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Serotonin transporter gene polymorphism associated with short-term treatment response to venlafaxine

Authors
 Sang-Hyuk Lee  ;  Tae Kyou Choi  ;  Eun Lee  ;  Jeong-Ho Seok  ;  Sung Hee Lee  ;  Hong Shick Lee  ;  Se Joo Kim 
Citation
 NEUROPSYCHOBIOLOGY, Vol.62(3) : 198-206, 2010 
Journal Title
NEUROPSYCHOBIOLOGY
ISSN
 0302-282X 
Issue Date
2010
MeSH
Adult ; Alleles ; Asian Continental Ancestry Group/genetics ; Cyclohexanols/administration & dosage* ; Delayed-Action Preparations/administration & dosage ; Depressive Disorder, Major/drug therapy* ; Depressive Disorder, Major/genetics* ; Drug Administration Schedule ; Female ; Genotype ; Humans ; Male ; Middle Aged ; Polymorphism, Genetic ; Psychiatric Status Rating Scales ; Serotonin Plasma Membrane Transport Proteins/genetics* ; Serotonin Uptake Inhibitors/administration & dosage* ; Venlafaxine Hydrochloride
Keywords
5-HTTLPR polymorphism ; Treatment response ; Venlafaxine ; Genetics
Abstract
BACKGROUND: Polymorphisms of serotonin transporter, especially serotonin transporter linked promoter region (5- HTTLPR) and serotonin transporter intron 2 variable number tandem repeat (5-HTTVNTR), have been suggested to be associated with treatment response to selective serotonin reuptake inhibitors. However, there have been only few reports of the association between 5-HTTLPR or 5-HTTVNTR and treatment response to venlafaxine.

METHODS: 84 Korean major depressive disorder patients were included in this study. They were administered 75 mg of venlafaxine XR (extended release) for 1 week and then took 150 mg for the next 3 weeks. All patients were evaluated at baseline and week 4 by the Hamilton Depression Rating Scale (HAM-D), Montgomery-Asberg Depression Rating Scale (MADRS), Beck Depression Inventory (BDI), Hamilton Anxiety Rating Scale (HAM-A), and Beck Anxiety Inventory (BAI).

RESULTS: (1) Treatment response of depressive symptoms (BDI, HAM-D, MADRS) to venlafaxine at week 4 was associated with the non-s/s (l/l and l/s) genotype of 5-HTTLPR; (2) in repeated measures ANOVA, the BDI, MADRS and HAM-A scores decreased more significantly in patients with the non-s/s genotype than in those with the s/s genotype, and (3) multiple regression analyses suggested that the 5-HTTLPR polymorphism is a predictive factor for short-term treatment response to venlafaxine. However, 5-HTTVNTR showed no significant association with treatment response to venlafaxine. Both 5-HTTLPR and 5-HTTVNTR were not associated with side effects of venlafaxine.

CONCLUSION: The 5-HTTLPR non-s/s genotype can be associated with venlafaxine treatment responses. However, further large-scale studies are warranted to confirm this finding.
Files in This Item:
T201002337.pdf Download
DOI
10.1159/000319362
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Psychiatry (정신과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Se Joo(김세주) ORCID logo https://orcid.org/0000-0002-5438-8210
Seok, Jeong Ho(석정호) ORCID logo https://orcid.org/0000-0002-9402-7591
Lee, Sung Hee(이성희)
Lee, Eun(이은) ORCID logo https://orcid.org/0000-0002-7462-0144
Lee, Hong Shick(이홍식)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/101539
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