Lencz T, Morgan T V, Athanasiou M, Dain B, Reed C R, Kane J M, Kucherlapati R, Malhotra A K
Department of Psychiatry Research, The Zucker Hillside Hospital, Division of the North Shore-Long Island Jewish Health System, Glen Oaks, NY 11004, USA.
Mol Psychiatry. 2007 Jun;12(6):572-80. doi: 10.1038/sj.mp.4001983. Epub 2007 Mar 20.
Schizophrenia is a strongly heritable disorder, and identification of potential candidate genes has accelerated in recent years. Genomewide scans have identified multiple large linkage regions across the genome, with fine-mapping studies and other investigations of biologically plausible targets demonstrating several promising candidate genes of modest effect. The recent introduction of technological platforms for whole-genome association (WGA) studies can provide an opportunity to rapidly identify novel targets, although no WGA studies have been reported in the psychiatric literature to date. We report results of a case-control WGA study in schizophrenia, examining approximately 500 000 markers, which revealed a strong effect (P=3.7 x 10(-7)) of a novel locus (rs4129148) near the CSF2RA (colony stimulating factor, receptor 2 alpha) gene in the pseudoautosomal region. Sequencing of CSF2RA and its neighbor, IL3RA (interleukin 3 receptor alpha) in an independent case-control cohort revealed both common intronic haplotypes and several novel, rare missense variants associated with schizophrenia. The presence of cytokine receptor abnormalities in schizophrenia may help explain prior epidemiologic data relating the risk for this illness to altered rates of autoimmune disorders, prenatal infection and familial leukemia.
精神分裂症是一种具有高度遗传性的疾病,近年来对潜在候选基因的识别进程加快。全基因组扫描已在全基因组中识别出多个大的连锁区域,精细定位研究以及对生物学上合理靶点的其他调查显示了几个有前景的、效应中等的候选基因。全基因组关联(WGA)研究技术平台的近期引入为快速识别新靶点提供了机会,尽管迄今为止精神科文献中尚未报道过WGA研究。我们报告了一项精神分裂症病例对照WGA研究的结果,检测了约50万个标记,结果显示在假常染色体区域中靠近CSF2RA(集落刺激因子,受体2α)基因的一个新位点(rs4129148)有显著效应(P = 3.7 x 10^(-7))。在一个独立的病例对照队列中对CSF2RA及其邻近基因IL3RA(白细胞介素3受体α)进行测序,发现了与精神分裂症相关的常见内含子单倍型以及几个新的、罕见的错义变异。精神分裂症中细胞因子受体异常的存在可能有助于解释先前的流行病学数据,这些数据将该疾病的风险与自身免疫性疾病、产前感染和家族性白血病发生率的改变联系起来。