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5,10-亚甲基四氢叶酸还原酶和胱硫醚β-合酶基因多态性作为阿尔及利亚塞蒂夫神经管缺陷的危险因素

Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria.

作者信息

Houcher Bakhouche, Bourouba Romyla, Djabi Farida, Yilmaz Erkan, Eğin Yonca, Akar Nejat

机构信息

Department of Biology, Faculty of Sciences, University of Sétif, 19000 Sétif, Algeria.

出版信息

Pediatr Neurosurg. 2009;45(6):472-7. doi: 10.1159/000283086. Epub 2010 Feb 16.

Abstract

BACKGROUND

Neural tube defects (NTD) are severe congenital malformations due to a failure in neural tube formation at the beginning of pregnancy. The etiology of NTD is multifactorial, with environmental and genetic determinants. We suggest a study of gene-gene interactions regarding the possible association of NTD with specific mutations of 5,10-methylenetetrahydrofolate reductase (MTHFR) and cystathionine beta-synthase (CBS) genes.

PATIENTS AND METHODS

The genetic analysis of the MTHFR C677T polymorphism was performed by real-time polymerase chain reaction (PCR) on a Light Cycler, the CBS genotype was analyzed by PCR in a thermal cycler. Ninety-two mothers who had conceived NTD children and 48 fathers were investigated. A group of 147 adults, including 82 apparently healthy women, was used as control.

RESULTS

Among control mothers, 35 (43%) were heterozygous for the C677T variant and 14 (17%) were TT homozygous. Among the cases, 25 (52%) out of 48 mothers and 22 (46%) out of 48 fathers carried the T allele; 9 mothers (19%) and 5 fathers (10%) had the TT genotype. A homozygous C677T mutation was not an NTD risk factor in this preliminary study in an Algerian population; a possible gene-gene interaction between the MTHFR C677T polymorphism and the CBS 844ins68 has also been examined in relation to NTD, but no such association has been shown. There was a statistically significant difference between the heterozygosity genotype frequency of CBS polymorphisms in mothers with a previous child with NTD compared with the mother controls (odds ratio: 3.72; 95% CI: 1.59-8.73).

CONCLUSION

Our results with Algerian NTD mothers did not show a significant association for any group, suggesting that the thermolabile variant C677T in the MTHFR gene is not a risk factor for a mother to have NTD offspring; rather, folic acid supplementation or fortification should become mandatory for all women of reproductive age in Algeria.

摘要

背景

神经管缺陷(NTD)是由于妊娠初期神经管形成失败导致的严重先天性畸形。NTD的病因是多因素的,包括环境和遗传因素。我们建议研究基因-基因相互作用,探讨NTD与5,10-亚甲基四氢叶酸还原酶(MTHFR)和胱硫醚β-合酶(CBS)基因特定突变之间的可能关联。

患者与方法

采用实时聚合酶链反应(PCR)在Light Cycler上对MTHFR C677T多态性进行基因分析,在热循环仪上通过PCR分析CBS基因型。对92名生育神经管缺陷患儿的母亲和48名父亲进行了调查。选取147名成年人组成对照组,其中包括82名明显健康的女性。

结果

在对照母亲中,35名(43%)为C677T变异的杂合子,14名(17%)为TT纯合子。在病例组中,48名母亲中有25名(52%)、48名父亲中有22名(46%)携带T等位基因;9名母亲(19%)和5名父亲(10%)具有TT基因型。在阿尔及利亚人群的这项初步研究中,纯合C677T突变不是NTD的危险因素;还研究了MTHFR C677T多态性与CBS 844ins68之间与NTD相关的可能基因-基因相互作用,但未发现此类关联。与母亲对照组相比,曾生育神经管缺陷患儿的母亲中CBS多态性杂合子基因型频率存在统计学显著差异(优势比:3.72;95%置信区间:1.59-8.73)。

结论

我们对阿尔及利亚神经管缺陷母亲的研究结果未显示任何组之间存在显著关联,这表明MTHFR基因中热不稳定变异C677T不是母亲生育神经管缺陷后代的危险因素;相反,阿尔及利亚所有育龄妇女都应强制补充或强化叶酸。

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