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Association of cytotoxic T-lymphocyte associated antigen 4 gene polymorphism with type 1 diabetes mellitus: A meta-analysis
Authors:Song-Tao Tang  Hai-Qin Tang  Qiu Zhang  Chang-Jiang Wang  You-Min Wang  Wen-Jia Peng
Institution:Department of Endocrinology, The First Affiliated Hospital of Anhui Medical University, 218 Jixi Road, Hefei230022, China.
Abstract:To evaluate the association between costimulatory molecule cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) gene polymorphism and type 1 diabetes mellitus(T1DM), sixty-three published studies before December, 2011 were included. Meta-analysis was performed for each genotype in a random/fixed effect model. The combined odds ratio (OR) with 95% confidence interval (95%CI) was calculated to estimate the strength of the association. Overall, significant correlation was noted between CTLA-4 gene polymorphism (i.e. +49A/G, CT60A/G in a per-allele model) and the risk of T1DM (for +49A/G: OR=1.47, 95%CI=1.36-1.60, P<0.001; for CT60A/G: OR=1.31, 95%CI=1.18-1.45, P<0.001). However, no significant association was noted between C(-318)T polymorphism and T1DM. In the subgroup analysis, for +49A/G and CT60A/G, the statistically significant associations were also demonstrated in diverse racial descents (Caucasian and Asian) and age of onset (<20years and >20years). In conclusion, our results suggest that CTLA-4 polymorphism contributes to the susceptibility of T1DM.
Keywords:CTLA-4  costimulatory molecule cytotoxic T-lymphocyte-associated antigen-4  T1DM  type 1 diabetes mellitus  OR  odds ratio  CI  confidence interval  PTPN22  protein tyrosine phosphatase non-receptor type 22  APC  antigen-presenting cells  HWE  Hardy–Weinberg equilibrium  PCR  polymerase chain reaction  PCR-RFLP  polymerase chain reaction with restriction fragment length polymorphism  PCR-SSCP  polymerase chain reaction with single strand conformation polymorphism  PCR-SSOP  polymerase chain reaction with sequence specific oligonucleotide probe  PCR-ARMS  polymerase chain reaction with amplification refractory mutation system  ND  no data
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