Xu Can-Xin, Kong Linghan, Jiang Hong, Jiang Yue, Sun Yu-Hao, Bian Liu-Guan, Feng Yuan, Sun Qing-Fang
Department of Neurosurgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Heliyon. 2024 Apr 3;10(7):e28957. doi: 10.1016/j.heliyon.2024.e28957. eCollection 2024 Apr 15.
Cushing disease (CD) is a rare clinical neuroendocrine disease. CD is characterized by abnormal hypercortisolism induced by a pituitary adenoma with the secretion of adrenocorticotropic hormone. Individuals with CD usually exhibit atrophy of gray matter volume. However, little is known about the alterations in topographical organization of individuals with CD. This study aimed to investigate the structural covariance networks of individuals with CD based on the gray matter volume using graph theory analysis.
High-resolution T1-weighted images of 61 individuals with CD and 53 healthy controls were obtained. Gray matter volume was estimated and the structural covariance network was analyzed using graph theory. Network properties such as hubs of all participants were calculated based on degree centrality.
No significant differences were observed between individuals with CD and healthy controls in terms of age, gender, and education level. The small-world features were conserved in individuals with CD but were higher than those in healthy controls. The individuals with CD showed higher global efficiency and modularity, suggesting higher integration and segregation as compared to healthy controls. The hub nodes of the individuals with CD were Short insular gyri (G_insular_short_L), Anterior part of the cingulate gyrus and sulcus (G_and_S_cingul-Ant_R), and Superior frontal gyrus (G_front_sup_R).
Significant differences in the structural covariance network of patients with CD were found based on graph theory. These findings might help understanding the pathogenesis of individuals with CD and provide insight into the pathogenesis of this CD.
库欣病(CD)是一种罕见的临床神经内分泌疾病。CD的特征是垂体腺瘤导致促肾上腺皮质激素分泌异常,引起皮质醇增多症。患有CD的个体通常表现出灰质体积萎缩。然而,对于CD患者大脑拓扑组织的改变知之甚少。本研究旨在基于灰质体积,运用图论分析方法研究CD患者的结构协方差网络。
获取了61例CD患者和53名健康对照者的高分辨率T1加权图像。估计灰质体积,并使用图论分析结构协方差网络。基于度中心性计算所有参与者的网络属性,如枢纽。
CD患者与健康对照者在年龄、性别和教育水平方面未观察到显著差异。CD患者保留了小世界特征,但高于健康对照者。CD患者表现出更高的全局效率和模块化程度,表明与健康对照者相比,其整合性和分离性更高。CD患者的枢纽节点为短岛叶回(G_insular_short_L)、扣带回和沟前部(G_and_S_cingul-Ant_R)以及额上回(G_front_sup_R)。
基于图论发现CD患者的结构协方差网络存在显著差异。这些发现可能有助于理解CD患者的发病机制,并为这种疾病的发病机制提供见解。