Association study of the serotonin transporter promoter polymorphism and symptomatology and antidepressant response in major depressive disorders

被引:190
作者
Yu, YWY
Tsai, SJ
Chen, TJ
Lin, CH
Hong, CJ
机构
[1] Vet Gen Hosp, Dept Psychiat, Taipei 11217, Taiwan
[2] Kai Suan Psychiat Hosp, Kaohsiung, Taiwan
[3] Yu Psychiat Clin, Kaohsiung, Taiwan
[4] Natl Yang Ming Univ, Sch Med, Div Psychiat, Taipei 112, Taiwan
关键词
major depressive disorders; polymorphism; selective serotonin reuptake inhibitors; serotonin transporter; treatment response;
D O I
10.1038/sj.mp.4001141
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
The serotonin transporter (5-HTT) is the site of primary action for the selective serotonin reuptake inhibitors (SSRIs). Previous Western reports have demonstrated that the I allele of the 5-HTT gene-linked polymorphic-region (5-HTTLPR) polymorphism is associated with better SSRI antidepressive effects than the s allele, however, another study of a Korean population has produced a contrasting finding. The present study tested the hypothesis that the 5-HTTLPR genetic polymorphism is associated with SSRI antidepressant response by evaluating total and cluster depressive symptoms for 121 Chinese patients diagnosed with major depression. Analysis of the results reveals that patients with the I/I genotype had a significantly better response to SSRI (fluoxetine) when compared with s allele carriers, as evaluated on the basis of total (P = 0.013), core (P = 0.011), and psychic-anxiety (P = 0.005) and somatic-anxiety (P = 0.002) Hamilton Depression Rating Scale-score percentage change. Our findings confirm reports that the I allele is associated with better SSRI response.
引用
收藏
页码:1115 / 1119
页数:5
相关论文
共 24 条
[1]   Possible influence of the insertion/deletion polymorphism in the angiotensin I-converting enzyme gene on therapeutic outcome in affective disorders [J].
Baghai, TC ;
Schüle, C ;
Zwanzger, P ;
Minov, C ;
Schwarz, MJ ;
de Jonge, S ;
Rupprecht, R ;
Bondy, B .
MOLECULAR PSYCHIATRY, 2001, 6 (03) :258-259
[2]  
Burke WJ, 1996, PSYCHOPHARMACOL BULL, V32, P27
[3]   Assessment of serotonergic function in major depression using d-fenfluramine:: Relation to clinical variables and antidepressant response [J].
Cleare, AJ ;
Murray, RM ;
O'Keane, V .
BIOLOGICAL PSYCHIATRY, 1998, 44 (07) :555-561
[4]   Altered expression and functions of serotonin 5-HT1A and 5-HT1B receptors in knock-out mice lacking the 5-HT transporter [J].
Fabre, V ;
Beaufour, C ;
Evrard, A ;
Rioux, A ;
Hanoun, N ;
Lesch, KP ;
Murphy, DL ;
Lanfumey, L ;
Hamon, M ;
Martres, MP .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (07) :2299-2310
[5]  
Fava M, 2000, J CLIN PSYCHIAT, V61, P10
[6]   Dissecting the role of the serotonin system in neuropsychiatric disorders using knockout mice [J].
Gingrich, JA ;
Hen, R .
PSYCHOPHARMACOLOGY, 2001, 155 (01) :1-10
[7]  
Gobbi G, 2001, J PHARMACOL EXP THER, V296, P987
[8]  
Hamilton M., 1967, British Journal of Social and Clinical Psychology, V6, P278
[9]  
Heils A, 1996, J NEUROCHEM, V66, P2621
[10]   Serotonin transporter gene polymorphism and antidepressant response [J].
Kim, DK ;
Lim, SW ;
Lee, S ;
Sohn, SE ;
Kim, S ;
Hahn, CG ;
Carroll, BJ .
NEUROREPORT, 2000, 11 (01) :215-219