~ W e have tested the hypothesis that DNA markers in the MAOA gene show allelic association with bipolar affective disorder. Eighty-four unrelated Caucasian patients with DSM 111-R bipolar disorder and 84 Caucasian controls were typed for three markers in MAOA a dinucleotide repeat in intron 2, a VN
No evidence of an association between a functional monoamine oxidase a gene polymorphism and completed suicides
β Scribed by Ono, Hisae ;Shirakawa, Osamu ;Nishiguchi, Naoki ;Nishimura, Akiyoshi ;Nushida, Hideyuki ;Ueno, Yasuhiro ;Maeda, Kiyoshi
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 67 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Monoamine oxidase A (MAOA) has been implicated in the control of aggression and/or impulsivity in humans and been involved in suicide. This gene has a functional polymorphism in which there is a variable number tandem repeat (VNTR) in the upstream region (MAOAβuVNTR). We hypothesized that MAOA dysfunction due to this polymorphism was associated with suicide genetically through the disinhibition of aggression and/or impulsivity. We performed an association study between completed suicides and the MAOAβuVNTR polymorphism. No significant difference in genotype distribution or allele frequencies was found between completed suicides and comparison groups either in males or females. These results show no evidence of an association between the MAOAβuVNTR polymorphism and completed suicides and suggest that MAOA is not involved in the susceptibility to suicide. Β© 2002 WileyβLiss, Inc.
π SIMILAR VOLUMES
Serotonergic systems have been reported to mediate the control of aggression and/or impulsivity in humans and to be involved in suicidal behavior. Neurochemical studies showing serotonergic dysfunction in suicide appear to support the functional alteration of serotonergic systems due to gene polymor
## Monoamine oxidase B (MAO -B ) is an enzyme that has relevance for Parkinson disease (PD) because of its roles in catabolizing dopamine and potentially activating exogenous neurotoxicants. A polymorphism of the gene encoding MAO-B has been identified as a single base change (A or G) in intron