Lack of an association between 5‐HT1A receptor gene structural polymorphisms and suicide victims |
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Authors: | Naoki Nishiguchi Hisae Ono Akiyoshi Nishimura Hideyuki Nushida Yasuhiro Ueno Kiyoshi Maeda |
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Affiliation: | 1. Division of Psychiatry and Neurology, Department of Environmental Health and Safety Faculty of Medical Sciences, Kobe University Graduate School of Medicine, Kobe, Japan;2. Department of Legal Medicine, Yokohama City University School of Medicine, Yokohama, Japan;3. Division of Legal Medicine, Department of Environment Health and Safety, Faculty of Medical Sciences, Kobe University Graduate School of Medicine, Kobe, Japan |
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Abstract: | A serotonergic dysfunction in the brain has been reported to be involved in suicidal behavior independently of the presence of a specific psychiatric disorder. Serotonin 1A (5‐HT1A) receptors are known to be located on serotonergic nerve terminals and to be involved in the presynaptic regulation of serotonin release. Genetic factors partly explain the risks for suicide, and a suicide completion group is thought to be more uniform than a suicide attempt group. To explore the hypothesis that the 5‐HT1A receptor‐induced serotonergic dysfunction is implicated genetically in suicide, we focused on the structural polymorphisms, Pro16Leu and Gly272Asp, of the 5‐HT1A receptor gene, and examined the association between suicide victims who completed suicide and these two polymorphisms. In both polymorphisms, we found no significant difference in genotype distribution or allele frequencies between suicide victims and controls. These findings suggest that neither of these two polymorphisms is associated with suicide victims and it is unlikely that the 5‐HT1A receptor gene is implicated in the susceptibility to suicide. © 2002 Wiley‐Liss, Inc. |
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Keywords: | 5‐HT1A receptor genetics suicide victims association study structural polymorphisms |
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