Dopamine Beta-Hydroxylase (DBH) gene and schizophrenia phenotypic variability: A genetic association study

被引:38
作者
Yamamoto, K
Cubells, JF
Gelernter, J
Benkelfat, C
Lalonde, P
Bloom, D
Lal, S
Labelle, A
Turecki, G
Rouleau, GA
Joober, R
机构
[1] Douglas Hosp, Res Ctr, Verdun, PQ H4H 1R3, Canada
[2] Tokai Univ, Sch Med, Dept Psychiat & Behav Sci, Kanagawa 2591193, Japan
[3] Yale Univ, Sch Med, Dept Psychiat, West Haven, CT 06516 USA
[4] VA Connecticut Hlth Care Syst, West Haven, CT 06516 USA
[5] McGill Univ, Dept Psychiat, Montreal, PQ H3A 1A1, Canada
[6] Univ Montreal, Montreal, PQ H1N 1C1, Canada
[7] LH Lafontaine Hosp, Montreal, PQ H1N 1C1, Canada
[8] Montreal Gen Hosp, Res Inst, Montreal, PQ H3G 1A4, Canada
[9] Royal Ottawa Hosp, Ottawa, ON K1Z 7K4, Canada
[10] Univ Ottawa, Ottawa, ON K1Z 7K4, Canada
来源
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS | 2003年 / 117B卷 / 01期
关键词
Dopamine Beta-Hydroxylase; schizophrenia; positive symptom; neuroleptic responsiveness; population stratification;
D O I
10.1002/ajmg.b.10011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recently, two polymorphisms (DBH5'-Ins/del and DBH 444 g/a) of the Dopamine Beta Hydroxylase (DBH) gene were isolated, and one haplotype (Del-a) was found to be associated with low DBH activity and cocaine-induced paranoia. The purpose of this study is to test for association between these two polymorphisms and schizophrenia or its phenotypic variability with respect to neuroleptic therapeutic response and symptom profile. Allelic and haplotype distributions of these two polymorphisms were compared between two groups of schizophrenic patients (excellent neuroleptic-responders; R, n=42 and non-responders; NR, n=64), and one group of healthy volunteers (n=120). The "Del" and "a" alleles were in positive linkage disequilibrium. No allelic or genotype differences in the distribution of these two polymorphisms were observed between patients and controls. However, The Del-a haplotype was significantly more common in NR patients, and the mean total BPRS score was significantly higher in the group of patients with the Del-a compared to those without the Del-a haplotype. These results suggest that the DBH gene is not a causative factor in schizophrenia but that it may be a modulator of psychotic symptoms, severity of the disorder and therapeutic response to neuroleptic drugs. (C)2003 Wiley-Liss, Inc.
引用
收藏
页码:33 / 38
页数:6
相关论文
共 34 条
[1]  
[Anonymous], ARCH GEN PSYCHIAT
[2]   REDUCED SERUM DOPAMINE-BETA-HYDROXYLASE ACTIVITY IN PARANOID SCHIZOPHRENICS [J].
ARATO, M ;
BAGDY, G ;
BLUMEL, F ;
PERENYI, A ;
RIHMER, Z .
PHARMACOPSYCHIATRIA, 1983, 16 (01) :19-22
[3]  
Arrufat FJ, 2000, AM J MED GENET, V96, P88, DOI 10.1002/(SICI)1096-8628(20000207)96:1<88::AID-AJMG18>3.0.CO
[4]  
2-V
[5]   Noradrenergic alpha-2 receptor agonists reverse working memory deficits induced by the anxiogenic drug, FG7142, in rats [J].
Birnbaum, SG ;
Podell, DM ;
Arnsten, AFT .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2000, 67 (03) :397-403
[6]   Dopamine β-hydroxylase:: two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variation [J].
Cubells, JF ;
van Kammen, DP ;
Kelley, ME ;
Anderson, GM ;
O'Connor, DT ;
Price, LH ;
Malison, R ;
Rao, PA ;
Kobayashi, K ;
Nagatsu, T ;
Gelernter, J .
HUMAN GENETICS, 1998, 102 (05) :533-540
[7]   A haplotype at the DBH locus, associated with low plasma dopamine β-hydroxylase activity, also associates with cocaine-induced paranoia [J].
Cubells, JF ;
Kranzler, HR ;
McCance-Katz, E ;
Anderson, GM ;
Malison, RT ;
Price, LH ;
Gelernter, J .
MOLECULAR PSYCHIATRY, 2000, 5 (01) :56-63
[8]  
DeLisi L E, 1980, Biol Psychiatry, V15, P895
[9]  
DUNNETTE J, 1976, AM J HUM GENET, V28, P155
[10]  
ENDICOTT J, 1976, ARCH GEN PSYCHIAT, V33, P766