Factor Information
Data ID 495
Factor frequencies of MTHFR gene 677 TT genotype in the mothers
Description The frequency of the MTHFR gene 677 TT polymorphism in the mothers who had offspring with TOF was significantly higher than that in the non-CHD controls (P<0.05).
Biomarker NA
Classification D1 (molecular factor - DNA)
Association
Application risk assessment
Objective offspring CHD risk
p Value 0.0033
OR 2.93
Conclusion A significant interaction was found between the homozygous 677 T/T MTHFR gene in children and the maternal occupational status and level of drug exposure during gestation. Avoiding or reducing the exposure of the risk factors mentioned above, strengthening pre-pregnancy checkups and guidance might help to reduce the risk of CHD
Risk Factor risk factor
CHD Type
ID 53
CHD Type isolated CHD
CHD Subtype TOF
Reference
PMID 29600076
Year 2018
Title Risk factors and methylenetetrahydrofolate reductase gene in congenital heart disease.
Sample
Population mothers
Source interview
Region Beijing, China
Method The MTHFR genotype was analyzed by RFLP.Interactions between environmental risk factors and MTHFR gene polymorphisms were evaluated by the RERI, the attributable proportion due to interaction (AP), and the synergy index (S).
Race Asian
Disease History N/A
Treatment History N/A
Group the mothers who had offspring with TOF(Treatment) the mother of the children with non-CHD(Control)
Number 18(total:41) 50(total:237)
Age ≤20 years 20 (5.8%); 21–34 years 254 (73.4%); ≥35 years 72 (20.8). ≤20 years 12 (5.1%); 21–34 years 182 (76.8%); ≥35 72 years 43 (18.1%)
Gender (Male: Female) 0:18 0:50
Marker Level 0.439 0.211