Literature DB >> 26770549

Correlation between rs198388 and rs198389 polymorphismsin brainnatriuretic peptide (NPPB) gene and susceptibility to congenital heart diseases in a Chinese population.

Qing Zhang1, Fang-Qi Gong1, Wei-Hua Zhu1, Chun-Hong Xie1, Yi-Ying Zhang1, Li-Yang Ying1.   

Abstract

OBJECTIVE: We discussed the correlation between SNP loci (rs198389 and rs198388) in brain natriuretic peptide gene (NPPB) and susceptibility to congenital heart diseases (CHD).
METHOD: Multiplex SNaPshot technique was adopted for profiling of SNP genotypes at loci rs198389 and rs198388 in NPPB gene among 150 cases of CHDand 150 normal controls.
RESULTS: The distribution frequency of 3 genotypes (AA, AG and GG) at locus rs198389 was 40.7%, 36.0% and 23.3% in CHD group, respectively, showing significant differences compared with the normal controls (P<0.001). Gallele was associated with higher risk of CHD (OR=2.48, 95% CI=1.77-3.48). The distribution frequency of CC, CTand TT genotypes at locus rs198388 was 60.7%, 17.3% and 22.0% in CHD group, respectively, also showing significant differences compared with the normal controls (P<0.001). C allele could increase the risk of CHD (OR=1.92, 95% CI=1.48-2.48).
CONCLUSION: SNP loci rs198389 and rs198388 in NPPB gene were correlated with genetic susceptibility to CHD.

Entities:  

Keywords:  Brain natriuretic peptide (NPPB); congenital heart disease (CHD); genetic susceptibility; single nucleotide polymorphism (SNP)

Year:  2015        PMID: 26770549      PMCID: PMC4694449     

Source DB:  PubMed          Journal:  Int J Clin Exp Med        ISSN: 1940-5901


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