NO ASSOCIATION BETWEEN SCHIZOPHRENIA AND POLYMORPHISMS WITHIN THE GENES FOR DEBRISOQUINE 4-HYDROXYLASE (CYP2D6) AND THE DOPAMINE TRANSPORTER (DAT)

被引:40
作者
DANIELS, J
WILLIAMS, J
ASHERSON, P
MCGUFFIN, P
OWEN, M
机构
[1] UNIV WALES COLL MED,DEPT PSYCHOL MED,CARDIFF CF4 4XN,S GLAM,WALES
[2] UNIV WALES COLL MED,DEPT MED GENET,CARDIFF CF4 4XN,S GLAM,WALES
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 60卷 / 01期
基金
英国医学研究理事会;
关键词
PARKINSONS DISEASE; MUTATIONS; ASSOCIATION STUDY; POLYMORPHISMS; CANDIDATE GENES;
D O I
10.1002/ajmg.1320600115
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
It has been suggested that the cytochrome P450 mono-oxygenase, debrisoquine 4-hydrogylase, is involved in the catabolism and processing of neurotransmitters subsequent to their reuptake into target cells. It is also thought to be related to the dopamine transporter that acts to take released dopamine back up into presynaptic terminals. The present study used the association approach to test the hypothesis that mutations in the genes for debrisoquine 4-hydrogylase (CYP2D6) and the dopamine transporter (DAT) confer susceptibility to schizophrenia. There were no differences in allele or genotype frequencies between patients and controls ill the mutations causing the poor metaboliser phenotype in CYP2D6. In addition there was no association found between schizophrenia and a 48bp repeat within the 3' untranslated region of DAT. (C) 1995 Wiley Liss, Inc.
引用
收藏
页码:85 / 87
页数:3
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