| Literature DB >> 11821159 |
Hisataka Tegoshi1, Goji Hasegawa, Hiroshi Obayashi, Koji Nakano, Yoshihiro Kitagawa, Michiaki Fukui, Satoshi Matsuo, Masako Deguchi, Mitsuhiro Ohta, Masataka Nishimura, Naoto Nakamura, Toshikazu Yoshikawa.
Abstract
We investigated the association of the polymorphisms of interferon-gamma gene (IFNG) CA-repeat and IL-10-592A/C with clinical heterogeneity of type I diabetes as well as susceptibility to type I diabetes. Two hundred seven Japanese type I diabetic patients and 160 healthy control subjects were studied in this case-control study. No significant differences of global IFNG allele frequencies were found between controls and type I diabetic patients, and between each subgroup of the patients and controls. When compared with controls, the a12 allele was increased in the patients with age at onset <25 years (p 0.0241, p(c) = 0.1205), and a significant increased frequency of the a12 positive genotype was observed in the patients with age at onset <25 years (p(c) = 0.0121). There were no differences of IL-10-592 genotype and allele frequencies between controls and type I diabetes. However, the frequency of the -592*C allele was significantly increased in the patients with highly positive-GADab compared with controls (p(c) = 0.0060) or compared with the GADab-negative type I patients (p(c) = 0.0276). These results suggest that the IFNG CA-repeat and the IL-10-592A/C polymorphisms are not strong determinants of susceptibility to the development of type I diabetes in Japanese individuals. However, both the IFNG CA-repeat and the IL-10-592A/C polymorphisms are associated with clinical heterogeneity in type I diabetes.Entities:
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Year: 2002 PMID: 11821159 DOI: 10.1016/s0198-8859(01)00363-9
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850