Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States; Department of Psychiatry and Psychotherapy, Jena University Hospital, Germany; Department of Clinical Psychology, Friedrich-Schiller-University Jena, Am Steiger 3, Haus 1, Jena 07743, Germany.
Department of Clinical Psychology, Friedrich-Schiller-University Jena, Am Steiger 3, Haus 1, Jena 07743, Germany.
Psychiatry Res. 2021 Jul;301:113979. doi: 10.1016/j.psychres.2021.113979. Epub 2021 May 3.
The 22q11.2 deletion syndrome (22q11DS) is a developmental genetic syndrome associated with a 30% risk for developing schizophrenia. Lateral ventricles and subcortical structures are abnormal in this syndrome as well as in schizophrenia. Here, we investigated whether these structures are related in young adults with 22q11DS with and without prodromal symptoms (PS) for schizophrenia and whether abnormalities in volumes are associated with global functioning. MR images were acquired on a 3T scanner from 51 individuals with 22q11DS and 30 healthy controls (mean age: 21±2 years). Correlations were performed to evaluate the relationship between ventricular and subcortical volumes, with Global Assessment of Functioning (GAF) and Premorbid Adjustment Scale (PAS) in each group. Lateral ventricular volumes correlated negatively with subcortical volumes in individuals with 22q11DS. In individuals with 22q11DS with PS only, GAF correlated positively with volumes of the lateral ventricles and negatively with subcortical volumes. PAS correlated negatively with lateral ventricle volumes, and positively with volumes of subcortical structures. The results suggest a common neurodevelopmental mechanism related to the growth of these brain structures. Further, the ratio between the volumes and clinical measures could potentially be used to characterize individuals with 22q11DS and those from the general population for the risk of the development of schizophrenia.
22q11.2 缺失综合征(22q11DS)是一种与精神分裂症发展风险 30%相关的发育性遗传综合征。该综合征以及精神分裂症中侧脑室和皮质下结构均异常。在这里,我们研究了有无精神分裂症前驱症状(PS)的年轻 22q11DS 患者中这些结构是否相关,以及体积异常是否与整体功能相关。在 3T 扫描仪上对 51 名 22q11DS 患者和 30 名健康对照者(平均年龄:21±2 岁)进行了 MRI 采集。在每个组中,进行相关性分析以评估脑室和皮质下体积与全球功能评估(GAF)和前驱期适应量表(PAS)之间的关系。22q11DS 患者中,侧脑室体积与皮质下体积呈负相关。仅在 22q11DS 患者中存在 PS 的情况下,GAF 与侧脑室体积呈正相关,与皮质下体积呈负相关。PAS 与侧脑室体积呈负相关,与皮质下结构体积呈正相关。结果表明,存在与这些脑结构生长相关的共同神经发育机制。此外,体积与临床测量的比值可能可用于对 22q11DS 患者和一般人群进行精神分裂症发病风险的特征化。