Prediction of level of serotonin 2A receptor binding by serotonin receptor 2A genetic variation in postmortem brain samples from subjects who did or did not commit suicide
- PMID: 10484964
- DOI: 10.1176/ajp.156.9.1456
Prediction of level of serotonin 2A receptor binding by serotonin receptor 2A genetic variation in postmortem brain samples from subjects who did or did not commit suicide
Abstract
Objective: Postmortem studies have indicated that suicide victims have greater serotonin receptor 2A (5-HTR2A) binding in prefrontal brain regions. However, there remains some controversy regarding the biological specificity of these findings. The authors hypothesized that the variance observed in brain 5-HTR2A binding is genetically mediated, at least in part.
Method: Postmortem data from 56 subjects who had committed suicide and 126 normal comparison subjects were studied; brain tissue was available from 11 subjects who committed suicide and 11 comparison subjects. Homogenate binding assays were carried out with [3H]ketanserin. Variation at the 5-HTR2A gene (HTR2A) was investigated by means of two polymorphisms: T102C and A-1438G.
Results: 5-HTR2A binding was greater in the prefrontal cortex of the subjects who committed suicide. In addition, the findings suggest that HTR2A variation significantly affects 5-HTR2A binding. However, no interaction between suicidal behavior and this locus was observed.
Conclusions: These results confirm previous reports of greater 5-HTR2A binding in subjects who committed suicide; they also provide preliminary evidence suggesting that the number of 5-HTR2A receptors is genetically mediated.
Comment in
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Serotonin 2A receptor polymorphisms and [(3)H]Ketanserin binding.Am J Psychiatry. 2000 Oct;157(10):1710-1. doi: 10.1176/appi.ajp.157.10.1710. Am J Psychiatry. 2000. PMID: 11007744 No abstract available.
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Levels of serotonin receptor 2A higher in suicide victims?Am J Psychiatry. 2001 Jan;158(1):147-8. doi: 10.1176/appi.ajp.158.1.147-a. Am J Psychiatry. 2001. PMID: 11136659 No abstract available.
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