| Literature DB >> 9654330 |
T Türker1, R Sodmann, U Goebel, S Jatzke, M Knapp, K P Lesch, R Schuster, H Schütz, G Weiler, G Stöber.
Abstract
Central serotonergic neurotransmission has been implicated in the aetiology of ethanol tolerance and dependence. Cellular expression of the serotonin transporter and serotonin reuptake is modulated via a polymorphic, repetitive element in the 5'-flanking regulatory region of the serotonin transporter gene (5-HTTLPR). We report the association of the low-activity, short variant of the 5-HTTLPR with high ethanol tolerance among young adults in a case-control association study (n = 713). The low-activity 5-HTTLPR showed a significantly increased allele frequency (chi2 = 7.30; df = 2; P = 0.007) and genotype frequency among young adults (< or =26 years) with high ethanol tolerance homozygous for the short allele (chi2 = 7.58; df = 1; P = 0.02). The estimated odds ratio for the homozygous short variant compared to the homozygous long variant was 2.82 (95% CI 1.30-6.11). This indicates that the low-activity 5-HTTLPR may be involved in the neuronal mechanisms responsible for ethanol tolerance and dependence.Entities:
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Year: 1998 PMID: 9654330 DOI: 10.1016/s0304-3940(98)00347-4
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046