Murthy Jyotsna, Lakkakula Saikrishna, Gurramkonda Venkatesh Babu, Pathapati Ram Mohan, Maram Rajasekhar, Lakkakula Bhaskar V K S
Cleft Palate Craniofac J. 2015 Jan;52(1):49-53. doi: 10.1597/13-051.
Nonsyndromic cleft lip with or without cleft palate (NSCLP) is a common birth defect with substantial clinical and social impact. Folate deficiency is one of the factors that have been associated with increased risk for NSCLP. Polymorphisms in folate and homocysteine pathway genes may act as susceptibility factors.
The objective of this study was to evaluate prevalence estimates of cystathionine beta-synthase (CBS) insertion of 68-bp (c.844ins68) polymorphisms and their correlation with NSCLP.
A total of 236 unrelated individuals from seven Indian populations and an additional 355 cases with NSCLP and 357 controls without NSCLP were included in this study. We investigated the CBS c.844ins68 polymorphism in all samples. Genotyping was performed with polymerase chain reaction and electrophoresis. The data were statistically analyzed using the chi-square test.
The CBS c.844ins68 allele is present in six of the seven populations analyzed, and allele frequencies range from 1.5% in Balija to 9.1% in Sugali populations. The CBS c.844ins68 polymorphism showed a significant protective effect on NSCLP at both genotype (WW versus WI: odds ratio [OR] = 0.54, 95% confidence interval [CI] = 0.31 to 0.95, P = .149) and allele levels (W versus I: OR = 0.56, 95% CI = 0.32 to 0.96, P = .033).
The current study observed significant differences in the frequency of the CBS 844ins68 allele across populations. There is a significant association between CBS c.844ins68 polymorphism and cleft lip and palate in the Indian population. Additional studies are warranted to identify the functional variants in the genes controlling homocysteine as etiological contributors to the formation of oral clefts.
非综合征性唇裂伴或不伴腭裂(NSCLP)是一种常见的出生缺陷,具有重大的临床和社会影响。叶酸缺乏是与NSCLP风险增加相关的因素之一。叶酸和同型半胱氨酸途径基因的多态性可能是易感因素。
本研究的目的是评估胱硫醚β-合酶(CBS)68-bp插入(c.844ins68)多态性的患病率估计及其与NSCLP的相关性。
本研究共纳入来自七个印度人群的236名无关个体,以及另外355例NSCLP患者和357例无NSCLP的对照。我们在所有样本中研究了CBS c.844ins68多态性。采用聚合酶链反应和电泳进行基因分型。使用卡方检验对数据进行统计学分析。
在分析的七个群体中的六个群体中存在CBS c.844ins68等位基因,等位基因频率范围从Balija群体中的1.5%到Sugali群体中的9.1%。CBS c.844ins68多态性在基因型(WW与WI:比值比[OR]=0.54,95%置信区间[CI]=0.31至0.95,P=.149)和等位基因水平(W与I:OR=0.56,95%CI=0.32至0.96,P=.033)上均对NSCLP显示出显著的保护作用。
本研究观察到CBS 844ins68等位基因频率在不同群体之间存在显著差异。在印度人群中,CBS c.844ins68多态性与唇腭裂之间存在显著关联。有必要进行更多研究以确定控制同型半胱氨酸的基因中的功能变异,作为口腔裂隙形成的病因学因素。