Maternal and cord blood homocysteine, vitamin B12, folate, and B-type natriuretic peptide levels at term for predicting congenital heart disease of the neonate: a case …

N Sahin-Uysal, C Gulumser, E Kocaman… - … Journal of Maternal …, 2020 - Taylor & Francis
maternal intake of folic acid reduces the risk of CHD [Citation15–17], multiple studies have
focused on identifying genetic and metabolic risk factors of … that hyperhomocysteinemia during …

Association of maternal dietary intakes and CBS gene polymorphisms with congenital heart disease in offspring

Y Li, J Diao, J Li, L Luo, L Zhao, S Zhang… - … Journal of Cardiology, 2021 - Elsevier
… So mutation of CBS gene impairs the stability of enzyme and decreases the catalytic activity
[39], leading to accumulation of hcy in the body and the hyperhomocysteinemia (HHcy). In …

Association of Maternal Betaine-Homocysteine Methyltransferase (BHMT) and BHMT2 Genes Polymorphisms with Congenital Heart Disease in Offspring

M Luo, T Wang, P Huang, S Zhang, X Song, M Sun… - Reproductive …, 2023 - Springer
… levels of Hcy is a known risk factor for human diseases. Kilmer reviewed the chemical …
population-based studies that maternal hyperhomocysteinemia was significantly associated with …

Environmental risk factors for congenital heart disease

JI Kalisch-Smith, N Ved… - Cold Spring Harbor …, 2020 - cshperspectives.cshlp.org
Hyperhomocysteinemia (HHcy) can be caused by dietary deficiencies in folic acid, vitamin
B6, and/or vitamin B12; … Congenital heart disease in maternal phenylketonuria: report from the …

Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study

X Song, Q Li, J Diao, J Li, Y Li, S Zhang, L Zhao… - BMC Pregnancy and …, 2022 - Springer
congenital heart disease (CHD). This study examined the role of MTHFD1 gene and maternal
smoking on infant CHD risk… likely shared some etiologic and specifically genetic risk factors

Methyltetrahydrofolate-homocysteine methyltransferase reductase gene and congenital heart defects in Down syndrome

J Vraneković, G Slivšek… - …, 2020 - unirepository.svkri.uniri.hr
… to examine maternal risk factors for CHD, two groups of mothers were compared; mothers of
… Statistically significant differences in the incidence of congenital heart defects with respect to …

Study on maternal SNPs of MTHFR gene and HCY level related to congenital heart diseases

H Shi, S Yang, N Lin, P Huang, R Yu, M Chen… - … Cardiology, 2021 - Springer
factors, our results suggested that the maternal MTHFR rs1801133 polymorphism might be
a risk factor of their … factor of offspring CHDs due to the hyperhomocysteinemia by abnormal …

Folic acid intake in prevention of congenital heart defects: A mini evidence review

Z Soheilirad - Clinical nutrition ESPEN, 2020 - Elsevier
… and role of folic acid in ameliorating hyperhomocysteinemia [1]. Since folic acid as a crucial
… up hyperhomocysteinemia [6]. A positive correlation exists between the levels of maternal

… Methylation biomarkers S-adenosylmethionine and S-adenosylhomocysteine and methylation potential in newborns with congenital heart disease and their mothers

D Ninković, K Fumić, IB Kuš, T Kapić, I Križić… - 2021 - adc.bmj.com
mother’s hyperhomocysteinemia are associated with the risk of having a child with congenital
heart disease… homocysteine itself is a risk factor for congenital heart disease or changes in …

Homocysteine: its possible emerging role in at-risk population groups

E Azzini, S Ruggeri, A Polito - International journal of molecular sciences, 2020 - mdpi.com
… genetic causes of severe hyperhomocysteinemia, associated with … subjects and concluded
that mothers with NTD offspring had … biomarkers in children with congenital heart diseases. …