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Sex Differences in Offspring of Preeclamptic Pregnancies
Nathan Campbell1, Dylan Solise2, Evangeline Deer1
1Department of Pharmacology & Toxicology, University of Mississippi Medical Center, Jackson, MS.
Insights
Adverse pregnancy conditions like preeclampsia can lead to fetal growth restriction (FGR), increasing offspring
Area of Science:
- Reproductive biology and developmental programming
- Immunology and inflammation in pregnancy
- Neurovascular and cardiovascular health in offspring
Background:
- Poor uterine environments and fetal growth restriction (FGR) are linked to long-term offspring health issues, including cardiovascular and neurological diseases.
- Preeclampsia (PE), a hypertensive pregnancy disorder, is characterized by inflammation and often results in FGR and preterm birth.
- Existing research highlights sex differences in adult cardiovascular disease risk but less so for neurological disorders following PE pregnancies.
Purpose of the Study:
- To review current research on sex differences in developmental programming of hypertension and neurological disorders after preeclampsia.
- To address knowledge gaps regarding the immune system's role in FGR offspring developing hypertension or neurovascular disorders.
- To examine the impact of sex on long-term health outcomes following adverse pregnancy conditions.
Main Methods:
- Literature review of epidemiological studies and experimental models.
- Analysis of research investigating the link between fetal exposure and adult disease.
- Focus on studies examining sex-specific effects and immune system involvement.
Main Results:
- Fetal exposure to adverse conditions, including PE, predisposes offspring to hypertension and neurological issues.
- PE involves chronic inflammation and immune dysregulation.
- Sex of the offspring influences the development of cardiovascular and potentially neurological diseases later in life.
Conclusions:
- Understanding sex differences is crucial for comprehending the long-term health consequences of PE and FGR.
- Further research is needed on the immune system's role and sex-specific therapeutic strategies.
- Developmental programming following PE impacts offspring health, with potential sex-based variations.
Abstract:
A poor uterine environment causes changes in fetal development that affect the health of offspring long-term. Although there are multiple pathways that contribute to the development of cardiovascular and neurological disease, low birth weight or fetal growth restriction (FGR) predisposes offspring to these diseases. There is a link between fetal exposure to adverse influences and hypertension later in life. Many epidemiological studies support the link between fetal life and the risk of disease later in life. Experimental models have sought to provide mechanistic proof of this link while simultaneously investigating potential therapeutics or treatment pathways. Preeclampsia (PE), one of several hypertensive disorders in pregnancy, is a leading cause of morbidity and mortality for both the mother and fetus. Studies have shown that PE is a state of chronic inflammation and there is an imbalance between pro-inflammatory and regulatory immune cells and mediators. There is no cure for PE beyond the delivery of the fetal-placental unit, and many PE pregnancies result in FGR and preterm birth. Epidemiological data demonstrate that the sex of the offspring is correlated with the degree of cardiovascular disease that develops with the age of the offspring yet few studies examine the effect of sex on the development of neurological disorders. Even fewer studies examine the effects of therapeutics on offspring of different genders following a PE pregnancy. Moreover, there remain significant gaps in knowledge concerning the role the immune system plays in FGR offspring developing hypertension or neurovascular disorders later in life. Therefore, the purpose of this review is to highlight current research on sex differences in the developmental programming of hypertension and neurological disorders following a PE pregnancy.
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