Nenadic Igor, Dietzek Maren, Schönfeld Nils, Lorenz Carsten, Gussew Alexander, Reichenbach Jürgen R, Sauer Heinrich, Gaser Christian, Smesny Stefan
Department of Psychiatry and Psychotherapy, Jena University Hospital, 07743 Jena, Germany.
Department of Psychiatry and Psychotherapy, Jena University Hospital, 07743 Jena, Germany.
Schizophr Res. 2015 Feb;161(2-3):169-76. doi: 10.1016/j.schres.2014.10.041. Epub 2014 Dec 12.
Early intervention research in schizophrenia has suggested that brain structural alterations might be present in subjects at high risk of developing psychosis. The heterogeneity of regional effects of these changes, which is established in schizophrenia, however, has not been explored in prodromal or high-risk populations. We used high-resolution MRI and voxel-based morphometry (VBM8) to analyze grey matter differences in 43 ultra high-risk subjects for psychosis (meeting ARMS criteria, identified through CAARMS interviews), 24 antipsychotic-naïve first-episode schizophrenia patients and 49 healthy controls (groups matched for age and gender). Compared to healthy controls, resp., first-episode schizophrenia patients had reduced regional grey matter in left prefrontal, insula, right parietal and left temporal cortices, while the high-risk group showed reductions in right middle temporal and left anterior frontal cortices. When dividing the ultra-high-risk group in those with a genetic risk vs. those with attenuated psychotic symptoms, the former showed left anterior frontal, right caudate, as well as a smaller right hippocampus, and amygdala reduction, while the latter subgroup showed right middle temporal cortical reductions (each compared to healthy controls). Our findings in a clinical psychosis high-risk cohort demonstrate variability of brain structural changes according to subgroup and background of elevated risk, suggesting frontal and possibly also hippocampal/amygdala changes in individuals with genetic susceptibility. Heterogeneity of structural brain changes (as seen in schizophrenia) appears evident even at high-risk stage, prior to potential onset of psychosis.
精神分裂症的早期干预研究表明,在有发展为精神病高风险的受试者中可能存在脑结构改变。然而,这些变化在精神分裂症中已得到证实的区域效应异质性,尚未在前驱期或高风险人群中进行探索。我们使用高分辨率MRI和基于体素的形态测量法(VBM8)来分析43名精神病超高风险受试者(符合ARMS标准,通过CAARMS访谈确定)、24名未使用过抗精神病药物的首发精神分裂症患者和49名健康对照者(年龄和性别匹配组)的灰质差异。与健康对照者相比,首发精神分裂症患者左侧前额叶、脑岛、右侧顶叶和左侧颞叶皮质的区域灰质减少,而高风险组右侧颞中回和左侧前额叶皮质减少。当将超高风险组分为有遗传风险者和有精神病性症状减弱者时,前者表现为左侧前额叶、右侧尾状核以及右侧海马体较小,杏仁核缩小,而后者亚组表现为右侧颞中回皮质减少(均与健康对照者相比)。我们在临床精神病高风险队列中的研究结果表明,根据亚组和风险升高背景,脑结构变化存在变异性,提示有遗传易感性的个体存在额叶以及可能还有海马体/杏仁核的变化。即使在精神病可能发作之前的高风险阶段,脑结构变化的异质性(如在精神分裂症中所见)似乎也很明显。