Imaging Genetics Center, Mark and Mary Stevens Neuroimaging & Informatics Institute, Keck School of Medicine of the University of Southern California, Marina del Rey, CA, USA.
Department of Child and Adolescent Psychiatry, Hospital General Universitario Gregorio Marañón, Universidad Complutense, School of Medicine, IiSGM, Madrid, Spain.
Mol Psychiatry. 2020 Nov;25(11):2818-2831. doi: 10.1038/s41380-019-0450-0. Epub 2019 Jul 29.
22q11.2 deletion syndrome (22q11DS)-a neurodevelopmental condition caused by a hemizygous deletion on chromosome 22-is associated with an elevated risk of psychosis and other developmental brain disorders. Prior single-site diffusion magnetic resonance imaging (dMRI) studies have reported altered white matter (WM) microstructure in 22q11DS, but small samples and variable methods have led to contradictory results. Here we present the largest study ever conducted of dMRI-derived measures of WM microstructure in 22q11DS (334 22q11.2 deletion carriers and 260 healthy age- and sex-matched controls; age range 6-52 years). Using harmonization protocols developed by the ENIGMA-DTI working group, we identified widespread reductions in mean, axial and radial diffusivities in 22q11DS, most pronounced in regions with major cortico-cortical and cortico-thalamic fibers: the corona radiata, corpus callosum, superior longitudinal fasciculus, posterior thalamic radiations, and sagittal stratum (Cohen's d's ranging from -0.9 to -1.3). Only the posterior limb of the internal capsule (IC), comprised primarily of corticofugal fibers, showed higher axial diffusivity in 22q11DS. 22q11DS patients showed higher mean fractional anisotropy (FA) in callosal and projection fibers (IC and corona radiata) relative to controls, but lower FA than controls in regions with predominantly association fibers. Psychotic illness in 22q11DS was associated with more substantial diffusivity reductions in multiple regions. Overall, these findings indicate large effects of the 22q11.2 deletion on WM microstructure, especially in major cortico-cortical connections. Taken together with findings from animal models, this pattern of abnormalities may reflect disrupted neurogenesis of projection neurons in outer cortical layers.
22q11.2 缺失综合征(22q11DS)-一种由染色体 22 上的杂合性缺失引起的神经发育疾病-与精神病和其他发育性脑疾病的风险增加有关。先前的单部位弥散磁共振成像(dMRI)研究报告了 22q11DS 中白质(WM)微观结构的改变,但由于样本量小和方法不同,导致结果相互矛盾。在这里,我们展示了迄今为止对 22q11DS 的 dMRI 衍生 WM 微观结构进行的最大研究(334 名 22q11.2 缺失携带者和 260 名健康的年龄和性别匹配的对照者;年龄范围为 6-52 岁)。使用 ENIGMA-DTI 工作组制定的协调协议,我们在 22q11DS 中发现了平均、轴向和径向扩散率的广泛降低,在主要的皮质-皮质和皮质-丘脑纤维区域最为明显:放射冠、胼胝体、上纵束、后丘脑辐射和矢状层(Cohen's d 从-0.9 到-1.3)。只有内囊后肢(IC),主要由皮质传出纤维组成,在 22q11DS 中表现出更高的轴向扩散率。22q11DS 患者在胼胝体和投射纤维(IC 和放射冠)中的平均分数各向异性(FA)高于对照组,但在以联合纤维为主的区域中 FA 低于对照组。22q11DS 中的精神病与多个区域的弥散率降低更为显著相关。总的来说,这些发现表明 22q11.2 缺失对 WM 微观结构有很大的影响,特别是在主要的皮质-皮质连接中。与动物模型的发现相结合,这种异常模式可能反映了外皮质层投射神经元的神经发生中断。