Seidman Larry J, Pantelis Christos, Keshavan Matcheri S, Faraone Stephen V, Goldstein Jill M, Horton Nicholas J, Makris Nikos, Falkai Peter, Caviness Verne S, Tsuang Ming T
Commonwealth Research Center, Harvard Medical School, Department of Psychiatry, Massachusetts Mental Health Center, Boston, MA, USA.
Schizophr Bull. 2003;29(4):803-30. doi: 10.1093/oxfordjournals.schbul.a007048.
A central question in schizophrenia research is which brain abnormalities are independent of psychosis and which evolve before and after psychosis begins. This question can be addressed by longitudinal neuroimaging studies beginning in the prodrome, but at present there is only one published study. We reviewed the literature on structural brain imaging in persons with chronic and first episode schizophrenia, nonpsychotic persons at genetic high risk, and persons thought to be at risk for imminent psychosis ("prodromal" persons). Medial temporal lobe (MTL), especially hippocampal, volume alterations are among the most robust brain vulnerabilities for schizophrenia. Because verbal declarative memory (VDM) deficits are prominent and the parahippocampal gyrus (PHG) is considered to be centrally involved with the hippocampus in VDM processing, we analyzed PHG data from a family study of schizophrenia. Patients with schizophrenia and nonpsychotic relatives from "multiplex" families (families with multiple persons with schizophrenia) had significantly smaller right parahippocampal anterior (PHa) volumes than controls. Marginally significant findings were observed for the left PHa. Unexpectedly, relatives from "simplex" families (families with only one person with schizophrenia) had significantly larger PH posterior volumes than controls and did not differ from controls on PHa. Results provide some support for the hypothesis that the vulnerability to schizophrenia includes abnormal volumes of the PHG. These data provide additional support for the hypothesis that some MTL abnormalities in schizophrenia are independent of psychosis, at least in families with presumably high genetic loading. Implications of genetic risk studies for prodromal research are discussed.
精神分裂症研究中的一个核心问题是,哪些大脑异常与精神病无关,以及哪些在精神病发作之前和之后出现。这个问题可以通过从前驱期开始的纵向神经影像学研究来解决,但目前只有一项已发表的研究。我们回顾了关于慢性和首发精神分裂症患者、遗传高危的非精神病患者以及被认为有即将发生精神病风险的人群(“前驱期”人群)的脑结构成像的文献。内侧颞叶(MTL),尤其是海马体的体积改变,是精神分裂症最明显的大脑易损特征之一。由于言语陈述性记忆(VDM)缺陷很突出,且海马旁回(PHG)被认为在VDM处理过程中与海马体密切相关,我们分析了一项精神分裂症家族研究中的PHG数据。来自“多重”家庭(有多名精神分裂症患者的家庭)的精神分裂症患者和非精神病亲属的右侧海马旁回前部(PHa)体积明显小于对照组。左侧PHa有边缘性显著结果。出乎意料的是,来自“单重”家庭(只有一名精神分裂症患者的家庭)的亲属的PH后部体积明显大于对照组,且在PHa上与对照组没有差异。结果为精神分裂症易感性包括PHG体积异常这一假设提供了一些支持。这些数据为精神分裂症中一些MTL异常与精神病无关这一假设提供了额外支持,至少在可能具有高遗传负荷的家庭中是如此。讨论了遗传风险研究对前驱期研究的意义。