Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia:: working memory, frontal lobe MRI morphology and frontal cerebral blood flow

被引:160
作者
Ho, BC
Wassink, TH
O'Leary, DS
Sheffield, VC
Andreasen, NC
机构
[1] Univ Iowa, Dept Psychiat, Roy J & Lucille A Carver Coll Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Howard Hughes Med Inst, Dept Pediat, Div Mol Genet, Iowa City, IA 52242 USA
[3] MIND Inst, Albuquerque, NM USA
[4] Univ New Mexico, Dept Psychiat, Albuquerque, NM 87131 USA
关键词
endophenotype; dopamine; MRI; candidate gene; association study; PET;
D O I
10.1038/sj.mp.4001616
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The catechol-O-methyl transferase ( COMT) gene is considered a leading schizophrenia candidate gene. Although its role in increasing schizophrenia susceptibility has been conflicting, recent studies suggest the valine allele may contribute to poor cognitive function in schizophrenia. (VM)-M-158 COMT genotype was obtained on 159 schizophrenia patients and 84 healthy controls. The effects of COMT genotype on four measures of working memory/executive functions (Wisconsin Card Sorting, digit span backward, Trail Making and N-back tests) and on MRI frontal brain volumes were examined. Genotype distributions were not significantly different between patients and controls. There were no significant genotype or genotype-by-group effects on any working memory/executive function measures. No genotype or genotype-by-diagnosis interaction effects were found with MRI frontal lobe volumes. Randomization analyses using [O-15]H2O positron emission tomography ( PET) cerebral blood flow data found Val/Val patients had higher frontal lobe activation than Met/Met patients while performing the one-back task. Overall, these findings do not support a major role for COMT in increasing susceptibility for schizophrenia or in mediating frontal lobe function. Age-related changes and phenotypic heterogeneity of schizophrenia may influence the complex relationships between COMT genotype and cognition.
引用
收藏
页码:287 / 298
页数:12
相关论文
共 123 条
[1]  
Almasy L, 2001, AM J MED GENET, V105, P42, DOI 10.1002/1096-8628(20010108)105:1<42::AID-AJMG1055>3.3.CO
[2]  
2-0
[3]   Genetic structure of spatial and verbal working memory [J].
Ando, J ;
Ono, Y ;
Wright, MJ .
BEHAVIOR GENETICS, 2001, 31 (06) :615-624
[4]   Schizophrenia: the fundamental questions [J].
Andreasen, NC .
BRAIN RESEARCH REVIEWS, 2000, 31 (2-3) :106-112
[5]  
ANDREASEN NC, 1992, ARCH GEN PSYCHIAT, V49, P615
[6]   TECHNIQUES FOR MEASURING SULCAL GYRAL PATTERNS IN THE BRAIN AS VISUALIZED THROUGH MAGNETIC-RESONANCE SCANNING - BRAINPLOT AND BRAINMAP [J].
ANDREASEN, NC ;
HARRIS, G ;
CIZADLO, T ;
ARNDT, S ;
OLEARY, DS ;
SWAYZE, V ;
FLAUM, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :93-97
[7]  
ANDREASEN NC, 1992, J NEUROPSYCH CLIN N, V4, P125
[8]   Automatic atlas-based volume estimation of human brain regions from MR images [J].
Andreasen, NC ;
Rajarethinam, R ;
Cizadlo, T ;
Arndt, S ;
Swayze, VW ;
Flashman, LA ;
OLeary, DS ;
Ehrhardt, JC ;
Yuh, WTC .
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 1996, 20 (01) :98-106
[9]  
ANDREASEN NC, 1993, J NEUROPSYCH CLIN N, V5, P121
[10]   Screening for 22q11 deletions in a schizophrenia population [J].
Arinami, T ;
Ohtsuki, T ;
Takase, K ;
Shimizu, H ;
Yoshikawa, T ;
Horigome, H ;
Nakayama, J ;
Toru, M .
SCHIZOPHRENIA RESEARCH, 2001, 52 (03) :167-170