Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms

Madhumita Basu1,2, Vidu Garg1,2,3

  • 1Center for Cardiovascular Research and Heart Center, Nationwide Children's Hospital, Columbus, Ohio.

Birth Defects Research
|December 22, 2018
PubMed

Insights

Maternal diabetes mellitus (matDM) is a risk factor for congenital heart disease (CHD). Research explores how maternal hyperglycemia affects embryonic heart development to find prevention strategies for CHD.

Area of Science:

  • Cardiology
  • Developmental Biology
  • Genetics

Background:

  • Congenital heart disease (CHD) is a common birth defect with multifactorial etiology.
  • Genetic factors are increasingly identified, but environmental contributions remain unclear.
  • Maternal diabetes mellitus (matDM) is a known risk factor for CHD, yet mechanisms are elusive.

Purpose of the Study:

  • To explore the link between maternal diabetes mellitus and congenital heart disease.
  • To review cellular and molecular pathways affected by maternal hyperglycemia during embryonic heart development.
  • To discuss potential prevention strategies for CHD in high-risk populations.

Main Methods:

  • Review of epidemiological data linking matDM and CHD.
  • Discussion of animal models used to study matDM's impact on cardiac development.
  • Analysis of cellular and molecular pathways affected by maternal hyperglycemia.

Main Results:

  • Maternal hyperglycemia impacts numerous cellular and molecular pathways in the developing heart.
  • Animal models provide insights into the mechanisms linking matDM to cardiac malformations.
  • Understanding these mechanisms is crucial for developing prevention strategies.

Conclusions:

  • Elucidating the mechanisms by which maternal diabetes mellitus causes congenital heart disease is critical.
  • This knowledge can lead to novel prevention strategies for CHD in offspring of diabetic mothers.
  • Further research into environmental factors like matDM is needed to reduce CHD incidence.

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