Developmental Imaging and Psychopathology Laboratory, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
Developmental Imaging and Psychopathology Laboratory, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
Schizophr Res. 2017 Oct;188:52-58. doi: 10.1016/j.schres.2017.01.031. Epub 2017 Jan 27.
Approximately 30% of individuals with 22q11.2 Deletion Syndrome (22q11DS) develop schizophrenia during adolescence/early adulthood, making this syndrome a model for the disorder. Furthermore, negative symptoms exist in up to 80% of patients diagnosed with 22q11DS. The present study aims to uncover morphological brain alterations associated with negative symptoms in a cohort of patients with 22q11DS who are at-risk for developing schizophrenia. A total of 71 patients with 22q11DS aged 12 to 35 (54% females) with no past or present diagnosis of a schizophrenia were included in the study. Psychotic symptom scores were used to divide patients into subgroups by means of a cluster analysis. Three major subgroups were evident: patients with low negative and positive symptoms; patients with high negative symptoms and low positive symptoms; and patients with high negative and positive symptoms. Cortical volume, thickness and gyrification were compared between subgroups using FreeSurfer software. Results showed that patients with high negative symptoms, compared to those with low negative symptoms, have decreased gyrification in the medial occipito-temporal (MOT) and lateral temporo-parietal (LTP) cortices of the left hemisphere, and in the medial temporal (MT)/posterior cingulate (PCC) cortices of the right hemisphere. These findings suggest that high negative symptoms are associated with gyrification reductions predominantly in medial occipital and temporal regions, which are areas implicated in social cognition and early visual processing. Furthermore, as cortical folding develops in utero and during the first years of life, reduced gyrification may represent an early biomarker predicting the development of negative symptoms.
约 30%的 22q11.2 缺失综合征(22q11DS)患者在青少年/成年早期发展为精神分裂症,使该综合征成为该疾病的模型。此外,80%被诊断为 22q11DS 的患者存在阴性症状。本研究旨在揭示与 22q11DS 患者阴性症状相关的形态学脑改变,这些患者有发展为精神分裂症的风险。共有 71 名年龄在 12 至 35 岁之间(54%为女性)的 22q11DS 患者(无过去或现在的精神分裂症诊断)纳入研究。使用精神病症状评分通过聚类分析将患者分为亚组。有三个主要的亚组:阴性和阳性症状低的患者;阴性症状高而阳性症状低的患者;阴性和阳性症状高的患者。使用 FreeSurfer 软件比较了亚组之间的皮质体积、厚度和脑回。结果表明,与阴性症状低的患者相比,阴性症状高的患者左侧大脑中颞叶(MOT)和外侧颞顶叶(LTP)皮质以及右侧大脑中颞叶(MT)/后扣带回(PCC)皮质的脑回减少。这些发现表明,高阴性症状与主要在中颞和中颞区域的脑回减少有关,这些区域与社会认知和早期视觉处理有关。此外,由于皮质折叠在子宫内和生命的头几年发育,脑回减少可能代表预测阴性症状发展的早期生物标志物。