Intron 12 in NTRK3 is associated with bipolar disorder

被引:20
作者
Athanasiu, Lavinia [1 ,2 ,3 ]
Mattingsdal, Morten [2 ,3 ]
Melle, Ingrid [2 ,3 ]
Inderhaug, Elin [2 ]
Lien, Trude [1 ]
Agartz, Ingrid [3 ,4 ]
Lorentzen, Steinar [3 ,5 ]
Morken, Gunnar [6 ,7 ]
Andreassen, Ole A. [2 ,3 ]
Djurovic, Srdjan [1 ,3 ]
机构
[1] Oslo Univ Hosp Ulleval, Dept Med Genet, N-0407 Oslo, Norway
[2] Oslo Univ Hosp Ulleval, Dept Psychiat, N-0407 Oslo, Norway
[3] Univ Oslo, Inst Psychiat, Oslo, Norway
[4] Diakonhjemmet Hosp, Dept Psychiat Res, Oslo, Norway
[5] Oslo Univ Hosp Aker, Dept Psychiat, Oslo, Norway
[6] Norwegian Univ Technol & Sci, Ostmarka Psychiat Dept, St Olavs Hosp, Trondheim, Norway
[7] Norwegian Univ Technol & Sci, Inst Neurosci, Trondheim, Norway
关键词
NTRK3; SNP; Bipolar disorders; CHROMOSOME; 15Q25-26; NEUROTROPHIC FACTOR; GENE POLYMORPHISMS; TRANSGENIC MICE; SCHIZOPHRENIA; SUSCEPTIBILITY; POPULATION; RATIONALE; HISTORY; CORTEX;
D O I
10.1016/j.psychres.2010.05.011
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Based on the important role of neurotrophic factors in brain development and plasticity and reports of association between schizophrenia and the gene neurotrophic tyrosine kinase receptor 3 (NTRK3), we investigated associations of bipolar disorder with polymorphisms in NTRK3. Recently, our group reported evidence for a possible association of NTRK3 polymorphisms with hippocampal function and schizophrenia. In the present study, we used a homogenous Norwegian case-control sample (the TOP study) consisting of 194 patients diagnosed with bipolar disorder and 336 healthy controls genotyped on the Affymetrix Genome-wide Human SNP Array 6.0. In total 149 markers were investigated for SNP-disease association. Polymorphisms in over 20 markers were nominally associated with bipolar disorder, covering intron 5 to intron 12. Interestingly, our markers appeared to be located close or within the linkage regions reported in schizophrenia, early-onset major depressive disorder and eating disorder, supporting the hypothesis that some genes influence risk beyond traditional diagnostic boundaries. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:358 / 362
页数:5
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