Suo Xueling, Pan Nanfang, Chen Li, Li Lingjiang, Kemp Graham J, Wang Song, Gong Qiyong
Department of Radiology, Huaxi MR Research Center (HMRRC), Institution of Radiology and Medical Imaging, West China Hospital of Sichuan University, Chengdu 610041, Sichuan, China.
Functional and Molecular lmaging Key Laboratory of Sichuan Province, West China Hospital of Sichuan University, Chengdu 610041, Sichuan, China.
Depress Anxiety. 2024 Nov 1;2024:4399757. doi: 10.1155/2024/4399757. eCollection 2024.
The heterogeneity of posttraumatic stress disorder (PTSD) is an obstacle to both understanding and therapy, and this has prompted a search for internally homogeneous neuroradiological subgroups within the broad clinical diagnosis. We set out to do this using the individual differential structural covariance network (IDSCN). We constructed cortical thickness-based IDSCN using T1-weighted images of 89 individuals with PTSD (mean age 42.8 years, 60 female) and 89 demographically matched trauma-exposed non-PTSD (TENP) controls (mean age 43.1 years, 63 female). The IDSCN metric quantifies how the structural covariance edges in a patient differ from those in the controls. We examined the structural diversity of PTSD and variation among subtypes using a hierarchical clustering analysis. PTSD patients exhibited notable diversity in distinct structural covariance edges but mainly affecting three networks: default mode, ventral attention, and sensorimotor. These changes predicted individual PTSD symptom severity. We identified two neuroanatomical subtypes: the one with higher PTSD symptom severity showed lower structural covariance edges in the frontal cortex and between frontal, parietal, and occipital cortex-regions that are functionally implicated in selective attention, response selection, and learning tasks. Thus, deviations in structural covariance in large-scale networks are common in PTSD but fall into two subtypes. This work sheds light on the neurobiological mechanisms underlying the clinical heterogeneity and may aid in personalized diagnosis and therapeutic interventions.
创伤后应激障碍(PTSD)的异质性是理解和治疗该疾病的障碍,这促使人们在广泛的临床诊断中寻找内部同质的神经放射学子组。我们使用个体差异结构协方差网络(IDSCN)来进行这项研究。我们使用89名PTSD患者(平均年龄42.8岁,60名女性)和89名人口统计学匹配的创伤暴露非PTSD(TENP)对照者(平均年龄43.1岁,63名女性)的T1加权图像构建基于皮质厚度的IDSCN。IDSCN指标量化了患者的结构协方差边与对照者的结构协方差边之间的差异。我们使用层次聚类分析检查了PTSD的结构多样性和亚型间的差异。PTSD患者在不同的结构协方差边表现出显著的多样性,但主要影响三个网络:默认模式网络、腹侧注意网络和感觉运动网络。这些变化预测了个体PTSD症状的严重程度。我们识别出两种神经解剖学亚型:PTSD症状严重程度较高的亚型在额叶皮质以及额叶、顶叶和枕叶皮质之间显示出较低的结构协方差边,这些区域在选择性注意、反应选择和学习任务中具有功能牵连。因此,大规模网络中结构协方差的偏差在PTSD中很常见,但可分为两种亚型。这项工作揭示了临床异质性背后的神经生物学机制,并可能有助于个性化诊断和治疗干预。