Association of the SAT1 In/Del Polymorphism With Suicide Completion

作者：Fiori Laura M; Turecki Gustavo^*

来源：American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 2010, 153B(3): 825-829.

DOI：10.1002/ajmg.b.31040

• polyamines
• SAT1
• insertion/deletion polymorphism
• suicide
• depressive disorders

Several studies have observed decreased expression of spermidine/spermine N1-acetyltransferase (SAT1) in the brains of suicide completers, and we previously identified a single-nucleotide polymorphism in the promoter region of SAT1 which was associated with suicide completion and SAT1 expression in the brain. We recently characterized the haplotype structure of the SAT1 promoter region and identified an insertion/deletion (in/del) of 15 adenine residues. This variant appears to be a predictor of SAT1 expression, and we were thus interested in determining if the lower expressing deletion allele was found more frequently among suicide completers. To this end, we genotyped the in/del in a sample of 771 French-Canadian males, comprising 326 suicide completers and 445 non-suicide controls. We found no significant difference in the frequencies of the two alleles between suicide completers and controls in the entire sample. However, we observed a significantly higher frequency of the deletion in the depressed suicide completers compared to the depressed non-suicides. These results add support for a role of SAT1 in conferring a risk for suicide completion, in particular in the context of depressive disorders.

• 出版日期2010-4