
PP94. THE SEROTONIN TRANSPORTER GENE: ANALYSIS OF HAPLOTYPES IN SUBSTANCE ABUSE G. FASKHUTDINOVA, E. Juriev, D. Gaysina, A. Zainullina, E. Khusnutdinova
Institute of Biochemistry and Genetics, Ufa Scientific Center, Russian Academy of Sciences, Ufa, Russian Federation
e-mail: faskhutdinova83@mail.ru
*Corresponding Author: page: 89
|
Abstract
The serotonin transporter (5-HTT) plays a critical role in regulating serotonergic neurotransmission. There is a substantial literature base that implicates serotonergic neurotransmission in alcohol and drug dependence, and therefore candidate genes for substance abuse include the gene encoding the serotonin transporter protein (encoded by SLC6A4). Two different polymorphisms (Stin2 VNTR and 5-HTTLPR) were examined using PCR method. The hypothesis that SLC6A4 gene polymorphisms may be associated with substance abuse was explored in Russian men with alcoholism (n=99), drug addiction (n=61) and in control group (n=132). Maximum likelihood analysis of haplotype distribution was performed by EH&2LD program. The presence of linkage disequilibrium between the two polymorphisms was demonstrated in men with alcoholism (χ2=16.92,p=0.0002), men with drug addiction (χ2=17.65,p=0.0001) and in controls (χ2=6.61,p=0.037). Our results of haplotype analysis didn't reveal any significant differences in global haplotypes distribution between groups of substance abusers and controls. Further analysis showed overrepresentation of the L10 haplotype among alcoholics compared to controls (χ2=5.62,p=0.018,OR=1.79,95%CI=1.1-2.9). The S12 haplotype had lower frequency in alcoholics compared to that in controls (χ2=4.41,p=0.036,OR=0.66,95%CI=0.43-0.97). Our findings confirm the association of SLC6A4 gene with alcohol dependence, but not with drug abuse in our sample.
|
|
|
|



 |
Number 27 VOL. 27 (2), 2024 |
Number 27 VOL. 27 (1), 2024 |
Number 26 Number 26 VOL. 26(2), 2023 All in one |
Number 26 VOL. 26(2), 2023 |
Number 26 VOL. 26, 2023 Supplement |
Number 26 VOL. 26(1), 2023 |
Number 25 VOL. 25(2), 2022 |
Number 25 VOL. 25 (1), 2022 |
Number 24 VOL. 24(2), 2021 |
Number 24 VOL. 24(1), 2021 |
Number 23 VOL. 23(2), 2020 |
Number 22 VOL. 22(2), 2019 |
Number 22 VOL. 22(1), 2019 |
Number 22 VOL. 22, 2019 Supplement |
Number 21 VOL. 21(2), 2018 |
Number 21 VOL. 21 (1), 2018 |
Number 21 VOL. 21, 2018 Supplement |
Number 20 VOL. 20 (2), 2017 |
Number 20 VOL. 20 (1), 2017 |
Number 19 VOL. 19 (2), 2016 |
Number 19 VOL. 19 (1), 2016 |
Number 18 VOL. 18 (2), 2015 |
Number 18 VOL. 18 (1), 2015 |
Number 17 VOL. 17 (2), 2014 |
Number 17 VOL. 17 (1), 2014 |
Number 16 VOL. 16 (2), 2013 |
Number 16 VOL. 16 (1), 2013 |
Number 15 VOL. 15 (2), 2012 |
Number 15 VOL. 15, 2012 Supplement |
Number 15 Vol. 15 (1), 2012 |
Number 14 14 - Vol. 14 (2), 2011 |
Number 14 The 9th Balkan Congress of Medical Genetics |
Number 14 14 - Vol. 14 (1), 2011 |
Number 13 Vol. 13 (2), 2010 |
Number 13 Vol.13 (1), 2010 |
Number 12 Vol.12 (2), 2009 |
Number 12 Vol.12 (1), 2009 |
Number 11 Vol.11 (2),2008 |
Number 11 Vol.11 (1),2008 |
Number 10 Vol.10 (2), 2007 |
Number 10 10 (1),2007 |
Number 9 1&2, 2006 |
Number 9 3&4, 2006 |
Number 8 1&2, 2005 |
Number 8 3&4, 2004 |
Number 7 1&2, 2004 |
Number 6 3&4, 2003 |
Number 6 1&2, 2003 |
Number 5 3&4, 2002 |
Number 5 1&2, 2002 |
Number 4 Vol.3 (4), 2000 |
Number 4 Vol.2 (4), 1999 |
Number 4 Vol.1 (4), 1998 |
Number 4 3&4, 2001 |
Number 4 1&2, 2001 |
Number 3 Vol.3 (3), 2000 |
Number 3 Vol.2 (3), 1999 |
Number 3 Vol.1 (3), 1998 |
Number 2 Vol.3(2), 2000 |
Number 2 Vol.1 (2), 1998 |
Number 2 Vol.2 (2), 1999 |
Number 1 Vol.3 (1), 2000 |
Number 1 Vol.2 (1), 1999 |
Number 1 Vol.1 (1), 1998 |
|
|