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Published on: August 25, 2014
Fetal exposure to placental corticotropin-releasing hormone is associated with child self-reported internalizing
Mariann A Howland1, Curt A Sandman1, Laura M Glynn2
1Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA.
Insights
Elevated prenatal exposure to placental corticotropin-releasing hormone (pCRH) is linked to increased internalizing symptoms in children by age 5. Maternal cortisol levels during pregnancy did not show a significant association with these symptoms.
Area of Science:
- Neuroscience
- Developmental Psychology
- Endocrinology
Background:
- Prenatal exposure to maternal stress hormones like cortisol can impact fetal nervous system development, increasing the risk for later internalizing symptoms.
- Placental corticotropin-releasing hormone (pCRH) acts as a feto-placental stress signal, potentially offering a more direct measure of the fetal stress experience.
- The long-term programming effects of pCRH on child development remain largely unknown.
Purpose of the Study:
- To investigate the association between prenatal exposure to maternal cortisol and placental corticotropin-releasing hormone (pCRH).
- To examine the relationship between these prenatal stress hormone exposures and child self-reported internalizing symptoms at age 5.
Main Methods:
- Maternal plasma cortisol and pCRH levels were measured across multiple gestational points (15, 19, 25, 31, and 36 weeks).
- Child internalizing symptoms at age 5 were assessed using the Berkeley Puppet Interview.
- The study included 83 women and 91 children, with measurements taken from full-term births.
Main Results:
- Elevated placental corticotropin-releasing hormone (pCRH) profiles during mid-gestation were significantly associated with higher levels of child internalizing symptoms at age 5.
- This association remained significant after controlling for obstetric risk, maternal psychological state, and socioeconomic status.
- Prenatal maternal cortisol levels were not found to be significantly associated with child internalizing symptoms at age 5.
Conclusions:
- Elevated exposure to the feto-placental stress signal, pCRH, appears to have programming effects on the developing fetal central nervous system.
- These programming effects can lead to lasting consequences for child mental health, specifically manifesting as internalizing symptoms.
- The findings highlight pCRH as a critical factor in fetal neurodevelopment and subsequent child psychological well-being.
Objective:
Fetal exposure to maternal prenatal stress hormones such as cortisol exerts influences on the developing nervous system that persist and include risk for internalizing symptoms later in life. Placental corticotropin-releasing hormone (pCRH) is a feto-placental stress signal that also shapes fetal neurodevelopment and may be a more direct indicator of the fetal experience than maternal stress hormones. The programming effects of pCRH on child development are unknown. The current investigation examined associations between prenatal maternal and placental stress hormone exposures (maternal cortisol and pCRH) and child self-reported internalizing symptoms at age 5.
Method:
Maternal plasma cortisol and pCRH levels were measured at 15, 19, 25, 31, and 36 weeks' gestation in a sample of 83 women and their 91 children (8 sibling pairs from separate pregnancies), who were born full-term. Child self-reported internalizing symptoms at age 5 were obtained using scales of the Berkeley Puppet Interview.
Results:
Placental CRH profiles (including elevations in mid-gestation) were associated with higher levels of internalizing symptoms at age 5. This effect was not explained by critical prenatal or postnatal influences, including obstetric risk, concurrent maternal psychological state, and family socio-economic status. Prenatal maternal cortisol was not significantly associated with child self-reported internalizing symptoms.
Conclusions:
Findings suggest that elevated exposures to the feto-placental stress signal pCRH exert programming effects on the developing fetal central nervous system, with lasting consequences for child mental health.
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