Javascript must be enabled to continue!
Prevalence of methylenetetrahydrofolate reductase gene polymorphisms (C677T, and A1298C) among Saudi children receiving dental treatment
View through CrossRef
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.
Related Results
Study of the Association between MTHFR Polymorphism (rs1801133) and the Outcome of Methotrexate Treatment in Rheumatoid Arthritis Patient
Study of the Association between MTHFR Polymorphism (rs1801133) and the Outcome of Methotrexate Treatment in Rheumatoid Arthritis Patient
Abstract
Background
Rheumatoid arthritis is a chronic systemic autoimmune disease that causes loss of joint function and signifi...
Awareness of Dental Personnel towards Occupational Injury- A Cross Sectional Study
Awareness of Dental Personnel towards Occupational Injury- A Cross Sectional Study
TITLE:
Awareness of dental personnel towards occupational injury- a cross sectional study
ABSTRACT
Objective: To determine the awareness of dental personnel towards dental occup...
PREVALENCE AND DIET HABIT AS DETERMINANT OF DENTAL CARIES AMONG CHILDREN ATTENDING THE DIFFERENT PRIMARY HEALTH CARE CENTERS OF ALAHSA REGION OF SAUDI ARABIA
PREVALENCE AND DIET HABIT AS DETERMINANT OF DENTAL CARIES AMONG CHILDREN ATTENDING THE DIFFERENT PRIMARY HEALTH CARE CENTERS OF ALAHSA REGION OF SAUDI ARABIA
Background: Dental caries, a chronic infectious resulting from tooth-adherent cariogenic bacteria is a the oldest and the most common disorder
reported so far. Studies suggest that...
Guest Editorial
Guest Editorial
Dental caries is one of the major health problems in Indonesia. Data from Indonesian Basic Health Research in 2013, 2015 and 2018 showed a consistent increase in the prevalence of ...
Influence of MTHFR C677T and A1298C polymorphisms on the survival of pediatric patients with non-Hodgkin lymphoma
Influence of MTHFR C677T and A1298C polymorphisms on the survival of pediatric patients with non-Hodgkin lymphoma
Objective: We investigated the influence of methylenetetrahydrofolate
reductase (MTHFR) C677T/A1298C polymorphisms on the survival of
pediatric non-Hodgkin lymphoma (NHL) cases in ...
Frequency of methylenetetrahydrofolate reductase C677T polymorphism in patients with cardiovascular disease in Eastern Saudi Arabia
Frequency of methylenetetrahydrofolate reductase C677T polymorphism in patients with cardiovascular disease in Eastern Saudi Arabia
OBJECTIVE: Homozygosity for the C677T mutation in the gene of the thermolabile enzyme 5,10 methylenetetrahydrofolate reductase (MTHFR) associates with reduced enzyme activity, lead...
Role of Thrombotic Risk Factors in End-Stage Renal Disease
Role of Thrombotic Risk Factors in End-Stage Renal Disease
Introduction: Genetic polymorphisms that are found among factors of the coagulation cascade are factor V leiden mutation (FVL), prothrombin (PT), and methylenetetrahydrofolate redu...
AMPD1 and MTHFR genes are not associated with calcium levels in rheumatoid arthritis patients with methotrexate therapy in Indonesia
AMPD1 and MTHFR genes are not associated with calcium levels in rheumatoid arthritis patients with methotrexate therapy in Indonesia
AbstractRheumatoid Arthritis (RA) is a chronic and progressive autoimmune disease that affects synovial tissues has greater risk of developing secondary osteoporosis (OP). In parti...

