Behavioural dysfunctions of 10-year-old children born extremely preterm associated with corticotropin-releasing

Alan Leviton1, Elizabeth N Allred1, Robert M Joseph2

  • 1Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Insights

Placental corticotropin-releasing hormone (CRH) levels did not predict later school dysfunctions in extremely preterm children. However, high placental CRH was linked to social limitations in girls.

Area of Science:

  • Reproductive biology
  • Developmental neuroscience
  • Pediatric health

Background:

  • Extremely preterm (EP) birth poses risks for neurodevelopmental outcomes.
  • Corticotropin-releasing hormone (CRH) plays a role in stress response and development.
  • Placental CRH may influence fetal development and long-term health.

Purpose of the Study:

  • To investigate the association between placental corticotropin-releasing hormone (CRH) expression and school-related dysfunctions in children born extremely preterm (EP).
  • To determine if CRH mRNA levels in the placenta predict neurodevelopmental and behavioral outcomes at age 10.

Main Methods:

  • Placental CRH mRNA expression was quantified in 761 EP children.
  • Children underwent comprehensive neurodevelopmental and behavioral assessments at age 10.
  • Statistical analyses examined associations between extreme CRH mRNA quartiles and adverse assessment scores.

Main Results:

  • Overall, no significant association was found between the highest or lowest placental CRH mRNA quartiles and increased risks of school-related dysfunctions.
  • A notable finding was that seven indicators of social limitations were associated with the highest quartile of placental CRH mRNA in girls.
  • Adjustments for delivery indications minimally altered these findings.

Conclusions:

  • Placental CRH mRNA levels, in isolation, do not appear to be a strong predictor of general school-related dysfunctions in EP children at age 10.
  • Specific to girls, elevated placental CRH expression may be linked to an increased risk of social challenges.
  • Further research is needed to understand the nuanced role of CRH in sex-specific developmental trajectories following EP birth.
Abstract

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