Association of polymorphisms of rs179247 and rs12101255 in thyroid stimulating hormone receptor intron 1 with an increased risk of Graves' disease: A meta-analysis.
10.1007/s11596-016-1611-x
- Author:
Jing GONG
1
;
Shu-Jun JIANG
1
;
Ding-Kun WANG
1
;
Hui DONG
1
;
Guang CHEN
1
;
Ke FANG
1
;
Jin-Rui CUI
2
;
Fu-Er LU
3
Author Information
1. Institute of Integrated Traditional Chinese and Western Medicine, Huazhong University of Science and Technology, Wuhan, 430030, China.
2. Department of Nursing Care, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
3. Institute of Integrated Traditional Chinese and Western Medicine, Huazhong University of Science and Technology, Wuhan, 430030, China. felu@tjh.tjmu.edu.cn.
- Publication Type:Journal Article
- Keywords:
Graves’ disease;
Graves’ ophthalmopathy;
genetic polymorphism;
meta-analysis
- MeSH:
China;
Female;
Genetic Association Studies;
Genetic Predisposition to Disease;
Graves Disease;
genetics;
pathology;
Graves Ophthalmopathy;
genetics;
pathology;
Humans;
Introns;
genetics;
Male;
Polymorphism, Single Nucleotide;
Receptors, Thyrotropin;
genetics;
Risk Factors
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2016;36(4):473-479
- CountryChina
- Language:English
-
Abstract:
The polymorphisms of thyroid stimulating hormone receptor (TSHR) intron 1 rs179247 and rs12101255 have been found to be associated with Graves' disease (GD) in genetic studies. In the present study, we conducted a meta-analysis to examine this association. Two reviewers systematically searched eligible studies in PubMed, Web of Science, Embase and China Biomedical Literature Database (CBM). A meta-analysis on the association between GD and TSHR intron 1 rs179247 or rs12101255 was performed. The odd ratios (OR) were estimated with 95% confidence interval (CI). Meta package in R was used for the analyses. Seven articles (13 studies) published between 2009 and 2014, involving 5754 GD patients and 5768 controls, were analyzed. The polymorphism of rs179247 was found to be associated with an increased GD risk in the allele analysis (A vs. G: OR=1.40, 95% CI=1.33-1.48) and all genetic models (AA vs. GG: OR=1.94, 95% CI=1.73-2.19; AA+AG vs. GG: OR=1.57, 95% CI=1.41-1.74; AA vs. AG+GG: OR=1.54, 95% CI=1.43-1.66). The site rs12101255 also conferred a risk of GD in the allele analysis (T vs. C: OR=1.50, 95% CI=1.40-1.60) and all genetic models (TT vs. CC: OR=2.22, 95% CI=1.92-2.57; TT+TC vs. CC: OR=1.66, 95% CI=1.50-1.83; TT vs. TC+CC: OR=1.74, 95% CI=1.53-1.98). Analysis of the relationship between rs179247 and Graves' ophthalmopathy (GO) showed no statistically significant correlation (A vs. G: OR=1.02, 95% CI=0.97-1.07). Publication bias was not significant. In conclusion, GD is associated with polymorphisms of TSHR intron 1 rs179247 and rs12101255. There is no association between rs179247 SNPs and GO.
