Network Centrality and Modularity of Structural Covariance Networks in Posttraumatic Stress Disorder: A Multisite ENIGMA-PGC Study.

IF 2.4 3区 医学 Q3 NEUROSCIENCES Brain connectivity Pub Date : 2023-05-01 Epub Date: 2023-02-09 DOI:10.1089/brain.2022.0038
Gopalkumar Rakesh, Mark W Logue, Emily Clarke-Rubright, Courtney C Haswell, Paul M Thompson, Michael D De Bellis, Rajendra A Morey, Delin Sun
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Abstract

Introduction: Cortical thickness (CT) and surface area (SA) are established biomarkers of brain pathology in posttraumatic stress disorder (PTSD). Structural covariance networks (SCNs) are represented as graphs with brain regions as nodes and correlations between nodes as edges. Methods: We built SCNs for PTSD and control groups using 148 CT and SA measures that were harmonized for site in n = 3439 subjects from Enhancing Neuroimaging Genetics through Meta-Analysis (ENIGMA)-Psychiatric Genomics Consortium (PGC) PTSD. We compared centrality between PTSD and controls as well as interactions of diagnostic group with age, sex, and comorbid major depressive disorder (MDD) status. We investigated associations between network modularity and diagnostic grouping. Results: Nodes with higher CT-based centrality in PTSD compared with controls included the left inferior frontal sulcus, left fusiform gyrus, left superior temporal gyrus, and right inferior temporal gyrus. Children (<10 years) and adolescents (10-21) with PTSD showed greater centrality in frontotemporal areas compared with young (22-39) and middle-aged adults (40-59) with PTSD, who showed higher centrality in occipital areas. The PTSD diagnostic group interactions with sex and comorbid MDD showed altered centrality in occipital regions, along with greater visual network (VN) modularity in PTSD subjects compared with controls. Conclusion: Structural covariance in PTSD is associated with centrality differences in occipital areas and VN modularity differences in a large well-powered sample. In the context of extensive structural covariance remodeling taking place before and during adolescence, the present findings suggest a process of cortical remodeling that commences with trauma and/or the onset of PTSD but may also predate these events. Impact statement Centrality is a graph theory measure that offers insights into a node's relationship with all other nodes in the brain. Centrality pinpoints the drivers of brain communication within networks and nodes and may be a promising target for treatments such as neuromodulation. Modularity can pinpoint modules that exist within larger networks and quantify the connections between these modules. Centrality and modularity complement functional and structural connectivity measurements within specific brain networks.

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创伤后应激障碍中结构协方差网络的网络中心性和模块性:多站点 ENIGMA-PGC 研究》。
简介皮层厚度(CT)和表面积(SA)是创伤后应激障碍(PTSD)脑部病理的既定生物标志物。结构协方差网络(SCN)是以大脑区域为节点、节点之间的相关性为边缘的图。研究方法我们使用 148 项 CT 和 SA 测量建立了创伤后应激障碍组和对照组的结构协方差网络(SCNs),这些测量对来自增强神经影像遗传学元分析(ENIGMA)- 精神病基因组学联合会(PGC)创伤后应激障碍研究的 n = 3439 名受试者的部位进行了协调。我们比较了创伤后应激障碍和对照组之间的中心性,以及诊断组与年龄、性别和合并重度抑郁障碍 (MDD) 状态的交互作用。我们还研究了网络模块化与诊断分组之间的关联。结果发现与对照组相比,创伤后应激障碍患者的CT中心性更高的节点包括左额下沟、左蝶回、左颞上回和右颞下回。儿童(结论:创伤后应激障碍的结构协方差与枕叶区的中心性差异和VN模块化差异有关。在青春期前和青春期发生广泛的结构协方差重塑的背景下,本研究结果表明,皮质重塑过程始于创伤和/或创伤后应激障碍的发病,但也可能早于这些事件。影响声明 中心性是一种图论测量方法,可帮助人们深入了解一个节点与大脑中所有其他节点的关系。中心性可以确定网络和节点内大脑交流的驱动因素,可能是神经调节等治疗方法的一个有前途的目标。模块性可以精确定位存在于更大网络中的模块,并量化这些模块之间的联系。中心性和模块性是对特定大脑网络内功能和结构连通性测量的补充。
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来源期刊
Brain connectivity
Brain connectivity Neuroscience-General Neuroscience
CiteScore
4.80
自引率
0.00%
发文量
80
期刊介绍: Brain Connectivity provides groundbreaking findings in the rapidly advancing field of connectivity research at the systems and network levels. The Journal disseminates information on brain mapping, modeling, novel research techniques, new imaging modalities, preclinical animal studies, and the translation of research discoveries from the laboratory to the clinic. This essential journal fosters the application of basic biological discoveries and contributes to the development of novel diagnostic and therapeutic interventions to recognize and treat a broad range of neurodegenerative and psychiatric disorders such as: Alzheimer’s disease, attention-deficit hyperactivity disorder, posttraumatic stress disorder, epilepsy, traumatic brain injury, stroke, dementia, and depression.
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