Goldman Aaron L, Pezawas Lukas, Mattay Venkata S, Fischl Bruce, Verchinski Beth A, Chen Qiang, Weinberger Daniel R, Meyer-Lindenberg Andreas
Neuroimaging Core Facility, Genes, Cognition, and Psychosis Program, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892, USA.
Arch Gen Psychiatry. 2009 May;66(5):467-77. doi: 10.1001/archgenpsychiatry.2009.24.
Schizophrenia is a brain disorder with predominantly genetic risk factors, and previous research has identified heritable cortical and subcortical reductions in local brain volume. To our knowledge, cortical thickness, a measure of particular interest in schizophrenia, has not previously been evaluated in terms of its heritability in relationship to risk for schizophrenia.
To quantify the distribution and heritability of cortical thickness changes in schizophrenia.
We analyzed a large sample of normal controls, affected patients, and unaffected siblings using a surface-based approach. Cortical thickness was compared between diagnosis groups on a surfacewide node-by-node basis. Heritability related to disease risk was assessed in regions derived from an automated cortical parcellation algorithm by calculating the Risch lambda.
Research hospital.
One hundred ninety-six normal controls, 115 affected patients with schizophrenia, and 192 unaffected siblings.
Regional cortical thickness.
Node-by-node mapping statistics revealed widespread thickness reductions in the patient group, most pronouncedly in the frontal lobe and temporal cortex. Unaffected siblings did not significantly differ from normal controls at the chosen conservative threshold. Risch lambda analysis revealed widespread evidence for heritability for cortical thickness reductions throughout the brain.
To our knowledge, the present study provides the first evidence of broadly distributed and heritable reductions of cortical thickness alterations in schizophrenia. However, since only trend-level reductions of thickness were observed in siblings, cortical thickness per se (at least as measured by this approach) is not a strong intermediate phenotype for schizophrenia.
精神分裂症是一种主要由遗传风险因素导致的脑部疾病,先前的研究已发现大脑局部体积在皮层和皮层下存在可遗传的减少。据我们所知,皮层厚度是精神分裂症研究中特别受关注的一个指标,但此前尚未就其与精神分裂症风险的关系进行遗传性评估。
量化精神分裂症患者皮层厚度变化的分布及遗传性。
我们采用基于表面的方法分析了大量正常对照者、患病患者及未患病同胞的数据。在全脑表面逐节点比较诊断组之间的皮层厚度。通过计算里施λ值,在自动皮层分区算法得出的区域中评估与疾病风险相关的遗传性。
研究医院。
196名正常对照者、115名患有精神分裂症的患者及192名未患病同胞。
区域皮层厚度。
逐节点映射统计显示,患者组皮层厚度普遍降低,最明显的是额叶和颞叶皮层。在选定的保守阈值下,未患病同胞与正常对照者无显著差异。里施λ分析显示,全脑皮层厚度降低具有广泛的遗传性证据。
据我们所知,本研究首次提供了精神分裂症患者皮层厚度改变广泛分布且具有遗传性的证据。然而,由于在同胞中仅观察到厚度呈趋势性降低,皮层厚度本身(至少以此方法测量)并非精神分裂症的强中间表型。