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Cardiovascular Programming During and After Diabetic Pregnancy: Role of Placental Dysfunction and IUGR
Immaculate M Langmia1,2,3, Kristin Kräker1,2,4,5,6, Sara E Weiss1,2,4
1Experimental and Clinical Research Center, A Joint Cooperation Between the Max-Delbrueck Center for Molecular Medicine and the Charité Universitätsmedizin Berlin, Berlin, Germany.
Insights
Intrauterine growth restriction (IUGR) can lead to fetal malnutrition and hypoxia, causing epigenetic changes. These in utero modifications can program cardiovascular disease later in life, impacting adult health.
Area of Science:
- Developmental Biology
- Cardiovascular Science
- Neonatal Health
Background:
- Intrauterine growth restriction (IUGR) affects fetal development, leading to significant neonatal mortality and morbidity.
- Maternal factors like uncontrolled diabetes can cause placental dysfunction, resulting in IUGR and fetal malnutrition.
- IUGR-induced fetal adaptation involves epigenetic modifications, programming long-term health outcomes, including cardiovascular disease.
Purpose of the Study:
- To systematically review the molecular mechanisms of IUGR in cardiovascular programming.
- To explore the role of in utero epigenetic modifications in adult cardiovascular disease development.
- To discuss animal models and experimental evidence of IUGR's long-term fetal programming effects.
Main Methods:
- Systematic review of molecular mechanisms in IUGR pathogenesis.
- Analysis of animal models using nutrient restriction and hypoxia.
- Inclusion of experimental evidence on long-term fetal programming.
Main Results:
- Placental dysfunction in IUGR leads to fetal undernutrition and hypoxia.
- Adverse in utero conditions trigger epigenetic modifications in the fetus.
- These epigenetic changes contribute to cardiovascular programming and disease risk.
Conclusions:
- IUGR has profound, long-lasting effects on cardiovascular health through epigenetic programming.
- Understanding these mechanisms is crucial for identifying susceptible individuals.
- Development of targeted preventive and therapeutic strategies for IUGR is needed.
Abstract:
Intrauterine growth restriction (IUGR) is a condition whereby a fetus is unable to achieve its genetically determined potential size. IUGR is a global health challenge due to high mortality and morbidity amongst affected neonates. It is a multifactorial condition caused by maternal, fetal, placental, and genetic confounders. Babies born of diabetic pregnancies are usually large for gestational age but under certain conditions whereby prolonged uncontrolled hyperglycemia leads to placental dysfunction, the outcome of the pregnancy is an intrauterine growth restricted fetus with clinical features of malnutrition. Placental dysfunction leads to undernutrition and hypoxia, which triggers gene modification in the developing fetus due to fetal adaptation to adverse utero environmental conditions. Thus, in utero gene modification results in future cardiovascular programming in postnatal and adult life. Ongoing research aims to broaden our understanding of the molecular mechanisms and pathological pathways involved in fetal programming due to IUGR. There is a need for the development of effective preventive and therapeutic strategies for the management of growth-restricted infants. Information on the mechanisms involved with in utero epigenetic modification leading to development of cardiovascular disease in adult life will increase our understanding and allow the identification of susceptible individuals as well as the design of targeted prevention strategies. This article aims to systematically review the latest molecular mechanisms involved in the pathogenesis of IUGR in cardiovascular programming. Animal models of IUGR that used nutrient restriction and hypoxia to mimic the clinical conditions in humans of reduced flow of nutrients and oxygen to the fetus will be discussed in terms of cardiac remodeling and epigenetic programming of cardiovascular disease. Experimental evidence of long-term fetal programming due to IUGR will also be included.
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