Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Schizophr Res. 2012 Oct;141(1):65-71. doi: 10.1016/j.schres.2012.07.015. Epub 2012 Aug 11.
Neuroanatomical and cognitive alterations typical of schizophrenia (SZ) patients are observed to a lesser extent in their adolescent and adult first-degree relatives, likely reflecting neurodevelopmental abnormalities associated with genetic risk for the illness. The anatomical pathways for language are hypothesized to be abnormal and to underlie the positive symptoms of schizophrenia. Examining non-psychotic relatives at high familial risk (FHR) for schizophrenia may clarify if these deficits represent trait markers associated with genetic vulnerability, rather than specific markers resulting from the pathological process underlying schizophrenia.
T1 MRI scans from a 3T Siemens scanner of young adult FHR subjects (N=46) and controls with no family history of illness (i.e. at low genetic risk LRC; N=31) were processed using FreeSurfer 5.0. We explored volumetric and lateralization alterations in regions associated with language processing. An extensive neuropsychological battery of language measures was administered.
No significant differences were observed between groups on any language measures. Controlling intracranial volume, significantly smaller left pars triangularis (PT) (p<0.01) and right pars orbitalis (PO) (p<0.01) volumes and reversal of the L>R pars orbitalis (p<0.001) lateralization were observed in FHR subjects. In addition, the L pars triangularis and R pars orbitalis correlated with performance on tests of linguistic function in the FHR group.
Reduced volume and reversed structural asymmetry in language-related regions hypothesized to be altered in SZ are also found in first degree relatives at FHR, despite normal language performance. To clarify if these findings are endophenotypes for Sz, future studies would need to be performed of ill and well family members no longer within the age range of risk for illness to show these deficits segregate with schizophrenia within families. Moreover, measures of complex language need to be studied to determine if FHR individuals manifest impairments in some aspects of language function.
精神分裂症(SZ)患者的神经解剖和认知改变在其青少年和成年一级亲属中观察到的程度较轻,这可能反映了与疾病遗传风险相关的神经发育异常。语言的解剖途径被假设为异常的,并构成精神分裂症阳性症状的基础。检查具有精神分裂症高家族风险(FHR)的非精神病亲属,可以阐明这些缺陷是否代表与遗传易感性相关的特征标志物,而不是精神分裂症潜在病理过程的特定标志物。
使用 FreeSurfer 5.0 处理来自年轻成年 FHR 受试者(N=46)和无疾病家族史(即低遗传风险 LRC;N=31)的 3T 西门子扫描仪的 T1 MRI 扫描。我们探索了与语言处理相关的区域的体积和侧化改变。进行了广泛的语言神经心理学测试。
在任何语言测试中,两组之间均未观察到显著差异。在 FHR 受试者中,控制颅内体积后,左侧三角部(PT)(p<0.01)和右侧眶部(PO)(p<0.01)体积以及右侧眶部(PO)的 L>R 侧化逆转显著较小(p<0.001)。此外,在 FHR 组中,L 三角部和 R 眶部与语言功能测试的表现相关。
在 FHR 的一级亲属中,也发现了与 SZ 改变的语言相关区域的体积减小和结构不对称性逆转,尽管语言表现正常。为了阐明这些发现是否是 Sz 的内表型,需要对不再处于发病风险年龄段的患病和未患病的家庭成员进行进一步研究,以显示这些缺陷在家庭内与精神分裂症一起分离。此外,需要研究复杂语言的衡量标准,以确定 FHR 个体是否在某些语言功能方面表现出缺陷。