Factor Information
Data ID 1692
Factor SNPs in children: MTHFR gene rs1801131:AA
Description Logistic regression analyses adjusted for gender of children, occupation of mothers, family history with CHD, history of abortion, history of adverse pregnancy, early pregnancy health, fetus during pregnancy, pesticide exposure and drug exposure
Biomarker NA
Classification D1 (molecular factor - DNA)
Association
Application risk assessment
Objective The aim of this study is to evaluate the relevant risk-factors of children with CHD and their mothers.
OR 1
Conclusion After adjustment for gender of children, occupation of mother, family history with CHD, history of abortion, history of adverse pregnancy, early preg- nancy health, fetus during pregnancy, pesticide exposure and drug exposure, only rs1801131 (A vs. C) variant genotypes significantly increased host CHD risk, when compared with children without CHD (OR = 1.42, 95% CI = 1.00–2.44 in additive model)
Risk Factor unknown
CHD Type
ID 148
CHD Type NA
CHD Subtype NA
Reference
PMID 26035828
Year 2015
Title Study on Environmental Causes and SNPs of MTHFR, MS and CBS Genes Related to Congenital Heart Disease
Sample
Population children
Source questionnaire
Region Nanjing, China
Method logistic regression analyses adjusted for gender of children, occupation of mothers, family history with CHD, history of abortion, history of adverse pregnancy, early pregnancy health, fetus during pregnancy, pesticide exposure and drug exposure
Race Asian
Disease History History of CHD/abortion/adverse pregnancy
Treatment History N/A
Group CHD children(Treatment) control children(Control)
Number 74 163
Age N/A N/A
Gender (Male: Female) N/A N/A
Marker Level 74(53.63%) 163(80.20%)