Scientist have identified a link between exposure to high levels of oestrogen sex hormones in the womb and the likelihood of developing autism. The findings are published today in the journal Molecular Psychiatry.
The discovery adds further
evidence to support the prenatal sex steroid theory of autism first proposed 20
years ago.
In 2015, a team of scientists
at the University of Cambridge and the State Serum Institute in Denmark
measured the levels of four prenatal steroid hormones, including two known as
androgens, in the amniotic fluid in the womb and discovered that they were
higher in male foetuses who later developed autism. These androgens are
produced in higher quantities in male than in female foetuses on average, so
might also explain why autism occurs more often in boys. They are also known to
masculinise parts of the brain, and to have effects on the number of
connections between brain cells.
Today, the same scientists have
built on their previous findings by testing the amniotic fluid samples from the
same 98 individuals sampled from the Danish Biobank, which has collected
amniotic samples from over 100,000 pregnancies, but this time looking at
another set of prenatal sex steroid hormones called oestrogens. This is an
important next step because some of the hormones previously studied are
directly converted into oestrogens.
All four oestrogens were
significantly elevated, on average, in the 98 foetuses who later developed
autism, compared to the 177 foetuses who did not. High levels of prenatal
oestrogens were even more predictive of likelihood of autism than were high
levels of prenatal androgens (such as testosterone). Contrary to popular belief
that associates oestrogens with feminisation, prenatal oestrogens have effects
on brain growth and also masculinise the brain in many mammals.
Professor Simon Baron-Cohen,
Director of the Autism Research Centre at the University of Cambridge, who led
this study and who first proposed the prenatal sex steroid theory of autism,
said: "This new finding supports the idea that increased prenatal sex
steroid hormones are one of the potential causes for the condition. Genetics is
well established as another, and these hormones likely interact with genetic
factors to affect the developing foetal brain."
Alex Tsompanidis, a PhD student
in Cambridge who worked on the study, said: "These elevated hormones could
be coming from the mother, the baby or the placenta. Our next step should be to
study all these possible sources and how they interact during pregnancy."
Dr Alexa Pohl, part of the
Cambridge team, said: "This finding is exciting because the role of
oestrogens in autism has hardly been studied, and we hope that we can learn
more about how they contribute to foetal brain development in further experiments.
We still need to see whether the same result holds true in autistic
females."
However, the team cautioned
that these findings cannot and should not be used to screen for autism.
"We are interested in understanding autism, not preventing it," added
Professor Baron-Cohen.
Dr Arieh Cohen, the biochemist
on the team, based at the State Serum Institute in Copenhagen, said: "This
is a terrific example of how a unique biobank set up 40 years ago is still
reaping scientific fruit today in unimagined ways, through international
collaboration."
The research was supported by
the Autism Research Trust, the Medical Research Council, and Wellcome.
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