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Genet Test Mol Biomarkers ; 28(6): 263-266, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38717090

ABSTRACT

Background: Several studies in mothers of infants with Down syndrome (DS) (MoIDS) have suggested that the 677C>T and 1298A>C variants of the 5,10-methylentetrahydrofolate reductase (MTHFR) gene can increase the risk of having a child with DS. Aim: This study aimed to evaluate the MTHFR 677C>T and 1298A>C variants as potential maternal risk factors for DS. Materials and Methods: Using TaqMan allelic discrimination assay, we genotyped 95 MoIDS and 164 control mothers from western Mexico. Data were analyzed using logistic regression analysis. Results: We found that MoIDS had a significantly higher risk for the MTHFR 677TT genotype (adjusted odds ratio [aOR] = 3.4, 95% confidence interval [95% CI]: 1.1-10.6), and the MTHFR 677T allele (aOR = 1.5, 95% CI: 1.0-2.3), particularly in MoIDS <35 years of age. Conclusions: Our findings indicate that the presence of the 677TT genotype and 677T allele of the MTHFR 677C>T variant are maternal risk factors for DS in Mexican MoIDS.


Subject(s)
Alleles , Down Syndrome , Genetic Predisposition to Disease , Genotype , Methylenetetrahydrofolate Reductase (NADPH2) , Mothers , Polymorphism, Single Nucleotide , Humans , Down Syndrome/genetics , Methylenetetrahydrofolate Reductase (NADPH2)/genetics , Mexico/epidemiology , Female , Adult , Infant , Polymorphism, Single Nucleotide/genetics , Risk Factors , Genetic Predisposition to Disease/genetics , Case-Control Studies , Gene Frequency/genetics , Male , Pregnancy , Odds Ratio , Infant, Newborn
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