Chen Jingchun, Bacanu Silviu-Alin, Yu Hui, Zhao Zhongming, Jia Peilin, Kendler Kenneth S, Kranzler Henry R, Gelernter Joel, Farrer Lindsay, Minica Camelia, Pool Rene, Milaneschi Yuri, Boomsma Dorret I, Penninx Brenda W J H, Tyndale Rachel F, Ware Jennifer J, Vink Jacqueline M, Kaprio Jaakko, Munafò Marcus, Chen Xiangning
Nevada Institute of Personalized Medicine, University of Nevada at Las Vegas, 4505 S. Maryland Parkway, Las Vegas, NV 89154, USA.
Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, 800 E. Leigh Street, Richmond, VA 23298, USA.
Sci Rep. 2016 May 10;6:25671. doi: 10.1038/srep25671.
It is well known that most schizophrenia patients smoke cigarettes. There are different hypotheses postulating the underlying mechanisms of this comorbidity. We used summary statistics from large meta-analyses of plasma cotinine concentration (COT), Fagerström test for nicotine dependence (FTND) and schizophrenia to examine the genetic relationship between these traits. We found that schizophrenia risk scores calculated at P-value thresholds of 5 × 10(-3) and larger predicted FTND and cigarettes smoked per day (CPD), suggesting that genes most significantly associated with schizophrenia were not associated with FTND/CPD, consistent with the self-medication hypothesis. The COT risk scores predicted schizophrenia diagnosis at P-values of 5 × 10(-3) and smaller, implying that genes most significantly associated with COT were associated with schizophrenia. These results implicated that schizophrenia and FTND/CPD/COT shared some genetic liability. Based on this shared liability, we identified multiple long non-coding RNAs and RNA binding protein genes (DA376252, BX089737, LOC101927273, LINC01029, LOC101928622, HY157071, DA902558, RBFOX1 and TINCR), protein modification genes (MANBA, UBE2D3, and RANGAP1) and energy production genes (XYLB, MTRF1 and ENOX1) that were associated with both conditions. Further analyses revealed that these shared genes were enriched in calcium signaling, long-term potentiation and neuroactive ligand-receptor interaction pathways that played a critical role in cognitive functions and neuronal plasticity.
众所周知,大多数精神分裂症患者吸烟。有不同的假说来推测这种共病现象的潜在机制。我们使用了来自血浆可替宁浓度(COT)、尼古丁依赖的Fagerström测试(FTND)和精神分裂症的大型荟萃分析的汇总统计数据,来研究这些性状之间的遗传关系。我们发现,在P值阈值为5×10⁻³及更大时计算出的精神分裂症风险评分预测了FTND和每日吸烟量(CPD),这表明与精神分裂症最显著相关的基因与FTND/CPD无关,这与自我药疗假说一致。COT风险评分在P值为5×10⁻³及更小时预测了精神分裂症诊断,这意味着与COT最显著相关的基因与精神分裂症有关。这些结果表明精神分裂症与FTND/CPD/COT存在一些共同的遗传易感性。基于这种共同易感性,我们鉴定出了多个与这两种情况都相关的长链非编码RNA和RNA结合蛋白基因(DA376252、BX089737、LOC101927273、LINC01029、LOC101928622、HY157071、DA902558、RBFOX1和TINCR)、蛋白质修饰基因(MANBA、UBE2D3和RANGAP1)以及能量产生基因(XYLB、MTRF1和ENOX1)。进一步分析表明,这些共享基因在钙信号传导、长时程增强和神经活性配体-受体相互作用途径中富集,这些途径在认知功能和神经元可塑性中起关键作用。