Corticotrophin releasing hormone and the timing of birth
Roger Smith1, Richard C Nicholson
1Mothers and Babies Research Centre, Hunter Medical Research Institute, John Hunter Hospital, University of Newcastle, NSW 2310, Australia. roger.smith@newcastle.edu.au
Insights
Corticotrophin-releasing hormone (CRH) from the placenta regulates fetal development and delivery timing. Elevated maternal CRH levels may predict preterm labor, suggesting its role in a placental clock.
Area of Science:
- Reproductive biology
- Endocrinology
- Obstetrics
Background:
- Corticotrophin-releasing hormone (CRH) is a key hypothalamic peptide regulating the stress response via the pituitary-adrenal axis.
- CRH is abundantly expressed in the human placenta, with high concentrations in maternal and fetal plasma during late pregnancy.
Purpose of the Study:
- To review the current evidence on the role of placental CRH in human parturition.
- To explore CRH's involvement in fetal maturation, delivery timing, and fetal-placental blood flow.
Main Methods:
- Literature review of studies investigating CRH in pregnancy and parturition.
- Analysis of clinical data on maternal plasma CRH concentrations in relation to delivery timing.
Main Results:
- Placental CRH is implicated in regulating fetal maturation and the timing of delivery.
- Elevated CRH concentrations are observed in patients experiencing preterm labor.
- CRH increase patterns correlate with delivery timing, suggesting a placental clock mechanism.
Conclusions:
- Maternal plasma CRH levels may serve as a clinical marker for identifying women at high risk of preterm delivery.
- CRH antagonists show potential for preventing preterm labor.
- Future research must consider the species-specific nature of CRH in parturition, as significant placental production is primate-specific.
Abstract:
Corticotrophin-releasing hormone (CRH) is the hypothalamic peptide that controls the function of the pituitary-adrenal axis in response to stress. CRH is also expressed abundantly in the human placenta and is present in high concentrations in maternal and fetal plasma during late pregnancy. During pregnancy, CRH derived from the placenta is thought to play a crucial role in the regulation of fetal maturation and the timing of delivery, and CRH has also been implicated in the control of fetal-placental blood flow. Elevated CRH concentrations, as compared with gestational age matched controls, occur in patients in preterm labour. The exponential curve depicting the CRH increase is shifted to the left in women who will subsequently deliver preterm and to the right in women who will deliver post dates. This has led to the suggestion that CRH production is linked to a placental clock which determines the length of gestation. Clinically, maternal plasma CRH concentrations may be useful in identifying women at high risk of preterm delivery and CRH antagonists may be useful in preventing preterm labour. As significant CRH production by the placenta is restricted to primates, future research must take into account the species specificity of the mechanisms regulating parturition. A number of significant gaps remain in our knowledge of the function of this peptide in pregnancy. This review examines the current evidence regarding the role of CRH in human parturition.
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