Blackwood D H R, Thiagarajah T, Malloy P, Pickard B S, Muir W J
Division of Psychiatry, School of Molecular and Clinical Medicine, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh EH10 5HF, UK.
Neurotox Res. 2008 Oct;14(2-3):113-20. doi: 10.1007/BF03033803.
Genetic factors contribute to schizophrenia and bipolar disorder, and linkage and association studies have been successful in identifying several candidate genes. However these genes explain only a very small part of the total population risk and the psychoses appear to be very heterogeneous with several models of genetic inheritance relevant to different groups of patients, including some cases caused by multiple common genetic variants, while others are single gene disorders. Studying chromosomal abnormalities is a useful strategy for identifying genes in illness, and patients with both mental retardation and psychosis form a special group where large chromosomal abnormalities detected by routine cytogenetic analysis are more prevalent than in patients with schizophrenia or bipolar disorder alone, or in the general population. Studying these patients provides valuable opportunities to identify genes contributing to psychoses. This review of the literature on large chromosomal rearrangements in patients with mental retardation and psychotic illness illustrates how schizophrenia and bipolar phenotypes are associated with a large number of different chromosomal disruptions. Recent genome wide association studies have identified an excess of small chromosomal deletions and duplications in schizophrenia, adding further support to the importance of chromosomal structural variation in psychotic illness. The genes GRIK4 and NPAS3, each associated with psychosis in patients with mental retardation are discussed to illustrate the value of rare cytogenetic events as a means to signpost neurobiological pathways of general importance for illness in the wider population.
遗传因素在精神分裂症和双相情感障碍中起作用,连锁和关联研究已成功鉴定出多个候选基因。然而,这些基因仅解释了总人口风险中的极小部分,而且精神病似乎具有高度异质性,存在多种与不同患者群体相关的遗传遗传模式,包括一些由多个常见遗传变异引起的病例,而其他则是单基因疾病。研究染色体异常是识别疾病相关基因的一种有用策略,智力迟钝和精神病患者构成了一个特殊群体,通过常规细胞遗传学分析检测到的大染色体异常在该群体中比仅患有精神分裂症或双相情感障碍的患者或普通人群中更为普遍。研究这些患者为识别导致精神病的基因提供了宝贵机会。这篇关于智力迟钝和精神病患者大染色体重排的文献综述说明了精神分裂症和双相情感障碍表型如何与大量不同的染色体破坏相关联。最近的全基因组关联研究已在精神分裂症中发现了过多的小染色体缺失和重复,进一步支持了染色体结构变异在精神病中的重要性。讨论了分别与智力迟钝患者的精神病相关的基因GRIK4和NPAS3,以说明罕见细胞遗传学事件作为一种手段来标示对更广泛人群中疾病具有普遍重要性的神经生物学途径的价值。