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Published on: May 5, 2018
Increased Fetal Cardiovascular Disease Risk: Potential Synergy Between Gestational Diabetes Mellitus and Maternal
Cristian Espinoza1, Barbara Fuenzalida2, Andrea Leiva3
1Faculty of Biological Sciences, Pontificia Universidad Catolica de Chile, Santiago 8330024, Chile.
Insights
Maternal metabolic diseases like gestational diabetes and high cholesterol during pregnancy may increase fetal cardiovascular disease risk. These conditions can synergistically harm placental function and fetal development.
Area of Science:
- Obstetrics and Gynecology
- Cardiology
- Developmental Biology
Background:
- Cardiovascular diseases (CVD) are a leading global cause of death.
- Maternal metabolic conditions, including gestational diabetes mellitus (GDM) and maternal supraphysiological hypercholesterolemia (MSPH), are linked to increased fetal CVD risk.
- GDM involves hyperglycemia, inflammation, and insulin resistance, impacting fetal nutrient exposure and endothelial function.
- MSPH is characterized by elevated cholesterol, leading to endothelial dysfunction and altered fetal nutrient transport.
Purpose of the Study:
- To explore the cellular mechanisms linking maternal metabolic diseases to fetal cardiovascular disease risk.
- To investigate the combined effects of GDM and MSPH on placental function and fetal development.
- To highlight the need for further research into the separate and cumulative roles of GDM and MSPH.
Main Methods:
- This study is a review of existing evidence and a theoretical exploration of cellular processes.
- Analysis of the impact of GDM and MSPH on placental nutrient transport and endothelial function.
- Examination of the potential synergistic effects of co-occurring GDM and MSPH.
Main Results:
- Both GDM and MSPH independently impair endothelial vascular tone and alter nutrient transport to the fetus.
- The simultaneous occurrence of GDM and MSPH may synergistically exacerbate placental dysfunction and endothelial damage.
- Current understanding of the cellular processes underlying these associations, especially in combination, is limited.
Conclusions:
- Maternal GDM and MSPH represent significant risk factors for fetal cardiovascular health.
- The combined presence of GDM and MSPH may pose a synergistic threat to fetal cardiovascular development.
- Further research is crucial to elucidate the specific cellular pathways involved and to develop targeted interventions.
Abstract:
Cardiovascular diseases (CVD) remain a major cause of death worldwide. Evidence suggests that the risk for CVD can increase at the fetal stages due to maternal metabolic diseases, such as gestational diabetes mellitus (GDM) and maternal supraphysiological hypercholesterolemia (MSPH). GDM is a hyperglycemic, inflammatory, and insulin-resistant state that increases plasma levels of free fatty acids and triglycerides, impairs endothelial vascular tone regulation, and due to the increased nutrient transport, exposes the fetus to the altered metabolic conditions of the mother. MSPH involves increased levels of cholesterol (mainly as low-density lipoprotein cholesterol) which also causes endothelial dysfunction and alters nutrient transport to the fetus. Despite that an association has already been established between MSPH and increased CVD risk, however, little is known about the cellular processes underlying this relationship. Our knowledge is further obscured when the simultaneous presentation of MSPH and GDM takes place. In this context, GDM and MSPH may substantially increase fetal CVD risk due to synergistic impairment of placental nutrient transport and endothelial dysfunction. More studies on the separate and/or cumulative role of both processes are warranted to suggest specific treatment options.
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