Liu Kai, Zhang Teng, Zhang Qing, Sun Yueji, Wu Jianlin, Lei Yi, Chu Winnie C W, Mok Vincent C T, Wang Defeng, Shi Lin
Department of Imaging and Interventional Radiology, The Chinese University of Hong Kong Hong Kong, China.
Department of Radiology, Affiliated Zhongshan Hospital of Dalian University Dalian, China.
Front Psychol. 2016 May 30;7:809. doi: 10.3389/fpsyg.2016.00809. eCollection 2016.
Schizotypal personality disorder (SPD) is considered one of the classic disconnection syndromes. However, the specific cortical disconnectivity pattern has not been fully investigated. In this study, we aimed to explore significant alterations in whole-cortex structural connectivity in SPD individuals (SPDs) by combining the techniques of brain surface morphometry and white matter tractography. Diffusion and structural MR data were collected from 20 subjects with SPD (all males; age, 19.7 ± 0.9 years) and 18 healthy controls (all males; age, 20.3 ± 1.0 years). To measure the structural connectivity for a given unit area of the cortex, the fiber connectivity density (FiCD) value was proposed and calculated as the sum of the fractional anisotropy of all the fibers connecting to that unit area in tractography. Then, the resultant whole-cortex FiCD maps were compared in a vertex-wise manner between SPDs and controls. Compared with normal controls, SPDs showed significantly decreased FiCD in the rostral middle frontal gyrus (crossing BA 9 and BA 10) and significantly increased FiCD in the anterior part of the fusiform/inferior temporal cortex (P < 0.05, Monte Carlo simulation corrected). Moreover, the gray matter volume extracted from the left rostral middle frontal cluster was observed to be significantly greater in the SPD group (P = 0.02). Overall, this study identifies a decrease in connectivity in the left middle frontal cortex as a key neural deficit at the whole-cortex level in SPD, thus providing insight into its neuropathological basis.
分裂型人格障碍(SPD)被认为是典型的神经连接障碍综合征之一。然而,具体的皮质连接障碍模式尚未得到充分研究。在本研究中,我们旨在通过结合脑表面形态测量技术和白质纤维束成像技术,探索SPD个体(SPDs)全脑皮质结构连接的显著改变。我们收集了20名SPD患者(均为男性;年龄19.7±0.9岁)和18名健康对照者(均为男性;年龄20.3±1.0岁)的扩散加权和结构磁共振数据。为了测量皮质给定单位面积的结构连接性,我们提出并计算了纤维连接密度(FiCD)值,其计算方法为纤维束成像中连接到该单位面积的所有纤维的各向异性分数之和。然后,以顶点为单位,比较了SPDs和对照组的全脑FiCD图。与正常对照组相比,SPDs在额中回前部(跨越BA 9和BA 10)的FiCD显著降低,在梭状回/颞下回前部的FiCD显著升高(P<0.05,经蒙特卡洛模拟校正)。此外,在SPD组中,从左侧额中回前部簇提取的灰质体积显著更大(P = 0.02)。总体而言,本研究确定左侧额中回皮质连接性降低是SPD全脑水平的关键神经缺陷,从而为其神经病理学基础提供了见解。