Children born to older fathers are at increased risk of having an
autistic spectrum disorder (ASD), according to
new
research published in the October issue of the
British
Journal of Psychiatry.
But the researchers found no link between
increased maternal age and the risk of ASD.
The study, which was carried out in Japan,
involved 84 participants with ‘high-functioning’ ASD. This meant
that they displayed symptoms of autism, such as difficulties with
socialising, communication and behaviour, but did not have an
intellectual disability (i.e. all the participants had an IQ of
more than 70).
This group was compared with 208 healthy
controls, who had no intellectual disability and had not been
diagnosed with any psychiatric disorder.
The participants were divided into three
groups, depending on how old their parents were when they were
born. The three age classes were: under 29, 29-32 and over 33.
The researchers found that a one-level advance
in the paternal age class corresponded to a 1.8-fold increase in
the risk of the child having high-functioning ASD. However, there
was no association between an increase in the maternal age at birth
and the development of ASD.
Explanations for the effect are unclear, but
it is thought that mutations can occur in the paternal germ line as
the father gets older. Mutations in sperm can then be passed on to
children.
This is the first study to explore the effect
of paternal age on the risk of high-functioning ASD. Its findings
correspond with previous studies which have shown a link between
older fathers and a low IQ in children.
For further information, please contact Liz Fox or Deborah
Hart in the Communications Department.
Telephone: 020 7235 2351 Extensions. 6298 or 6127
References:
Tsuchiya K, Matsumoto K, Miyachi T, Tsujii M, Nakamura K, Takagai S, Kawai M, Yagi A, Iwaki K, Suda S, Sugihara G, Iwata Y, Matsuzaki H, Sekine Y, Suzuki K, Sugiyama T, Mori N and Takei N (2008) Paternal age at birth and high-functioning autistic-spectrum disorder in offspring, British Journal of Psychiatry, 193: 316-321