Literature DB >> 23906684

Genetic associations with coronary heart disease: meta-analyses of 12 candidate genetic variants.

Huadan Ye1, Xiaojing Li, Lingyan Wang, Qi Liao, Leiting Xu, Yi Huang, Liming Xu, Xuting Xu, Cheng Chen, Hangyu Wu, Yanping Le, Qiong Liu, Meng Ye, Changzheng Dong, Shiwei Duan.   

Abstract

AIMS: The aim of this study was to evaluate the combined contribution of 12 genetic variants to the risk of coronary heart disease (CHD).
METHODS: Through a comprehensive literature search for genetic variants involved in the CHD association study, we harvested a total of 10 genes (12 variants) for the current meta-analyses. These genes consisted of GPX1 (rs1050450), PPARD (rs2016520), ALOX15 (rs34210653), SELPLG (rs2228315), FCGR2A (rs1801274), CCL5 (rs2107538), CYP1A1 (rs4646903), TP53 (rs1042522), CX37 (rs1764391), and PECAM1 (rs668, rs12953, and rs1131012).
RESULTS: A total of 45 studies among 23,314 cases and 28,430 controls were retrieved for the meta-analyses of 12 genetic variants. The results showed a significant association between the GPX1 rs1050450 polymorphism and CHD (odd ratio (OR)=1.61, 95% confidence interval (CI)=1.25-2.07, P=0.0002). Other meta-analyses of the rest 11 variants suggested a lack of association with the risk of CHD.
CONCLUSION: Our results confirmed that GPX1 rs1050450 was associated with susceptibility to CHD in Chinese and Indian populations.
© 2013.

Entities:  

Keywords:  (12/15-LOX); (95% CI); (CHD); (CNKI); (GPx); (GWAS); (MAF); (OR); (QC); 12/15-lipoxygenases; 95% confidence interval; China National Knowledge Infrastructure; Coronary heart disease; GPX1; Genome-wide association studies; Glutathione peroxidase; Meta-analysis; Minor allele frequency; Odd ratio; Polymorphism; Quality control

Mesh:

Year:  2013        PMID: 23906684     DOI: 10.1016/j.gene.2013.07.029

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


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