Abstract
Objective: Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder. The genetic cause of ADHD is still unclear, but the dopaminergic, serotonergic, and noradrenergic pathways have shown a strong association. In particular, monoamine oxidase A (MAOA) plays an important role in the catabolism of these neurotransmitters, suggesting that the MAOA gene is associated with ADHD. Therefore, we evaluated the relationship between the MAOA gene polymorphisms (uVNTR and rs6323) and ADHD. Materials and methods: We collected a total of 472 Korean children (150 ADHD cases and 322 controls) using the Korean version of the Dupaul Attention Deficit Hyperactivity Disorder Rating Scales (K-ARS). Genotyping was performed by PCR and PCR-RFLP. The Behavior Assessment System for Children Second Edition (BASC-2) was used to evaluate the problem behaviors within ADHD children. Results: We observed significant associations between the rs6323 and ADHD in girls (p < 0.05) and the TT genotype was observed as a protective factor against ADHD in the recessive model (OR 0.31, 95% CI 0.100–0.950, p = 0.022). The 3.5R-G haplotype showed a significant association in ADHD boys (p = 0.043). The analysis of subtype also revealed that the 4.5R allele of uVNTR was a risk factor for the development of ADHD in the combined symptom among girls (OR 1.87, 95% CI 1.014–3.453, p = 0.031). In the BASC-2 analysis, the MAOA uVNTR polymorphism was associated with activities of daily living in ADHD boys (p = 0.017). Conclusion: These results suggest the importance of the MAOA gene polymorphisms in the development of ADHD in Korean children. A larger sample set and functional studies are required to further elucidate of our findings.
Highlights
Attention Deficit Hyperactivity Disorder (ADHD) is one of the most common neurodevelopmental disorders with a prevalence of 8.5% among the Korean children [1]
monoamine oxidase A (MAOA) gene polymorphisms were shown to be associated with the development of ADHD and behavioral traits
We observed that the rs6323 TT genotype was a protective factor against ADHD in Korean children
Summary
Attention Deficit Hyperactivity Disorder (ADHD) is one of the most common neurodevelopmental disorders with a prevalence of 8.5% among the Korean children [1] It is characterized by clinical symptoms of inattentive or hyperactive and impulsive behavior [2]. The genetic etiology of ADHD is still unclear, and many studies have reported that the genes related to the dopaminergic, serotonergic, and noradrenergic pathways are significantly associated with ADHD [4,5,6,7]. Among these genes, the DRD4 and DAT1 gene VNTR polymorphisms of the Medicina 2018, 54, 32; doi:10.3390/medicina54030032 www.mdpi.com/journal/medicina.
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