Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria
- PMID: 20160465
- DOI: 10.1159/000283086
Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria
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.
Copyright 2010 S. Karger AG, Basel.
Comment in
-
Polymorphisms of 5,10-Methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria. Concerning the article by Houcher et al., Pediatr Neurosurg 2009;45:472-477.Pediatr Neurosurg. 2009;45(6):478. doi: 10.1159/000283087. Epub 2010 Feb 16. Pediatr Neurosurg. 2009. PMID: 20164651 No abstract available.
Similar articles
-
Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population.J Hum Genet. 2001;46(3):105-9. doi: 10.1007/s100380170096. J Hum Genet. 2001. PMID: 11310576
-
Polymorphisms of 5,10-Methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria. Concerning the article by Houcher et al., Pediatr Neurosurg 2009;45:472-477.Pediatr Neurosurg. 2009;45(6):478. doi: 10.1159/000283087. Epub 2010 Feb 16. Pediatr Neurosurg. 2009. PMID: 20164651 No abstract available.
-
Impact of 5,10-methylenetetrahydrofolate reductase gene polymorphism on neural tube defects.J Neurosurg Pediatr. 2010 Oct;6(4):364-7. doi: 10.3171/2010.8.PEDS1072. J Neurosurg Pediatr. 2010. PMID: 20887110
-
Genetic basis of neural tube defects. II. Genes correlated with folate and methionine metabolism.J Appl Genet. 2002;43(4):511-24. J Appl Genet. 2002. PMID: 12441636 Review.
-
"Polymorphisms in folate metabolism genes as maternal risk factor for neural tube defects: an updated meta-analysis".Metab Brain Dis. 2015 Feb;30(1):7-24. doi: 10.1007/s11011-014-9575-7. Epub 2014 Jul 9. Metab Brain Dis. 2015. PMID: 25005003 Review.
Cited by
-
Finding the genetic mechanisms of folate deficiency and neural tube defects-Leaving no stone unturned.Am J Med Genet A. 2017 Nov;173(11):3042-3057. doi: 10.1002/ajmg.a.38478. Epub 2017 Sep 25. Am J Med Genet A. 2017. PMID: 28944587 Free PMC article. Review.
-
Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies.PLoS One. 2012;7(10):e41689. doi: 10.1371/journal.pone.0041689. Epub 2012 Oct 3. PLoS One. 2012. PMID: 23056169 Free PMC article.
-
Genetic studies of the cystathionine beta-synthase gene and myelomeningocele.Birth Defects Res A Clin Mol Teratol. 2012 Jan;94(1):52-6. doi: 10.1002/bdra.22855. Epub 2011 Sep 28. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 21957013 Free PMC article.
-
Association of SMO polymorphisms and neural tube defects in the Chinese population from Shanxi Province.Int J Clin Exp Med. 2013 Oct 25;6(10):960-6. eCollection 2013. Int J Clin Exp Med. 2013. PMID: 24260604 Free PMC article.
-
Association between MTHFD1 G1958A polymorphism and neural tube defects susceptibility: a meta-analysis.PLoS One. 2014 Jun 30;9(6):e101169. doi: 10.1371/journal.pone.0101169. eCollection 2014. PLoS One. 2014. PMID: 24977710 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical