Tian Jinfeng, Wei Yuan, Wang Liang, Guo Jinzhen, Zhou Qian, Zhu Wenli
Wei Sheng Yan Jiu. 2015 Jul;44(4):543-8.
To explore the relationship between polymorphism of interferon regulatory factor 6 (IRF6) gene rs642961 locus and nonsyndromic cleft lip with or without cleft palate (NSCL ± P).
There were 88 NSCL ± P nuclear families and 116 healthy people as control recruited from Chinese northern area. The polymorphism of IRF6 rs642961 locus was detected by tetra-primer amplification refractory mutation system-polymerase chain reaction (tetra-primer ARMS-PCR). Case-control analysis, transmission-disequilibrium test (TDT), haplotype-based haplotype relative risk analysis (HHRR) and family-based association test (FBAT) were carried out.
There was significant difference in rs642961 of IRF6 locus between the NSCL P group and control group, whether in children or parents (P < 0.05). The odds ratio (OR) of AG and AA versus GG is above one, and its 95% confidence interval did not include 1 in offspring, father and mother group, which meant genetic variant of rs642961 of IRF6 could increase the risk of occurrence of NSCL ± P. The allele transmission disequilibrium for rs642961 of IRF6 variant in NSCL ± P families was found by TDT analysis (P < 0.05). HHRR calculation also showed that there was association between the genetic variant and the occurrence of NSCL ± P (P < 0.05). While FBAT test showed that there was relationship between the genetic variant and the occurrence of NSCL ± P in addictive model.
Polymorphism IRF6 gene locus is associated with NSCL ± P in northern Chinese population.
探讨干扰素调节因子6(IRF6)基因rs642961位点多态性与非综合征性唇裂伴或不伴腭裂(NSCL±P)之间的关系。
从中国北方地区招募88个NSCL±P核心家庭和116名健康人作为对照。采用四引物扩增阻滞突变系统-聚合酶链反应(四引物ARMS-PCR)检测IRF6 rs642961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)。
NSCL±P组与对照组在IRF6基因座的rs642961位点上存在显著差异,无论是儿童还是父母(P<0.05)。在子代、父亲和母亲组中,AG和AA相对于GG的优势比(OR)均大于1,其95%置信区间不包括1,这意味着IRF6基因rs642961位点的基因变异可增加NSCL±P的发病风险。通过TDT分析发现NSCL±P家庭中IRF6基因变异体rs642961的等位基因传递不平衡(P<0.05)。HHRR计算也显示该基因变异与NSCL±P的发生有关(P<0.05)。而FBAT检验表明在成瘾模型中该基因变异与NSCL±P的发生有关。
在中国北方人群中,IRF6基因座多态性与NSCL±P有关。