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MAOA variants differ in oscillatory EEG & ECG activities in response to aggression-inducing stimuli
- Department of Brain Sciences
- Laboratory of Chemical Senses
- 1. Journal Articles
- Department of New Biology
- Biointerface Structure and Skin Lab
- 1. Journal Articles
- Department of Brain Sciences
- Laboratory of Environmental Biotechnology
- 1. Journal Articles
- Department of New Biology
- Lab of Integrative Animal Ecology
- 1. Journal Articles
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- Title
- MAOA variants differ in oscillatory EEG & ECG activities in response to aggression-inducing stimuli
- Issued Date
- 2019-02
- Citation
- Im, Seung Yeong. (2019-02). MAOA variants differ in oscillatory EEG & ECG activities in response to aggression-inducing stimuli. Scientific Reports, 9(1). doi: 10.1038/s41598-019-39103-7
- Type
- Article
- Keywords
- MONOAMINE-OXIDASE-A ; HUMAN SEROTONIN TRANSPORTER ; HEART-RATE REACTIVITY ; ANTISOCIAL-BEHAVIOR ; FUNCTIONAL POLYMORPHISM ; CHILDHOOD MALTREATMENT ; GENE PROMOTER ; POINT MUTATION ; BRAIN ACTIVITY ; GENOTYPE
- ISSN
- 2045-2322
- Abstract
-
Among the genetic variations in the monoamine oxidase A (MAOA) gene, upstream variable number tandem repeats (uVNTRs) of the promoter have been associated with individual differences in human physiology and aggressive behaviour. However, the evidence for a molecular or neural link between MAOA uVNTRs and aggression remains ambiguous. Additionally, the use of inconsistent promoter constructs in previous studies has added to the confusion. Therefore, it is necessary to demonstrate the genetic function of MAOA uVNTR and its effects on multiple aspects of aggression. Here, we identified three MAOA alleles in Koreans: the predominant 3.5R and 4.5R alleles, as well as the rare 2.5R allele. There was a minor difference in transcriptional efficiency between the 3.5R and 4.5R alleles, with the greatest value for the 2.5R allele, in contrast to existing research. Psychological indices of aggression did not differ among MAOA genotypes. However, our electroencephalogram and electrocardiogram results obtained under aggression-related stimulation revealed oscillatory changes as novel phenotypes that vary with the MAOA genotype. In particular, we observed prominent changes in frontal γ power and heart rate in 4.5R carriers of men. Our findings provide genetic insights into MAOA function and offer a neurobiological basis for various socio-emotional mechanisms in healthy individuals. © 2019, The Author(s).
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- Publisher
- Nature Publishing Group
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