Jackson Kia J, Fanous Ayman H, Chen Jingchun, Kendler Kenneth S, Chen Xiangning
Department of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia 23219, USA.
Psychiatr Genet. 2013 Feb;23(1):20-8. doi: 10.1097/YPG.0b013e32835bd5f1.
Rates of tobacco smoking are significantly higher in patients with schizophrenia compared with the general population. The underlying mechanism for this comorbidity is unclear. One hypothesis is that there are common genetic factors that predispose to both nicotine dependence (ND) and schizophrenia. To investigate this hypothesis, we examined the association of the 15q25 gene cluster, the most significant candidate region to date implicated in ND and smoking behavior, with schizophrenia and bipolar disorder.
Five variants in the 15q25 gene cluster (rs951266, rs16969968, rs1051730, rs8040868, and rs17477223) were selected to test for association with schizophrenia diagnosis, bipolar disorder diagnosis, and the presence of negative symptoms of schizophrenia. Effects of the variants on 15q25 gene expression were analyzed using publically available postmortem brain expression data.
A meta-analysis revealed four markers associated with risk for schizophrenia and bipolar disorder (rs951266, rs16969968, rs8040868, and rs17477223), and with the presence of negative symptoms of schizophrenia (rs951266, rs1051730, rs8040868, and rs17477223). The associations were in the same direction as that found for ND. Gene expression analysis indicated an association between genotypes of the rs1051730 variant and CHRNA5 expression in brain and peripheral blood mononuclear cells, and with the rs16969968 and rs17477223 variants in brain.
Variants in the 15q25 gene cluster are associated with risk for schizophrenia/bipolar illness, negative symptoms of schizophrenia, and influence CHRNA5 expression in the brain and peripheral blood mononuclear cells. These results are consistent with the notion that there are genetic mechanisms common to schizophrenia, ND, and bipolar disorder.
与普通人群相比,精神分裂症患者的吸烟率显著更高。这种共病的潜在机制尚不清楚。一种假说认为,存在共同的遗传因素使人易患尼古丁依赖(ND)和精神分裂症。为了研究这一假说,我们检测了15q25基因簇(迄今为止与ND和吸烟行为相关的最显著候选区域)与精神分裂症和双相情感障碍之间的关联。
选择15q25基因簇中的五个变体(rs951266、rs16969968、rs1051730、rs8040868和rs17477223)来检测与精神分裂症诊断、双相情感障碍诊断以及精神分裂症阴性症状的存在之间的关联。利用公开的尸检脑表达数据,分析这些变体对15q25基因表达的影响。
一项荟萃分析显示,四个标记与精神分裂症和双相情感障碍的风险相关(rs951266、rs16969968、rs8040868和rs17477223),并与精神分裂症阴性症状的存在相关(rs951266、rs1051730、rs8040868和rs17477223)。这些关联与在ND中发现的关联方向相同。基因表达分析表明,rs1051730变体的基因型与脑和外周血单核细胞中的CHRNA5表达之间存在关联,并且与脑中的rs16969968和rs17477223变体存在关联。
15q25基因簇中的变体与精神分裂症/双相情感障碍的风险、精神分裂症的阴性症状相关,并影响脑和外周血单核细胞中的CHRNA5表达。这些结果与精神分裂症、ND和双相情感障碍存在共同遗传机制的观点一致。