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[IRF6基因rs2235371位点多态性与非综合征性唇裂伴或不伴腭裂的关联]

[Association between polymorphism of IRF6 rs2235371 locus and nonsyndromic cleft lip with or without cleft palate].

作者信息

Li Meng-jie, Zhu Wen-li, Wang Yun, Guo Jin-zhen, Li Shu-qin, Li Yong

机构信息

Department of Nutrition and Food Hygiene, Peking University, Beijing, People's Republic of China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Apr;29(2):149-54. doi: 10.3760/cma.j.issn.1003-9406.2012.02.007.

Abstract

OBJECTIVE

To assess the association between polymorphism of interferon regulatory factor 6 (IRF6) gene rs2235371 locus and nonsyndromic cleft lip with or without cleft palate in Chinese population.

METHODS

Blood samples from 106 patients and their parents and 129 controls and their parents were collected. The polymorphism of IRF6 rs2235371 locus was determined with PCR-restriction fragment length polymorphism (PCR-RFLP) method. Case-control analysis, transmission disequilibrium test(TDT), haplotype-based haplotype relative risk analysis (HHRR) and family-based association test (FBAT) were carried out.

RESULTS

By case-control analysis, no significant difference was found in the frequencies of GG, GA and AA genotypes of rs2235371 locus between the patient group and control group (P> 0.05), but there was a significant difference in allelic frequencies (P< 0.05). There was also a significant difference in genotype and gene frequencies of rs2235371 variant between family members from cleft lip only group and control group. However, in cleft lip with cleft palate group, no such difference was observed. TDT analysis suggested a linkage in the presence of disequilibrium (chi-square=5.56, P=0.024). Results of HHRR analysis (chi-square=5.115, P=0.024) and FBAT (Z=2.218, P=0.027) also indicated an association between IRF6 rs2235371 variant and the risk of NSCL with or without cleft palate.

CONCLUSION

Genetic polymorphism of IRF6 gene rs2235371 locus is associated with NSCL with or without cleft palate.

摘要

目的

评估中国人群中干扰素调节因子6(IRF6)基因rs2235371位点多态性与非综合征性唇裂伴或不伴腭裂之间的关联。

方法

收集106例患者及其父母以及129例对照及其父母的血样。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法检测IRF6 rs2235371位点的多态性。进行病例对照分析、传递不平衡检验(TDT)、基于单倍型的单倍型相对风险分析(HHRR)和基于家系的关联检验(FBAT)。

结果

病例对照分析显示,rs2235371位点的GG、GA和AA基因型频率在患者组和对照组之间无显著差异(P>0.05),但等位基因频率有显著差异(P<0.05)。仅唇裂组家庭成员与对照组之间rs2235371变异的基因型和基因频率也有显著差异。然而,在唇裂伴腭裂组中未观察到这种差异。TDT分析表明存在不平衡时的连锁关系(卡方=5.56,P=0.024)。HHRR分析(卡方=5.115,P=0.024)和FBAT(Z=2.218,P=0.027)的结果也表明IRF6 rs2235371变异与非综合征性唇裂伴或不伴腭裂的风险相关。

结论

IRF6基因rs2235371位点的基因多态性与非综合征性唇裂伴或不伴腭裂相关。

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