Association between PKA gene polymorphism and NTDs in high risk Chinese population in Shanxi.
Int J Clin Exp Pathol
; 6(12): 2968-74, 2013.
Article
em En
| MEDLINE
| ID: mdl-24294386
ABSTRACT
OBJECTIVE:
This study aimed to investigate the single nucleotide polymorphisms (SNPs) of PKA and neural tube defects (NTDs) in Chinese population.METHOD:
A total of 183 NTDs cases and 200 healthy controls were used in this study. 7 selected single nucleotide polymorphism (SNP) sites in the PKA gene were analyzed with MassArray high-throughput DNA analyzer with matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. A series of statistical methods were carried out to investigate the correlation between the SNPs and the patient susceptibility to NTDs.RESULTS:
Statistical analysis showed a significant correlation between the SNP sites rs12132032 in PRKACB and NTDs. The AA genotype, A-allele and dominant AA in rs12132032 significantly increased the incidence of NTDs especially anencephaly (OR=3.87, 95% CI 1.80-8.34 with genotype; OR=2.08, 95% CI 1.43-3.04 with allele; OR=3.10, 95% CI 1.53-6.26 with dominant). The T-allele of rs594631 in PRKACB was correlative with NTDs in male but not in female.CONCLUSIONS:
The gene polymorphism loci rs12132032 in PRKACB maybe a potential risk factor for anencephaly in Chinese population from Shanxi, while gender susceptibility may influence the correlation.Palavras-chave
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Base de dados:
MEDLINE
Assunto principal:
Povo Asiático
/
Subunidades Catalíticas da Proteína Quinase Dependente de AMP Cíclico
/
Defeitos do Tubo Neural
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article