Association study of nicotinic-receptor variants and major depressive disorder

被引:27
作者
Lai, IC
Hong, CJ
Tsai, SJ
机构
[1] Vet Gen Hosp Taipei, Dept Psychiat, Taipei 11217, Taiwan
[2] Natl Yang Ming Univ, Sch Med, Div Psychiat, Taipei 112, Taiwan
关键词
association study; polymorphism; nicotinic receptor; major depressive disorder;
D O I
10.1016/S0165-0327(00)00292-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Depressive patients are more likely to smoke than the general population and nicotine was found to reduce the incidence and severity of depressive symptoms in many studies. These findings suggest that nicotinic acetylcholine receptors (nAChRs) may be implicated in major depressive disorder. We tested the hypothesis that the allelic variant, 2 bp deletion, of the partially duplicated alpha7 nAChR gene confers susceptibility to major depressive disorder. Methods: We genotyped alpha7 nAChR in 72 patients with major depressive disorder and 103 normal controls. Results: The distribution of the partially duplicated alpha7 nAChR genotypes (P = 0.027) and alleles (P = 0.037) suggests a modest difference between depressive patients and controls. Limitations: The -2 bp allele is thought to be present only in the duplicated exon 6, and the impact of the partially duplicated alpha7 nAChR and its -2 bp variant remain to be determined. Conclusions: The -2 bp allele of partially duplicated alpha nAChR may have an influence on the risk for development of major depressive disorder. The levels of significance achieved are modest and the findings must be replicated in other studies. (C) 2001 Elsevier Science BY All rights reserved.
引用
收藏
页码:79 / 82
页数:4
相关论文
共 11 条
[1]   Genomic variation and gene conversion in spinal muscular atrophy: Implications for disease process and clinical phenotype [J].
Campbell, L ;
Potter, A ;
Ignatius, J ;
Dubowitz, V ;
Davies, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (01) :40-50
[2]   A NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTOR SUBUNIT (ALPHA-7) IS DEVELOPMENTALLY REGULATED AND FORMS A HOMOOLIGOMERIC CHANNEL BLOCKED BY ALPHA-BTX [J].
COUTURIER, S ;
BERTRAND, D ;
MATTER, JM ;
HERNANDEZ, MC ;
BERTRAND, S ;
MILLAR, N ;
VALERA, S ;
BARKAS, T ;
BALLIVET, M .
NEURON, 1990, 5 (06) :847-856
[3]  
Covey LS, 1997, AM J PSYCHIAT, V154, P263
[4]   Antidepressants noncompetitively inhibit nicotinic acetylcholine receptor function [J].
Fryer, JD ;
Lukas, RJ .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (03) :1117-1124
[5]   Genomic organization and partial duplication of the human α7 neuronal nicotinic acetylcholine receptor gene (CHRNA7) [J].
Gault, J ;
Robinson, M ;
Berger, R ;
Drebing, C ;
Logel, J ;
Hopkins, J ;
Moore, T ;
Jacobs, S ;
Meriwether, J ;
Choi, MJ ;
Kim, EJ ;
Walton, K ;
Buiting, K ;
Davis, A ;
Breese, C ;
Freedman, R ;
Leonard, S .
GENOMICS, 1998, 52 (02) :173-185
[6]  
GLASSMAN AH, 1993, AM J PSYCHIAT, V150, P546
[7]  
KENDLER KS, 1993, ARCH GEN PSYCHIAT, V50, P36
[8]   ORGANIZATION OF THE HUMAN TRANSFERRIN GENE - DIRECT EVIDENCE THAT IT ORIGINATED BY GENE DUPLICATION [J].
PARK, I ;
SCHAEFFER, E ;
SIDOLI, A ;
BARALLE, FE ;
COHEN, GN ;
ZAKIN, MM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (10) :3149-3153
[9]   Development of depression during placebo-controlled trials of bupropion for smoking cessation: Case reports [J].
Patten, CA ;
Rummans, TA ;
Croghan, IT ;
Hurt, RD ;
Hays, JT .
JOURNAL OF CLINICAL PSYCHIATRY, 1999, 60 (07) :436-441
[10]   INHIBITION OF NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTORS BY IMIPRAMINE AND DESIPRAMINE [J].
RANA, B ;
MCMORN, SO ;
REEVE, HL ;
WYATT, CN ;
VAUGHAN, PFT ;
PEERS, C .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 250 (02) :247-251