Prasad Sarah E, Howley Sarah, Murphy Kieran C
Department of Psychiatry, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin 9, Republic of Ireland.
Dev Disabil Res Rev. 2008;14(1):26-34. doi: 10.1002/ddrr.5.
There is an overwhelming evidence that children and adults with 22q11.2 deletion syndrome (22q11.2DS) have a characteristic behavioral phenotype. In particular, there is a growing body of evidence that indicates an unequivocal association between 22q11.2DS and schizophrenia, especially in adulthood. Deletion of 22q11.2 is the third highest risk for the development of schizophrenia, with only a greater risk conferred by being the child of two parents with schizophrenia or the monozygotic co-twin of an affected individual. Both linkage and association studies of people with schizophrenia have implicated several susceptibility genes, of which three are in the 22q11.2 region; catechol-o-methyltransferase (COMT), proline dehydrogenase (PRODH), and Gnb1L. In addition, variation in Gnb1L is associated with the presence of psychosis in males with 22q11.2DS. In mouse models of 22q11.2DS, haploinsufficiency of Tbx1 and Gnb1L is associated with reduced prepulse inhibition, a schizophrenia endophenotype. The study of 22q11.2DS provides an attractive model to increase our understanding of the development and pathogenesis of schizophrenia and other psychiatric disorders in 22q11.2DS and in wider population.
有压倒性的证据表明,患有22q11.2缺失综合征(22q11.2DS)的儿童和成人具有特征性的行为表型。特别是,越来越多的证据表明22q11.2DS与精神分裂症之间存在明确的关联,尤其是在成年期。22q11.2缺失是精神分裂症发生的第三大风险因素,仅次于父母双方均患有精神分裂症的子女或患病个体的同卵双胞胎。对精神分裂症患者的连锁和关联研究都涉及了几个易感基因,其中三个位于22q11.2区域:儿茶酚-O-甲基转移酶(COMT)、脯氨酸脱氢酶(PRODH)和Gnb1L。此外,Gnb1L的变异与22q11.2DS男性患者的精神病症状有关。在22q11.2DS的小鼠模型中,Tbx1和Gnb1L的单倍剂量不足与前脉冲抑制降低有关,前脉冲抑制是一种精神分裂症的内表型。对22q11.2DS的研究为增进我们对22q11.2DS及更广泛人群中精神分裂症和其他精神障碍的发生发展及发病机制的理解提供了一个有吸引力的模型。