No Association of Dysbindin With Symptom Factors of Schizophrenia in an Irish Case-Control Sample

被引:3
|
作者
Bergen, Sarah E. [1 ,2 ]
Fanous, Agman H. [3 ,4 ,5 ]
Ku, Po-Hsiu [6 ]
Wormley, Brandon K. [3 ]
O'Neill, F. Anthony [7 ]
Walsh, Dermot [8 ]
Riley, Brien P. [2 ,3 ]
Kendler, Kenneth S. [2 ,3 ]
机构
[1] Virginia Commonwealth Univ, Med Coll Virginia, Dept Human Genet, Virginia Inst Psychiat & Behav Genet, Richmond, VA 23219 USA
[2] Virginia Commonwealth Univ, Dept Human & Mol Genet, Richmond, VA 23219 USA
[3] Virginia Commonwealth Univ, Dept Psychiat, Richmond, VA USA
[4] Washington VA Med Ctr, Washington, DC USA
[5] Georgetown Univ, Med Ctr, Dept Psychiat, Washington, DC 20007 USA
[6] Natl Taiwan Univ, Dept Publ Hlth, Taipei 10764, Taiwan
[7] Queens Univ, Dept Mental Hlth, Belfast, Antrim, Ireland
[8] Hlth Res Board, Dublin, Ireland
关键词
modifier; sequential addition; negative symptoms; BINDING PROTEIN-1 DTNBP1; HIGH-RISK HAPLOTYPE; GENE DTNBP1; HIPPOCAMPAL-FORMATION; NEGATIVE SYMPTOMS; CANDIDATE GENES; 6P22.3; GENE; SUPPORT; LOCUS; IDENTIFICATION;
D O I
10.1002/ajmg.b.31029
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Robust associations between the dysbindin gene (DTNBP1) and schizophrenia have been demonstrated in many but not all samples, and evidence that this gene particularly predisposes to negative symptoms in this illness has been presented. The current study sought to replicate the previously reported negative symptom associations in an Irish case-control sample. Association between dysbindin and schizophrenia has been established in this cohort, and a factor analysis of the assessed symptoms yielded three factors, Positive, Negative, and Schneiderian. The sequential addition method was applied using UNPHASED to assess the relationship between these symptom factors and the high-risk haplotype. No associations were detected for any of the symptom factors indicating that the dysbindin risk haplotype does not predispose to a particular group of symptoms in this sample. Several possibilities, such as differing risk haplotypes, may explain this finding. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:700 / 705
页数:6
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