Sex differences in placenta-derived markers and later autistic traits in children

A Tsompanidis1, L Blanken2,3, Z A Broere-Brown2,4

  • 1Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK. at768@medschl.cam.ac.uk.

PubMed

Insights

Higher placental growth factor (PlGF) in the second trimester is linked to being male and increased autistic traits. This suggests a potential role for PlGF in sex differences observed in autism spectrum disorder development.

Area of Science:

  • Reproductive biology
  • Developmental neuroscience
  • Autism research

Background:

  • Autism spectrum disorder (ASD) is more prevalent in males, who also tend to exhibit higher levels of autistic traits.
  • Fetal sex significantly influences placental function, but the connection to postnatal autistic traits remains unclear.

Purpose of the Study:

  • To investigate the association between placental function markers and sex differences in autistic traits.
  • To examine placental growth factor (PlGF) and soluble fms-like tyrosine kinase (sFlt-1) levels in relation to autistic traits in offspring.

Main Methods:

  • Maternal plasma concentrations of PlGF and sFlt-1 were measured during the first and second trimesters.
  • Autistic traits in 6-year-old children were assessed using the Social Responsiveness Scale (SRS).
  • Sex-stratified regression models analyzed associations between placental markers and autistic traits, controlling for covariates.

Main Results:

  • sFlt-1 levels were lower in male pregnancies but not associated with autistic traits.
  • PlGF levels differed by fetal sex, being lower in the first trimester and higher in the second trimester for males.
  • Higher second-trimester PlGF and a faster rate of PlGF increase were associated with higher autistic traits, particularly in males.

Conclusions:

  • Second-trimester PlGF levels and their rate of increase are associated with both male sex and higher autistic traits.
  • PlGF may partially mediate the observed sex differences in autistic traits, highlighting its potential role in neurodevelopmental trajectories.

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