5-HTTLPR polymorphism of the serotonin transporter gene predicts non-remission in major depression patients treated with citalopram in a 12-weeks follow up study

被引:144
作者
Arias, B
Catalán, R
Gastó, C
Gutiérrez, B
Fañanás, L
机构
[1] Univ Barcelona, Fac Biol, Dept Biol Anim, Unitat Antropol, E-08028 Barcelona, Spain
[2] Univ Barcelona, Fundacio Clin Recerca Biomed, Barcelona, Spain
[3] Hosp Clin Barcelona, Ctr Salut Mental Esquerre Eixample, Barcelona, Spain
关键词
D O I
10.1097/01.jcp.0000095350.32154.73
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the context of a long term follow-up study, we analysed the possible implication of the 5-HTTLPR polymorphism at the serotonin transporter gene in clinical response and remission of major depressive patients treated with citalopram. The sample consisted of 131 patients, all of Spanish origin, diagnosed according to DSM-IV criteria. A 21-item Hamilton Depression Rating Scale (HDRS) was used to evaluate severity of the symptoms during the follow-up and to determine clinical response and remission condition of the patients at 4th and 12th week, respectively. Our results showed that S/S genotype of the 5-HTTLPR polymorphism was associated with the non-Remission condition at 12th week (chi(2) = 8.7, P = 0.013). Moreover, homozygous for the allele S presented three times more risk for non reaching remission of depressive episode after citalopram treatment than patients with any other 5-HTTLPR genotype combination (chi(2) : 7.29, P = 0.006; OR = 3.23 [95% CI: 1.24-8.5]). In conclusion, our results show that genetic variation of serotonin transporter is involved in clinical remission of major depressive episodes after twelve weeks of citalopram treatment.
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页码:563 / 567
页数:5
相关论文
共 29 条
[1]  
Allison DB, 1997, AM J HUM GENET, V60, P676
[2]   Pharmacogenetic prediction of clozapine response [J].
Arranz, MJ ;
Munro, J ;
Birkett, J ;
Bolonna, A ;
Mancama, D ;
Sodhi, M ;
Lesch, KP ;
Meyer, JFW ;
Sham, P ;
Collier, DA ;
Murray, RM ;
Kerwin, RW .
LANCET, 2000, 355 (9215) :1615-1616
[3]  
Baum C, 1996, GENE THER, V3, P1
[4]  
BAUMAN HE, 1995, ADV MEAT RES, V10, P1
[5]   A double-blind, placebo-controlled study of citalopram with and without lithium in the treatment of therapy-resistant depressive patients: A clinical, pharmacokinetic, and pharmacogenetic investigation [J].
Baumann, P ;
Nil, R ;
Souche, A ;
Montaldi, S ;
Baettig, D ;
Lambert, S ;
Uehlinger, C ;
Kasas, A ;
Amey, M ;
JonzierPerey, M .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1996, 16 (04) :307-314
[6]   Depressive illness [J].
Doris, A ;
Ebmeier, K ;
Shajahan, P .
LANCET, 1999, 354 (9187) :1369-1375
[7]  
ENSERICK M, 1999, SCIENCE, V184, P196
[8]   CONCEPTUALIZATION AND RATIONALE FOR CONSENSUS DEFINITIONS OF TERMS IN MAJOR DEPRESSIVE DISORDER - REMISSION, RECOVERY, RELAPSE, AND RECURRENCE [J].
FRANK, E ;
PRIEN, RF ;
JARRETT, RB ;
KELLER, MB ;
KUPFER, DJ ;
LAVORI, PW ;
RUSH, AJ ;
WEISSMAN, MM .
ARCHIVES OF GENERAL PSYCHIATRY, 1991, 48 (09) :851-855
[9]   Delayed pharmacological effects of antidepressants [J].
Frazer, A ;
Benmansour, S .
MOLECULAR PSYCHIATRY, 2002, 7 (Suppl 1) :S23-S28
[10]   How fast are antidepressants? [J].
Gelenberg, AJ ;
Chesen, CL .
JOURNAL OF CLINICAL PSYCHIATRY, 2000, 61 (10) :712-721