Aggressiveness in Italian Children with ADHD: MAOA Gene Polymorphism Involvement

Author:

Neri Ludovico1,Marziani Beatrice2ORCID,Sebastiani Pierluigi3,Del Beato Tiziana3,Colanardi Alessia3,Legge Maria Pia1,Aureli Anna3ORCID

Affiliation:

1. Neurology and Psychiatry Unit for Children and Adolescents, San Salvatore Hospital, via L. Natali, 1, Coppito, 67100 L’Aquila, Italy

2. Emergency Medicine Department, Sant’Anna University Hospital, Via A. Moro, 8, Cona, 44124 Ferrara, Italy

3. CNR Institute of Translational Pharmacology, Via Carducci 32, 67100 L’Aquila, Italy

Abstract

ADHD is a neurodevelopmental disorder that children and adults can develop. A complex interplay of genetic and environmental factors may underlie interindividual variability in ADHD and potentially related aggressive behavior. Using high-resolution molecular biology techniques, we investigated the impact of some MAOA and SLC6A4 variations on ADHD and aggressive behavior in a group of 80 Italian children with ADHD and in 80 healthy controls. We found that homozygous genotypes of MAOA rs6323 and rs1137070 were associated with an increased risk of ADHD (p = 0.02 and p = 0.03, respectively), whereas the heterozygous genotypes (GT of rs6323 and CT of rs1137030) (p = 0.0002 and p = 0.0006) were strongly linked to a lower risk of developing this disorder. In patients with aggressive behavior, we highlighted only a weak negative association of both MAOA polymorphisms (heterozygous genotypes) with aggressiveness, suggesting that these genotypes may be protective towards specific changes in behavior (p = 0.05). Interestingly, an increase in the GG genotype of rs6323 (p = 0.01) and a decrease in GT genotype (p = 0.0005) was also found in patients without aggressive behavior compared to controls. Regarding 5HTT gene genotyping, no allele and genotype differences have been detected among patients and controls. Our work shows that defining a genetic profile of ADHD may help in the early detection of patients who are more vulnerable to ADHD and/or antisocial and aggressive behavior and to design precision-targeted therapies.

Funder

National Research Council

Publisher

MDPI AG

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