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P01-364 Associations of 5HTT-LPR with ADHD symptoms are moderated by platelet MAOB activity

Published online by Cambridge University Press:  16 April 2020

H.-L. Wargelius
Affiliation:
Neuroscience, Uppsala University, Uppsala, Stockholm, Sweden
K. Malmberg
Affiliation:
Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden
J.-O. Larsson
Affiliation:
Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden
L. Oreland
Affiliation:
Neuroscience, Uppsala University, Uppsala, Stockholm, Sweden

Abstract

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Introduction

The monoamine systems have been suggested to play a role for the biological background of ADHD symptoms. Thus, polymorphisms in e.g. the serotonin transporter (5HTT) gene have been associated with ADHD like phenotypes.

Furthermore, platelet MAOB activity has frequently been linked to impulsiveness-related traits.

Objective

Biological markers and candidate genes for psychiatric problems are often studied separately. We study ADHD symptoms with regard to the combination of platelet MAOB activity and 5HTT genotype.

Aim

To test the hypothesis that associations between ADHD like behavior problems and 5HTT-LPR polymorphism, would be more robust if calculations were done in combination with platelet MAOB enzyme activity.

Methods

The study group consisted of 156 adolescent twin pairs, i.e. 312 individuals. ADHD symptoms were scored with a structured clinical interview of both the twin and a parent using Kiddie Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL).

Results

Presence of a short 5HTT-LPR allele, in combination with high levels of platelet MAOB enzyme activity was associated with higher scores of ADHD like problems and disruptive behavior in boys. No such associations were found in girls.

Conclusion

This examination of ADHD scores in a non-clinical sample suggests that the effects of the 5HTT-LPR are moderated by platelet MAOB activity.

Type
Research Article
Copyright
Copyright © European Psychiatric Association2011
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