Methionine synthase A2756G and reduced folate carrier1 A80G gene polymorphisms as maternal risk factors for Down syndrome in Egypt

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• 作者：Maha Moustafa^a ; ^{mmkmahmed@yahoo.com" class="auth_mail" title="E-mail the corresponding author} ; Elham Gaber^b ; Gamal Abo El Fath^c
• 关键词：DS ; Down syndrome ; MTR ; methionine synthase ; RFC ; reduced folate carrier
• 刊名：Egyptian Journal of Medical Human Genetics
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：17
• 期：2
• 页码：217-221
• 全文大小：424 K

文摘

Polymorphisms of genes encoding enzymes involved in folate metabolism have long been hypothesized to be maternal risk factors for Down syndrome, however, results are conflicting and inconclusive.

Aim of the study

To analyze the effect of methionine synthase (MTR) A2756G, and reduced folate carrier (RFC1) A80G gene polymorphisms on the maternal risk for DS.

Patients

This study was conducted in the Medical Genetics Center, Ain-Shams University hospitals, on a total of 170 mothers of children, diagnosed with Down syndrome, who were attending the center. Eighty-five control mothers were also enrolled in the study.

Methods

Genotype analyses were performed using PCR-RFLP to detect RFC1A80G and MTRA2756G gene polymorphisms in all case and control mothers.

Results

Comparing RFC1A80G genotype frequency between both groups revealed, that the frequency of the AA genotype in case mothers (94.11%) is highly significantly (p < 0.001) greater than its frequency in control mothers (74.11%), with no significant difference between the two groups regarding GG genotype. Comparing RFC1 A80G allele frequency between the two groups revealed a high frequency of the A allele among case mothers (94.11%), which showed a highly statistically significant difference (p < 0.001) from the control group (55.29%), meanwhile the G allele showed a low frequency of 5.88% in DS mothers compared to 22.35% in the control mothers, with a highly statistically significant difference (p < 0.001) between the two groups. Regarding MTRA2756G polymorphism, it was found that the AA genotype predominated in the control group (65.88%) with a highly statistically significant difference (p < 0.001) from case mothers group (5.88%). Comparing MTR allele frequency between the two groups revealed predominance of the G allele among mothers of DS children (76.47%).

Conclusion

Current results provide strong evidence that the MTRA2756G, and RFC1 80 A genotypes could be considered as maternal risk factors for DS in Egyptian mothers.