Associations of NKX2-5 Genetic Polymorphisms with the Risk of Congenital Heart Disease: A Meta-analysis View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2016-03-31

AUTHORS

Xiaochuan Xie, Xiaohan Shi, Xiaoshuang Xun, Li Rao

ABSTRACT

The NKX2-5 gene is a vital regulator of cardiac formation and development. Recently, the roles of NKX2-5 63A>G polymorphism and 606G>C polymorphism in congenital heart disease (CHD) have been extensively studied, with conflicting results. The aim of the present study was to better elucidate the associations between NKX2-5 genetic polymorphisms and CHD risk through a meta-analysis. Eligible articles were searched in PubMed, MEDLINE, EMBASE, Google Scholar and CNKI up to December 2015. Odds ratios (ORs) and 95 % confidence intervals were used to detect any potential associations between NKX2-5 genetic polymorphisms and CHD risk. Heterogeneity between studies was assessed with Q test and I2 statistic. Subgroup analysis and sensitivity analysis were performed to test the reliability and stability of the results, and funnel plots were applied to estimate publication bias. A total of 13 case–control studies including 2245 CHD patients and 1953 healthy controls were analyzed. The overall meta-analysis results showed that NKX2-5 63A>G polymorphism and 606G>C polymorphism were not significantly associated with CHD risk. Subgroup analysis was further performed for NKX2-5 63A>G polymorphism based on types of CHD and ethnicity of study population, and similar negative results were found in all subgroups. Our findings suggested that NKX2-5 63A>G polymorphism and 606G>C polymorphism may not be implicated in the pathogenesis of CHD. More... »

PAGES

953-961

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00246-016-1377-8

DOI

http://dx.doi.org/10.1007/s00246-016-1377-8

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1045896563

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/27033241


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