 gene in fulminant type 1 diabetic patients (n = 55), classic type 1A diabetic patients (n = 91), and healthy control subjects (n = 369). We also assessed serum levels of the soluble form of CTLA4 (sCTLA4).\nRESULTS: The +49GG and CT60GG genotypes were associated with type 1A diabetes (P \u003c 0.001). In contrast, the CT60AA genotype, but not the +49G\u003eA variation, was associated with fulminant type 1 diabetes (P \u003c 0.05), especially in patients carrying HLA-DR4 (P \u003c 0.01). Serum levels of sCTLA4 were significantly decreased in patients with fulminant type 1 diabetes (P \u003c 0.05).\nCONCLUSIONS: These results suggest that CTLA4 CT60 affects the genetic susceptibility to fulminant type 1 diabetes. Furthermore, the contribution of CTLA4 to disease susceptibility is distinct between fulminant type 1 diabetes and classic type 1A 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