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Prevalence of methylenetetrahydrofolate reductase gene polymorphisms (C677T, and A1298C) among Saudi children receiving dental treatment
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BACKGROUND:
Methylenetetrahydrofolate reductase, the encoded by the
MTHFR
gene, plays a crucial role in converting the amino acid homocysteine to methionine. Two polymorphisms of the
MTHFR
gene, C677T and A1298C, reportedly reduce enzyme activity, resulting in hyperhomocysteinemia. Patients with C677T and A1298C polymorphisms may be at higher risk for developing abnormal hyperhomocysteinemia, which has been linked to catastrophic neurological including fatal outcomes.
OBJECTIVE:
Determine the prevalence of the
MTHFR
gene variants C677T and A1298C among pediatric dental patients treated at King Abdulaziz University Hospital.
DESIGN:
Cross-sectional.
SETTING:
Clinics of pediatric dentistry department.
SUBJECTS AND METHODS:
Healthy Saudi children 6–12 years old with no known allergies were screened for eligibility between May and December 2019. A single investigator collected saliva samples. The
MTHFR
C677T and A1298C polymorphisms were analyzed using polymerase chain reaction and restriction fragment length polymorphism.
MAIN OUTCOME MEASURE:
The prevalence of
MTHFR
gene variants (C677T and A1298C) among the subjects.
SAMPLE SIZE:
138.
RESULTS:
MTHFR
C677T polymorphism was present in 36.2% of the sample and 90.0% of children carrying this allele were heterozygotes.
MTHFR
A1298C polymorphism was present in 91.3% of the sample and 77.0% of the children carrying this allele were heterozygotes. No linkage disequilibrium between
MTHFR
C677T and
MTHFR
A1298C was observed within this sample.
CONCLUSIONS:
Our study found a high frequency of the
MTHFR
A1298C genotype, which was substantially more abundant than expected based on a Hardy-Weinberg distribution. Therefore, caution is advised in using N
2
O in Saudi children as the increased prevalence of this
MTHFR
allele may increase the incidence of serious adverse effects among these children.
LIMITATIONS:
Further studies are recommended with a larger sample size from randomly selected hospitals from different regions of Saudi Arabia.
CONFLICT OF INTEREST:
None.
King Faisal Specialist Hospital and Research Centre
Title: Prevalence of methylenetetrahydrofolate reductase gene polymorphisms (C677T, and A1298C) among Saudi children receiving dental treatment
Description:
BACKGROUND:
Methylenetetrahydrofolate reductase, the encoded by the
MTHFR
gene, plays a crucial role in converting the amino acid homocysteine to methionine.
Two polymorphisms of the
MTHFR
gene, C677T and A1298C, reportedly reduce enzyme activity, resulting in hyperhomocysteinemia.
Patients with C677T and A1298C polymorphisms may be at higher risk for developing abnormal hyperhomocysteinemia, which has been linked to catastrophic neurological including fatal outcomes.
OBJECTIVE:
Determine the prevalence of the
MTHFR
gene variants C677T and A1298C among pediatric dental patients treated at King Abdulaziz University Hospital.
DESIGN:
Cross-sectional.
SETTING:
Clinics of pediatric dentistry department.
SUBJECTS AND METHODS:
Healthy Saudi children 6–12 years old with no known allergies were screened for eligibility between May and December 2019.
A single investigator collected saliva samples.
The
MTHFR
C677T and A1298C polymorphisms were analyzed using polymerase chain reaction and restriction fragment length polymorphism.
MAIN OUTCOME MEASURE:
The prevalence of
MTHFR
gene variants (C677T and A1298C) among the subjects.
SAMPLE SIZE:
138.
RESULTS:
MTHFR
C677T polymorphism was present in 36.
2% of the sample and 90.
0% of children carrying this allele were heterozygotes.
MTHFR
A1298C polymorphism was present in 91.
3% of the sample and 77.
0% of the children carrying this allele were heterozygotes.
No linkage disequilibrium between
MTHFR
C677T and
MTHFR
A1298C was observed within this sample.
CONCLUSIONS:
Our study found a high frequency of the
MTHFR
A1298C genotype, which was substantially more abundant than expected based on a Hardy-Weinberg distribution.
Therefore, caution is advised in using N
2
O in Saudi children as the increased prevalence of this
MTHFR
allele may increase the incidence of serious adverse effects among these children.
LIMITATIONS:
Further studies are recommended with a larger sample size from randomly selected hospitals from different regions of Saudi Arabia.
CONFLICT OF INTEREST:
None.
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