Tryptophan hydroxylase 2 gene and alcohol use among college students

被引:21
作者
Gacek, Paul [1 ]
Conner, Tamlin S. [2 ]
Tennen, Howard [1 ,3 ]
Kranzler, Henry R. [3 ]
Covault, Jonathan [3 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Commun Med & Hlth Care, Publ Hlth Program, Farmington, CT 06030 USA
[2] Univ Otage, Dept Psychol, Dunedin, New Zealand
[3] Univ Connecticut, Ctr Hlth, Dept Psychiat, Alcohol Res Ctr, Farmington, CT 06030 USA
关键词
alcohol; college drinking; gene-environment interaction; heavy drinking; tryptophan hydroxylase; TPH2;
D O I
10.1111/j.1369-1600.2008.00118.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genes that regulate serotonin activity are regarded as promising predictors of heavy alcohol use. Tryptophan hydroxylase (TPH2) plays an important role in serotonergic neurotransmission by serving as the rate-limiting enzyme for serotonin biosynthesis in the midbrain and serotonergic neurons. Despite the link between TPH2 and serotonergic function, TPH2's role in the pathogenesis of alcohol-use disorders remains unclear. The goal of this study was to examine whether a variation in the TPH2 gene is associated with risky alcohol consumption. Specifically, this study examined whether the TPH2 G-703T polymorphism predicted alcohol consumption among college students. In two successive years, 351 undergraduates were asked to record their alcohol use each day for 30 days using an Internet-based electronic diary. Participants' DNA was collected and polymerase chain reaction genotyping was performed. Results show that alcohol consumption was not associated with the TPH2 G-703T polymorphism alone, or the interaction of TPH2 with two other candidate polymorphisms (TPH1 C218A and the SLC6A4 tri-allelic 5-HTTLPR), or negative life events. In conclusion, this study supports recent null findings relating TPH2 to drinking outcomes. It also extends these findings by showing null interactions with the TPH1 C218A polymorphism, the SLC6A4 tri-allelic 5-HTTLPR polymorphism and environmental stressors in predicting sub-clinical alcohol use among Caucasian American young adults.
引用
收藏
页码:440 / 448
页数:9
相关论文
共 40 条
[1]  
Aiken L. S., 1991, Multiple Regression: Testing and Interpreting Interactions
[2]   A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity [J].
Brown, SM ;
Peet, E ;
Manuck, SB ;
Williamson, DE ;
Dahl, RE ;
Ferrell, RE ;
Hariri, AR .
MOLECULAR PSYCHIATRY, 2005, 10 (09) :884-888
[3]   Amygdala responsiveness is modulated by tryptophan hydroxylase-2 gene variation [J].
Canli, T ;
Congdon, E ;
Gutknecht, L ;
Constable, RT ;
Lesch, KP .
JOURNAL OF NEURAL TRANSMISSION, 2005, 112 (11) :1479-1485
[4]   Opinion - Gene-environment interactions in psychiatry: joining forces with neuroscience [J].
Caspi, Avshalom ;
Moffitt, Terrie E. .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (07) :583-590
[5]   Tryptophan hydroxylase polymorphism is associated with age of onset of alcoholism related behaviors [J].
Chung, IW ;
Kim, H ;
Sribney, W ;
Hong, JB ;
Lee, CH ;
Lee, KY ;
Nan, HM ;
Kim, YS ;
Manowitz, P .
ALCOHOL, 2005, 36 (01) :1-3
[6]   The life events scale for students: Validation for use with British samples [J].
Clements, K ;
Turpin, G .
PERSONALITY AND INDIVIDUAL DIFFERENCES, 1996, 20 (06) :747-751
[7]  
COHEN EGD, 1971, STAT MECH TURN DECAD
[8]   Maternal serotonin is crucial for murine embryonic development [J].
Cote, Francine ;
Fligny, Cecile ;
Bayard, Elisa ;
Launay, Jean-Marie ;
Gershon, Michael D. ;
Mallett, Jacques ;
Vodjdani, Guilan .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (01) :329-334
[9]   Interactive effects of the serotonin transporter 5-HTTLPR polymorphism and stressful life events on college student drinking and drug use [J].
Covault, Jonathan ;
Tennen, Howard ;
Armeli, Stephen ;
Conner, Tamlin S. ;
Herman, Aryeh I. ;
Cillessen, Antonius H. N. ;
Kranzler, Henry R. .
BIOLOGICAL PSYCHIATRY, 2007, 61 (05) :609-616
[10]   The HTR1B 861G>C receptor polymorphism among patients suffering from alcoholism, major depression, anxiety disorders and narcolepsy [J].
Fehr, C ;
Grintschuk, N ;
Szegedi, A ;
Anghelescu, I ;
Klawe, C ;
Singer, P ;
Hiemke, C ;
Dahmen, N .
PSYCHIATRY RESEARCH, 2000, 97 (01) :1-10