No association of the C677T methylenetetrahydrofolate reductase polymorphism with schizophrenia

被引:22
作者
Philibert, Robert
Gunter, Tracy
Hollenbeck, Nancy
Adams, William J.
Bohle, Phillip
Packer, Hans
Sandhu, Harinder
机构
[1] Univ Iowa, Dept Psychiat, Iowa City, IA 52242 USA
[2] Univ Iowa, Program Neurosci, Iowa City, IA 52242 USA
关键词
genetics; methylenetetrahydrofolate reductase; schizophrenia;
D O I
10.1097/01.ypg.0000242192.28526.fa
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Some serological and genetic studies have suggested that alterations in folate metabolism are associated with increased vulnerability to schizophrenia. In particular, these findings are most striking for the role of a putatively functional variant (C677T) in the methylenetetrahydrofolate reductase (MTHFR) gene. To test the hypothesis that the T allele and the TT genotype are risk factors for psychosis, we genotyped the C677T polymorphism in 206 participants with schizophrenia or schizoaffective disorder and 359 participants from a population control sample. Neither the T allele nor the TT genotype was associated with increased risk for schizophrenia. These results do not support a role for the C677T MTHFR variant in schizophrenia. Psychiatr Genet 16:221-223 (c) 2006 Lippincott Williams & Wilkins.
引用
收藏
页码:221 / 223
页数:3
相关论文
共 15 条
[1]   Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients:: A preliminary report [J].
Abdolmaleky, HM ;
Cheng, KH ;
Russo, A ;
Smith, CL ;
Faraone, SV ;
Wilcox, M ;
Shafa, R ;
Glatt, SJ ;
Nguyen, G ;
Ponte, JF ;
Thiagalingam, S ;
Tsuang, MT .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 134B (01) :60-66
[2]  
Fleiss J. L., 1981, Statistical Methods for Rates and Proportions, V2nd
[3]   The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia [J].
Guenther B.D. ;
Sheppard C.A. ;
Tran P. ;
Rozen R. ;
Matthews R.G. ;
Ludwig M.L. .
Nature Structural Biology, 1999, 6 (4) :359-365
[4]  
Hartl D.L., 1997, PRINCIPLES POPULATIO
[5]  
LECKMAN JF, 1982, ARCH GEN PSYCHIAT, V39, P879
[6]   A meta-analysis of the MTHFR C677T polymorphism and schizophrenia risk [J].
Lewis, SJ ;
Zammit, S ;
Gunnell, D ;
Smith, GD .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 135B (01) :2-4
[7]   Hyperhomocysteinemia, methylenetetrahydrofolate reductase 677TT genotype, and the risk for schizophrenia: A Dutch population based case-control study [J].
Muntjewerff, JW ;
Hoogendoorn, MLC ;
Kahn, RS ;
Sinke, RJ ;
Den Heijer, M ;
Kluijtmans, LAJ ;
Blom, HJ .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 135B (01) :69-72
[8]  
MUNTJEWERFF JW, 2005, MOL PSYCHIAT 0920
[9]   DIAGNOSTIC INTERVIEW FOR GENETIC-STUDIES - RATIONALE, UNIQUE FEATURES, AND TRAINING [J].
NURNBERGER, JI ;
BLEHAR, MC ;
KAUFMANN, CA ;
YORKCOOLER, C ;
SIMPSON, SG ;
HARKAVYFRIEDMAN, J ;
SEVERE, JB ;
MALASPINA, D ;
REICH, T ;
MILLER, M ;
BOWMAN, ES ;
DEPAULO, JR ;
CLONINGER, CR ;
ROBINSON, G ;
MODLIN, S ;
GERSHON, ES ;
MAXWELL, E ;
GUROFF, JJ ;
KIRCH, D ;
WYNNE, D ;
BERG, K ;
TSUANG, MT ;
FARAONE, SV ;
PEPPLE, JR ;
RITZ, AL .
ARCHIVES OF GENERAL PSYCHIATRY, 1994, 51 (11) :849-859
[10]  
Philibert RA, 2001, AM J MED GENET, V105, P130, DOI 10.1002/1096-8628(20010108)105:1<130::AID-AJMG1076>3.3.CO