Putative psychosis genes in the prefrontal cortex: combined analysis of gene expression microarrays

被引:49
作者
Choi, Kwang Ho [1 ]
Elashoff, Michael [2 ]
Higgs, Brandon W. [2 ]
Song, Jonathan [1 ]
Kim, Sanghyeon [1 ]
Sabunciyan, Sarven [3 ]
Diglisic, Suad [1 ]
Yolken, Robert H. [3 ]
Knable, Michael B. [4 ]
Torrey, E. Fuller [4 ]
Webster, Maree J. [1 ]
机构
[1] Stanley Lab Brain Res, Rockville, MD 20850 USA
[2] Elashoff Consulting, Redwood City, CA 94065 USA
[3] Johns Hopkins Univ, Sch Med, Stanley Lab Dev Neurovirol, Baltimore, MD 21287 USA
[4] Stanley Med Res Inst, Chevy Chase, MD 20815 USA
关键词
D O I
10.1186/1471-244X-8-87
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Recent studies have shown similarities between schizophrenia and bipolar disorder in phenotypes and in genotypes, and those studies have contributed to an ongoing re-evaluation of the traditional dichotomy between schizophrenia and bipolar disorder. Bipolar disorder with psychotic features may be closely related to schizophrenia and therefore, psychosis may be an alternative phenotype compared to the traditional diagnosis categories. Methods: We performed a cross-study analysis of 7 gene expression microarrays that include both psychosis and non-psychosis subjects. These studies include over 400 microarray samples (163 individual subjects) on 3 different Affymetrix microarray platforms. Results: We found that 110 transcripts are differentially regulated (p < 0.001) in psychosis after adjusting for confounding variables with a multiple regression model. Using a quantitative PCR, we validated a set of genes such as up-regulated metallothioneins (MT1E, MT1F, MT1H, MT1K, MT1X, MT2A and MT3) and down-regulated neuropeptides (SST, TAC1 and NPY) in the dorsolateral prefrontal cortex of psychosis patients. Conclusion: This study demonstrates the advantages of cross-study analysis in detecting consensus changes in gene expression across multiple microarray studies. Differential gene expression between individuals with and without psychosis suggests that psychosis may be a useful phenotypic variable to complement the traditional diagnosis categories.
引用
收藏
页数:14
相关论文
共 73 条
[1]   Molecular evidence for increased expression of genes related to immune and chaperone function in the prefrontal cortex in schizophrenia [J].
Arion, Dominique ;
Unger, Travis ;
Lewis, David A. ;
Levitt, Pat ;
Mirnics, Karoly .
BIOLOGICAL PSYCHIATRY, 2007, 62 (07) :711-721
[2]   Gene expression profiling in the post-mortem human brain - no cause for dismay [J].
Bahn, S ;
Augood, S ;
Standaert, DG ;
Starkey, M ;
Emson, PC .
JOURNAL OF CHEMICAL NEUROANATOMY, 2001, 22 (1-2) :79-94
[3]   The pathomorphology of schizophrenia and mood disorders: similarities and differences [J].
Baumann, B ;
Bogerts, B .
SCHIZOPHRENIA RESEARCH, 1999, 39 (02) :141-148
[4]   Gene expression in the etiology of schizophrenia [J].
Bray, Nicholas J. .
SCHIZOPHRENIA BULLETIN, 2008, 34 (03) :412-418
[5]   Meta-analysis of microarray results: challenges, opportunities, and recommendations for standardization [J].
Cahan, Patrick ;
Rovegno, Felicia ;
Mooney, Denise ;
Newman, John C. ;
St. Laurent, Georges, III ;
McCaffrey, Timothy A. .
GENE, 2007, 401 (1-2) :12-18
[6]   Tachykinins and neuropsychiatric disorders [J].
Chahl, Loris A. .
CURRENT DRUG TARGETS, 2006, 7 (08) :993-1003
[7]   Mutation analysis of the human NR4A2 gene, an essential gene for midbrain dopaminergic neurogenesis, in schizophrenic patients [J].
Chen, YH ;
Tsai, MT ;
Shaw, CK ;
Chen, CH .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (08) :753-757
[8]   Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology [J].
Craddock, N ;
O'Donovan, MC ;
Owen, MJ .
SCHIZOPHRENIA BULLETIN, 2006, 32 (01) :9-16
[10]   Gene expression profiling in Brodmann's area 46 from subjects with schizophrenia [J].
Dean, Brian ;
Keriakous, Dahlia ;
Scarr, Elizabeth ;
Thomas, Elizabeth A. .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 2007, 41 (04) :308-320