The relationship between frizzled 6 gene polymorphisms and neural tube defects in children of northern Han Chinese population

Q4 Medicine
Chunquan Cai, O. Shi, Yongxiang Shen, Xiao Ma
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Abstract

Objective To study the association of single nucleotide polymorphisms (SNPs) of the frizzled 6 (FZD6) gene with neural tube defects (NTDs) in a northern Han Chinese population. Methods Three nonsynonymous SNPs in the FZD6 gene (rs827528,rs3808553,rs12549394) were examined.The SNPs were genotyped by polymerase chain reaction (PCR) and sequencing in 135 NTD patients and matched normal controls.The allele,genotype and haplotype frequencies were calculated and analyzed to examine the association between FZD6 SNPs and NTDs. Results Both T allele and TT genotype frequencies of the rs3808553 polymorphism in the NTDs group were significantly higher than those in the controls,and children with T allele and TT genotype were associated with increased risk of NTDs (OR=1.575,95% CI 1.112-2.230,P=0.010 and OR=2.811,95% CI 1.325-5.967,P=0.023 respectively).There were no significant differences among different genotypes or alleles in both rs827528 and rs12549394.Haplotypes A-G-C and A-T-C were found associated with NTDs in the case-control study (OR=0.560,95% CI 0.378-0.830,P=0.004 and OR=1.670,95% CI 1.126-2.475,P=0.011 respectively). Conclusions The rs3808553 polymorphism of FZD6 s obviously associated with NTDs in children of northern Han Chinese population.The TT genotype may increase the risk for NTDs.The rs827528 and rs12549394 polymorphisms of FZD6 may have no association with NTDs. Key words: Neural tube defects; Frizzled receptors; Polymorphisms,single nucleotide
北方汉族儿童卷曲6基因多态性与神经管缺陷的关系
目的研究北方汉族人群卷曲6 (FZD6)基因单核苷酸多态性与神经管缺陷(NTDs)的关系。方法检测FZD6基因的3个非同义snp (rs827528、rs3808553、rs12549394)。通过聚合酶链反应(PCR)和测序对135例NTD患者和匹配的正常对照进行基因分型。计算并分析等位基因、基因型和单倍型频率,以检验FZD6 snp与NTDs的相关性。结果NTDs组rs3808553多态性的T等位基因和TT基因型频率均显著高于对照组,携带T等位基因和TT基因型的患儿患NTDs的风险增加(OR=1.575,95% CI 1.112 ~ 2.230,P=0.010; OR=2.811,95% CI 1.325 ~ 5.967,P=0.023)。rs827528和rs12549394在不同基因型和等位基因间无显著差异。病例对照研究发现单倍型A-G-C和A-T-C与NTDs相关(OR=0.560,95% CI 0.378 ~ 0.830,P=0.004; OR=1.670,95% CI 1.126 ~ 2.475,P=0.011)。结论北方汉族儿童FZD6基因rs3808553多态性与NTDs有明显相关性。TT基因型可能增加被忽视热带病的风险。FZD6的rs827528和rs12549394多态性可能与NTDs无关。关键词:神经管缺损;卷曲的受体;多态性,单核苷酸
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来源期刊
中华神经科杂志
中华神经科杂志 Medicine-Neurology (clinical)
CiteScore
0.70
自引率
0.00%
发文量
6868
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