Oncotarget

Meta-Analysis:

Association between rs3087243 and rs231775 polymorphism within the cytotoxic T-lymphocyte antigen 4 gene and Graves’ disease: a case/control study combined with meta-analyses

Yaqin Tu, Guorun Fan, Yu Dai, Tianshu Zeng, Fei Xiao, Lulu Chen and Wen Kong _

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Oncotarget. 2017; 8:110614-110624. https://doi.org/10.18632/oncotarget.22702

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Abstract

Yaqin Tu1,*, Guorun Fan1,*, Yu Dai3, Tianshu Zeng2, Fei Xiao2, Lulu Chen2 and Wen Kong2

1Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China

2Department of Endocrinology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China

3Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China

*These authors contributed equally to this work

Correspondence to:

Wen Kong, email: wenly-kong@163.com

Lulu Chen, email: cheria_chen@126.com

Keywords: Graves’ disease; cytotoxic T-lymphocyte antigen 4; polymorphism; susceptibility; case/control study

Received: April 21, 2017     Accepted: October 30, 2017     Published: November 27, 2017

ABSTRACT

We conducted a case/control study to assess the impact of SNP rs3087243 and rs231775 within the CTLA4 gene, on the susceptibility to Graves’ disease (GD) in a Chinese Han dataset (271 cases and 298 controls). The frequency of G allele for rs3087243 and rs231775 was observed to be significantly higher in subjects with GD than in control subjects (p = 0.005 and p = 0.000, respectively). After logistic regression analysis, a significant association was detected between SNP rs3087243 and GD in the additive and recessive models. Similarly, association for the SNP rs231775 could also be detected in the additive model, dominant model and recessive model. A meta-analysis, including 27 published datasets along with the current dataset, was performed to further confirm the association. Consistent with our case/control results, rs3087243 and rs231775 showed a significant association with GD in all genetic models. Of note, ethnic stratification revealed that these two SNPs were associated with susceptibility to GD in populations of both Asian and European descent. In conclusion, our data support that the rs3087243 and rs231775 polymorphisms within the CTLA4 gene confer genetic susceptibility to GD.


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