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Copyright Reserved. Designated trademarks and brands are the property of their owners.Use of this web site constitutes acceptance of the terms of use and privacy policy.Juho Nurm is a human geneticist and the director of the Human Heredity and Health Program at the University of Helsinki.

The findings of a genome-wide association study suggest that variation in a very short DNA sequence – less than 200 letters long – may be linked to increased or decreased risk of developing ADHD, one of the most common mental health conditions in children.

“The results are very promising, but we do not know yet which of the SNPs most likely contribute to risk for ADHD,” Nurm said.

“The findings have to be confirmed in several other studies, before we can say that these SNPs are the basis for pharmacological treatment,” he added.

ADHD is a common chronic disorder of childhood. Symptoms include uncontrollable moving and constant talking or excessive talking, which is not related to the context of a situation.

“The findings of this study suggest that there are genetic factors that have an influence on the course of ADHD,” said Jan Höglund, one of the researchers.

“These are probably not as strong as other, environmental factors. The main component in relation to this study is the role of genetics,” Höglund explained.

Children with ADHD suffer from problems with thinking, feelings, behaviour, social skills and academic and occupational outcomes. For example, they often have trouble keeping their attention on tasks.

“The findings are not surprising, but this is a very important study,” said Björn R. Karimi, a professor in child psychiatry at the Karolinska Institutet in Stockholm.

“ADHD is a complex disorder and most symptoms are influenced by genes and the environment. Finding genetic factors may enable us to diagnose the disorder earlier,” he added.

The research was published in the British Journal of Psychiatry.S

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