Regional cortical thinning in subjects with high genetic loading for schizophrenia

被引:37
作者
Byun, Min Soo [1 ]
Kim, June Sic [2 ]
Jung, Wi Hoon [3 ]
Jang, Joon Hwan [1 ]
Choi, Jung-Seok [1 ]
Kim, Sung Nyun [1 ]
Choi, Chi-Hoon [4 ]
Chung, Chun Kee [2 ]
An, Suk Kyoon [5 ]
Kwon, Jun Soo [1 ,3 ,6 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Psychiat, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Neurosurg, MEG Ctr, Seoul 110744, South Korea
[3] SNU MRC, Inst Human Behav Med, Seoul, South Korea
[4] Natl Med Ctr, Dept Diagnost Radiol, Seoul, South Korea
[5] Yonsei Univ, Coll Med, Dept Psychiat, Seoul, South Korea
[6] Seoul Natl Univ, Coll Nat Sci, World Class Univ Program, Dept Brain & Cognit Sci, Seoul 110744, South Korea
关键词
Schizophrenia; Genetic high risk; Cortical thickness; Genetic liability; Endophenotype; DORSOLATERAL PREFRONTAL CORTEX; 1ST EPISODE SCHIZOPHRENIA; VOXEL-BASED MORPHOMETRY; HIGH-RISK; GRAY-MATTER; CEREBRAL-CORTEX; YOUNG-ADULTS; VULNERABILITY INDICATOR; 1ST-DEGREE RELATIVES; BRAIN STRUCTURE;
D O I
10.1016/j.schres.2012.08.028
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Although recent studies have revealed regional cortical thinning in patients with schizophrenia, it is not clear whether cortical thinning reflects a genetic liability for schizophrenia. The present study investigated the change of cortical thickness in subjects at genetic high risk (GHR) for schizophrenia with a relatively high genetic loading compared with healthy controls (HC) and patients with schizophrenia. The effect of genetic loading on cortical thinning was also measured by comparing GHR subgroups according to the levels of genetic loading. Methods: Cortical thickness was measured by the Constrained Laplacian-based Automated Segmentation with Proximities algorithm using 1.5-T structural MRI scans. The cortical thickness of the subjects at GHR (n = 31) was compared with that of HC (n = 29) and patients with schizophrenia (n = 31). We then compared the cortical thickness of the GHR subgroups according to the number of first-degree relatives with schizophrenia to measure the effect of genetic loading. Results: Relative to HC, GHR subjects showed significant cortical thinning in the right anterior cingulate cortex (ACC), left paracingulate and posterior cingulate regions; bilateral frontal regions including frontal pole and ventromedial prefrontal cortex; bilateral temporal regions including the left parahippocampal gyrus; and bilateral inferior parietal and occipital regions; however, patients with schizophrenia showed more widespread cortical thinning in the fronto-temporo-parietal region. GHR subjects who had two or more first-degree relatives with schizophrenia showed a greater reduction in cortical thickness in the right ACC and in the left paracingulate cortex than did those who had only one first-degree relative with schizophrenia. Conclusion: Our findings suggest that the level of genetic loading may have a dose-dependent effect on cortical thinning in the right ACC and in the left paracingulate cortex and that cortical thinning in GHR subjects may represent neurodevelopmental alterations that result from genetic liability for schizophrenia. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:197 / 203
页数:7
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