Hodgkinson Colin A, Goldman David, Ducci Francesca, DeRosse Pamela, Caycedo Daniel A, Newman Emily R, Kane John M, Roy Alec, Malhotra Anil K
Section of Human Neurogenetics, Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, Bethesda, MD, USA.
Neuropsychopharmacology. 2007 Jan;32(1):190-6. doi: 10.1038/sj.npp.1301177. Epub 2006 Aug 16.
Schizophrenia is a complex psychiatric disorder with both genetic and environmental components and is thought to be in part neurodevelopmental in origin. The DISC1 gene has been linked to schizophrenia in two independent Caucasian populations. The DISC1 protein interacts with a variety of proteins including FEZ1, the mammalian homolog of the Caenorhabditis elegans unc-76 protein, which is involved in axonal outgrowth. Variation at the FEZ1 gene has been associated with schizophrenia in a large Japanese cohort. In this study, nine SNP markers at the FEZ1 locus were genotyped in two populations. A North American Caucasian cohort of 212 healthy controls, 178 schizophrenics, 79 bipolar disorder, and 58 with schizoaffective disorder, and an African American cohort of 133 healthy controls, 162 schizophrenics, and 28 with schizoaffective disorder. No association to schizophrenia, bipolar disorder or schizoaffective disorder was found for any of the nine markers typed in these populations at the allelic or the genotypic level. Additionally no association was found in either population between specific haplotypes and any of the psychiatric disorders. Variation at the FEZ1 locus does not play a significant role in the etiology of schizophrenia, bipolar disorder or schizoaffective disorder in North American Caucasian or African American populations.Neuropsychopharmacology (2007) 32, 190-196. doi:10.1038/sj.npp.1301177; published online 16 August 2006.
精神分裂症是一种具有遗传和环境因素的复杂精神障碍,被认为部分起源于神经发育。DISC1基因已在两个独立的白种人群体中与精神分裂症相关联。DISC1蛋白与多种蛋白质相互作用,包括FEZ1,它是秀丽隐杆线虫unc-76蛋白的哺乳动物同源物,参与轴突生长。FEZ1基因的变异在一个大型日本队列中与精神分裂症有关。在本研究中,对两个群体的FEZ1基因座的9个单核苷酸多态性(SNP)标记进行了基因分型。一个北美白种人队列包括212名健康对照、178名精神分裂症患者、79名双相情感障碍患者和58名精神分裂症情感障碍患者,以及一个非裔美国人队列包括133名健康对照、162名精神分裂症患者和28名精神分裂症情感障碍患者。在这些群体中,对9个标记中的任何一个在等位基因或基因型水平上均未发现与精神分裂症、双相情感障碍或精神分裂症情感障碍相关联。此外,在任何一个群体中,特定单倍型与任何精神障碍之间均未发现关联。FEZ1基因座的变异在北美白种人或非裔美国人人群的精神分裂症、双相情感障碍或精神分裂症情感障碍的病因中不发挥重要作用。《神经精神药理学》(2007年)32卷,190 - 196页。doi:10.1038/sj.npp.1301177;2006年8月16日在线发表。