The catechol O-methyltransferase Val158Met polymorphism is not associated with broad-based cognititive functioning in schizophrenia

被引:11
作者
Dickerson, Faith B.
BoronoW, John J.
Stallings, Cassie
Origoni, Andrea E.
SullenS, Anne
Yolken, Robert H.
机构
[1] Sheppard Pratt Hlth Syst, Stanley Res Program Sheppard Pratt, Baltimore, MD 21204 USA
[2] Johns Hopkins Univ, Sch Med, Stanley Neurovirol Lab, Baltimore, MD 21207 USA
关键词
schizophrenia; genetic; COMT; cognition;
D O I
10.1016/j.schres.2007.05.021
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: A valine/methionine polymorphism of the catechol O-methyltransferase gene at the nucleotide which encodes amino acid val or met at position 158 in the protein (COMT Vall58Met polymorphism) has been associated with deficits in executive functioning in schizophrenia in some studies. The association between the COMT polymorphism and other cognitive domains has been the focus of only limited investigation. Methods: We measured COMT Vall58Met genotypes in N=364 individuals with schizophrenia. Cognitive functioning was assessed with the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS). We employed univariate and multivariate analyses of variance to determine the association between COMT genotypes and the RBANS index and individual test scores. Results: There was no significant association between the COMT Vall58Met genotypes and any of the RBANS index or individual test scores measured in either univariate or multivariate analyses (all p>.3). Conclusion: Based on the results in our sample, the catechol O-methyltransferase Vall58Met polymorphism is not associated with broad-based cognitive functioning in schizophrenia. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 92
页数:6
相关论文
共 36 条
[21]  
Kay S.R., 1991, POSITIVE NEGATIVE SY
[22]   Cognitive impairments associated with formal thought disorder in people with schizophrenia [J].
Kerns, JG ;
Berenbaum, H .
JOURNAL OF ABNORMAL PSYCHOLOGY, 2002, 111 (02) :211-224
[23]  
Leung A, 2000, ACTA PSYCHIAT SCAND, V101, P3
[24]   Screening for cognitive functioning in psychiatric outpatients with schizophrenia, alcohol dependence, and dual diagnosis [J].
Manning, Victoria ;
Wanigaratne, Shamil ;
Best, David ;
Strathdee, Geraldine ;
Schrover, Isabella ;
Gossop, Michael .
SCHIZOPHRENIA RESEARCH, 2007, 91 (1-3) :151-158
[25]   A meta-analysis and critical review of the effects of conventional neuroleptic treatment on cognition in schizophrenia: Opening a closed book [J].
Mishara, AL ;
Goldberg, TE .
BIOLOGICAL PSYCHIATRY, 2004, 55 (10) :1013-1022
[26]   New evidence of association between COMT gene and prefrontal neurocognitive from sibling function in healthy individuals pairs discordant for psychosis [J].
Rosa, A ;
Peralta, V ;
Cuesta, MJ ;
Zarzuela, A ;
Serrano, F ;
Martínez-Larrea, A ;
Fañanás, L .
AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (06) :1110-1112
[27]  
RRANDOLPH C, 1998, RBANS MANAUAL REPEAT
[28]   Plexin B3 is genetically associated with verbal performance and white matter volume in human brain [J].
Rujescu, D. ;
Meisenzahl, E. M. ;
Krejcova, S. ;
Giegling, I. ;
Zetzsche, T. ;
Reiser, M. ;
Born, C. M. ;
Moeller, H-J ;
Veske, A. ;
Gal, A. ;
Finckh, U. .
MOLECULAR PSYCHIATRY, 2007, 12 (02) :190-194
[29]   Role of dopamine D3 receptor (DRD3) and dopamine transporter (DAT) polymorphism in cognitive dysfunctions and therapeutic response to atypical antipsychotics in patients with schizophrenia [J].
Szekeres, G ;
Kéri, S ;
Juhász, A ;
Rimanóczy, A ;
Szendi, I ;
Czimmer, C ;
Janka, Z .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 124B (01) :1-5
[30]   Lack of influence of COMT and NET genes variants on executive functions in schizophrenic and bipolar patients, their first-degree relatives and controls [J].
Szoke, A. ;
Schurhoff, F. ;
Meary, A. ;
Mathieu, F. ;
Chevalier, F. ;
Trandafir, A. ;
Alter, C. ;
Roy, I. ;
Bellivier, F. ;
Leboyer, M. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B (05) :504-512