CTLA-4+49A/G gene polymorphism and type 1 diabetes mellitus in the Chinese population: a meta-analysis of 2238 subjects

被引:2
作者
Li, Yan-yan [1 ]
Gong, Ge [1 ]
Geng, Hong-yu [1 ]
Yang, Zhi-jian [1 ,2 ]
Zhou, Chuan-wei [1 ]
Lu, Xin-zheng [2 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Geriatr, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Dept Cardiol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Cytotoxic T lymphocyte-associated antigen 4; +49A/G; Polymorphism; Type 1 diabetes mellitus; A/G POLYMORPHISM; AUTOIMMUNE-DISEASE; CTLA4; LOCUS; ASSOCIATION; SUSCEPTIBILITY; VARIANT; CHILDREN; IDDM; ALLELES; BIAS;
D O I
10.1007/s13410-015-0414-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Previous studies reported that cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) +49A/G gene polymorphism is correlated with type 1 diabetes mellitus (T1DM) risk. However, their results remain disputable. This study aims to discuss the relationship between CTLA-4 +49A/G gene polymorphism and T1DM in a Chinese population. The current meta-analysis involved 2238 participants from seven individual studies. The pooled odds ratio (OR) and its corresponding 95 % confidence interval (95 % CI) were assessed by the random- or fixed-effects model. A significant relationship between CTLA-4 +49A/G gene polymorphism and T1DM was detected under allelic (OR: 1.84, 95 % CI: 1.62-2.10, P < 0.00001), dominant (OR: 1.152, 95 % CI: 1.062-1.249, P = 0.001), recessive (OR: 1.631, 95 % CI: 1.443-1.844, P < 0.00001), and additive (OR: 1.292, 95 % CI: 1.224-1.363, P < 0.00001) genetic models. A significant relationship exists between CTLA-4 +49A/G gene polymorphism and increased T1DM risk in the Chinese population. Individuals having the G allele of CTLA-4 +49A/G gene polymorphism have a higher risk for T1DM in the Chinese population.
引用
收藏
页码:45 / 51
页数:7
相关论文
共 36 条
[31]  
Vijayakrishnan L, 2004, IMMUNITY, V20, P563, DOI 10.1016/S1074-7613(04)00110-4
[32]  
Wang L., 2001, CHINESE J ENDOCRINOL, V17, P228
[33]   Changes in frequency of IDDM-associated HLA DQB, CTLA4 and INS alleles [J].
Witas, H. W. ;
Jedrychowska-Danska, K. ;
Zawicki, P. .
INTERNATIONAL JOURNAL OF IMMUNOGENETICS, 2010, 37 (03) :155-158
[34]  
Xiang B., 2006, J CLIN RES, V23, P1521
[35]  
Yang J.J., 2006, J NINGXIA MED COLL, V28, P374
[36]  
Zhang SW, 2005, CHIN MED J, V85, P788