Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Harvard Medical School, Brigham and Women's Hospital, 1249 Boylston St, Boston, MA, 02215, USA.
Department of Child and Adolescent Psychiatry, Psychosomatic and Psychotherapy, Ludwig- Maximilians- Universität, Munich, Germany.
Brain Imaging Behav. 2018 Feb;12(1):54-63. doi: 10.1007/s11682-016-9666-7.
Neuroimaging studies demonstrate gray matter (GM) macrostructural abnormalities in patients with schizophrenia (SCZ). While ex-vivo and genetic studies suggest cellular pathology associated with abnormal neurodevelopmental processes in SCZ, few in-vivo measures have been proposed to target microstructural GM organization. Here, we use diffusion heterogeneity- to study GM microstructure in SCZ. Structural and diffusion magnetic resonance imaging (MRI) were acquired on a 3 Tesla scanner in 46 patients with SCZ and 37 matched healthy controls (HC). After correction for free water, diffusion heterogeneity as well as commonly used diffusion measures FA and MD and volume were calculated for the four cortical lobes on each hemisphere, and compared between groups. Patients with early course SCZ exhibited higher diffusion heterogeneity in the GM of the frontal lobes compared to controls. Diffusion heterogeneity of the frontal lobe showed excellent discrimination between patients and HC, while none of the commonly used diffusion measures such as FA or MD did. Higher diffusion heterogeneity in the frontal lobes in early SCZ may be due to abnormal brain maturation (migration, pruning) before and during adolescence and early adulthood. Further studies are needed to investigate the role of heterogeneity as potential biomarker for SCZ risk.
神经影像学研究表明精神分裂症(SCZ)患者存在灰质(GM)宏观结构异常。虽然离体和遗传研究表明与 SCZ 异常神经发育过程相关的细胞病理学,但很少有针对 GM 微观结构组织的体内测量方法。在这里,我们使用扩散异质性来研究 SCZ 的 GM 微观结构。在 3T 扫描仪上对 46 名 SCZ 患者和 37 名匹配的健康对照(HC)进行了结构和扩散磁共振成像(MRI)扫描。在对游离水进行校正后,计算了每个半球四个皮质叶的扩散异质性以及常用的扩散测量值 FA 和 MD 和体积,并在组间进行了比较。与对照组相比,早期 SCZ 患者的额叶 GM 中扩散异质性更高。额叶的扩散异质性可以很好地区分患者和 HC,而常用的扩散测量值如 FA 或 MD 则不行。早期 SCZ 患者额叶的扩散异质性较高可能是由于青春期前和青春期期间大脑成熟(迁移、修剪)异常所致。需要进一步的研究来探讨异质性作为 SCZ 风险的潜在生物标志物的作用。