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Article type: Research Article
Authors: Meguid, Nagwa A. | Dardir, Ahmed A. | Khass, Mohamed | Hossieny, Lamia El | Ezzat, Afaf | Awady, Mostafa K. El
Affiliations: Department of Research on Children with Special Needs, National Research Center, Cairo, Egypt | Department of Biomedical Technology, National Research Center, Cairo, Egypt | Department of Nutrition and Food Science, National Research Center, Cairo, Egypt
Note: [] Corresponding author: Prof. Nagwa A. Meguid, Prof. of Human Genetics & Head of Department of Research on Children with Special Needs, National Research Center, Tahrir St., Cairo, Egypt. Tel.: +20 12 331 6372; Fax: +20 2 337 0931, +20 2 760 1877; E-mail: [email protected]
Abstract: Recent reports linking Down syndrome (DS) to maternal polymorphisms at the methylenetetrahydrofolate reductase (MTHFR) gene locus have generated great interest among investigators in the field. The present study aimed at evaluation of MTHFR 677C/T and 1298A/C polymorphisms in the MTHFR gene as maternal risk factors for DS. Forty two mothers of proven DS outcomes and forty eight control mothers with normal offspring were included. Complete medical and nutritional histories for all mothers were taken with special emphasis on folate intake. Folic acid intake from food or vitamin supplements was significantly low (below the Recommended Daily Allowance) in the group of case mothers compared to control mothers. Frequencies of MTHFR 677T and MTHFR 1298C alleles were significantly higher among case mothers (32.1% and 57.1%, respectively) compared to control mothers (18.7% and 32.3%, respectively). Heterozygous and homozygous genotype frequencies of MTHFR at position 677 (CT and TT) were higher among case mothers than controls (40.5% versus 25% and 11.9% versus 6.2%, respectively) with an odds ratio of 2.34 (95% confidence interval [CI] 0.93–5.89) and 2.75 (95% CI 0.95–12.77), respectively. Interestingly, the homozygous genotype frequency (CC) at position 1298 was significantly higher in case mothers than in controls (33.3% versus 2.1% respectively) with an odds ratio of 31.5 (95% CI 3.51 to 282.33) indicating that this polymorphism may have more genetic impact than 677 polymorphism. Heterozygous genotype (AC) did not show significant difference between the two groups. We here report on the first pilot study of the possible genetic association between DS and MTHFR 1298A/C genotypes among Egyptians. Further extended studies are recommended to confirm the present work.
Keywords: Methylenetetrahydrofolate reductase (MTHFR), Down syndrome, polymorphism, MTHFR 677C/T polymorphism, MTHFR 1298A/C polymorphism, Egyptian
Journal: Disease Markers, vol. 24, no. 1, pp. 19-26, 2008
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