CTLA4 gene polymorphism contributes to the mode of onset of diabetes with antiglutamic acid decarboxylase antibody in Japanese patients: genetic analysis of diabetic patients with antiglutamic acid decarboxylase antibody

被引:19
作者
Abe, T
Yamaguchi, Y
Takino, H
Fujita, N
Yamauchi-Degawa, M
Ozaki, M
Yamakawa, K
Sera, Y
Sakamaki, H
Uotani, S
Kawasaki, E
Awata, T
Yamasaki, H
Eguchi, K
机构
[1] Nagasaki Univ, Sch Med, Dept Internal Med 1, Nagasaki 8528501, Japan
[2] Saitama Med Sch, Dept Internal Med 4, Moroyama, Saitama, Japan
关键词
CTLA4; GAD Ab; INS-VNTR; mode of onset;
D O I
10.1046/j.0742-3071.2001.00551.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim The mode of onset is occasionally similar in Type 1 and Type 2 diabetes mellitus, and some patients with Type 2 diabetes are positive for antiglutamic acid decarboxylase antibody (GAD Ab). We investigated the contribution of Type 1 diabetes susceptibility genes to the progression of the insulin-deficient state and mode of onset of Type 2 diabetes in GAD Ab-positive (GAD-Ab(+)) patients. We examined the variable number of tandem repeats in the promoter region of the insulin gene (INS-VNTR, insulin-dependent diabetes mellitus (IDDM) 2) and cytotoxic T lymphocyte antigen 4 (CTLA4, IDDM12) as representative of Type 1 diabetes susceptibility genes. Methods Patients with Type 2 diabetes who were GAD-Ab(+) (n = 51) were selected for this study. In INS-VNTR, the class I allele was classified according to length (1S, 25-38 repeat units; 1M, 39-41 repeat units; 1L, 42-44 repeat units) and the exact class I allele length was analysed by specific polymerase chain reaction (PCR) amplifications. Analyses of classes II and III were performed by Southern blot. CTLA4 gene polymorphism (exon 1 position 49, G/A) was analysed by PCR-restriction fragment length polymorphism. Results The distribution of INS-VNTR was no different between Type 1 diabetes and Type 2 diabetes with GAD Ab. The allele frequencies of CTLA4 gene polymorphism G and A in Type 2 diabetes/GAD-Ab(+) were significantly different from those of Type 1 diabetes/GAD-Ab(+) (G: 53%, A: 47% vs. G: 84%, A: 16%; P < 0.0001). Conclusions Our data showed that GAD-Ab(+) Japanese patients presenting with Type 2 diabetes have shifted A allele while patients with abrupt onset have shifted G allele of CTLA4 gene polymorphism. Our results suggest that immunological function and polymorphism of the CTLA4 gene may contribute to the pathogenesis and progression of Type 1 diabetes.
引用
收藏
页码:726 / 731
页数:6
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