Tiwari Arun K, Zai Clement C, Müller Daniel J, Kennedy James L
Neurogenetics section, Neuroscience department, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Dialogues Clin Neurosci. 2010;12(3):289-303. doi: 10.31887/DCNS.2010.12.3/atiwari.
Understanding the genetic basis of schizophrenia continues to be major challenge. The research done during the last two decades has provided several candidate genes which unfortunately have not been consistently replicated across or within a population. The recent genome-wide association studies (GWAS) and copy number variation (CNV) studies have provided important evidence suggesting a role of both common and rare large CNVs in schizophrenia genesis. The burden of rare copy number variations appears to be increased in schizophrenia patients. A consistent observation among the GWAS studies is the association with schizophrenia of genetic markers in the major histocompatibility complex (6p22.1)-containing genes including NOTCH4 and histone protein loci. Molecular genetic studies are also demonstrating that there is more overlap between the susceptibility genes for schizophrenia and bipolar disorder than previously suspected. In this review we summarize the major findings of the past decade and suggest areas of future research.
了解精神分裂症的遗传基础仍然是一项重大挑战。过去二十年的研究已经提供了几个候选基因,但遗憾的是,这些基因在不同人群或同一人群内部并未得到一致的重复验证。最近的全基因组关联研究(GWAS)和拷贝数变异(CNV)研究提供了重要证据,表明常见和罕见的大片段CNV在精神分裂症发病机制中均起作用。精神分裂症患者中罕见拷贝数变异的负担似乎有所增加。GWAS研究中一个一致的观察结果是,主要组织相容性复合体(6p22.1)中包含NOTCH4和组蛋白基因座的基因中的遗传标记与精神分裂症有关。分子遗传学研究还表明,精神分裂症和双相情感障碍的易感基因之间的重叠比以前认为的更多。在这篇综述中,我们总结了过去十年的主要发现,并提出了未来研究的方向。