Relationship between intrinsic network connectivity and psychiatric symptom severity in functional seizures

默认模式网络 精神病理学 创伤性脑损伤 静息状态功能磁共振成像 心理学 焦虑 心情 连接体 精神科 脑岛 医学 临床心理学 神经科学 功能连接
作者
Adam M. Goodman,Pranav Kakulamarri,Rodolphe Nenert,Jane B. Allendorfer,Noah S. Philip,Stephen Correia,W. Curt LaFrance,Jerzy P. Szaflarski
出处
期刊:Journal of Neurology, Neurosurgery, and Psychiatry [BMJ]
卷期号:94 (2): 136-143 被引量:9
标识
DOI:10.1136/jnnp-2022-329838
摘要

Background Traumatic brain injury (TBI) may precipitate the onset of functional seizures (FSs). Many patients with FS report at least one prior TBI, and these patients typically present with more severe psychiatric comorbidities. TBI and psychopathology are linked to changes in neural network connectivity, but their combined effects on these networks and relationship to the effects of FS remain unclear. We hypothesised that resting-state functional connectivity (rsFC) would differ between patients with FS and TBI (FS+TBI) compared with TBI without FS (TBI only), with variability only partially explained by the presence of psychopathology. Methods Patients with FS+TBI (n=52) and TBI only (n=54) were matched for age and sex. All participants completed psychiatric assessments prior to resting-state functional MRI at 3 T. Independent component analysis identified five canonical rsFC networks related to emotion and motor functions. Results Five linear mixed-effects analyses identified clusters of connectivity coefficients that differed between groups within the posterior cingulate of the default mode network, insula and supramarginal gyrus of the executive control network and bilateral anterior cingulate of the salience network (all α=0.05, corrected). Cluster signal extractions revealed decreased contributions to each network for FS+TBI compared to TBI only. Planned secondary analyses demonstrated correlations between signal and severity of mood, anxiety, somatisation and global functioning symptoms. Conclusions These findings indicate the presence of aberrant connectivity in FS and extend the biopsychosocial network model by demonstrating that common aetiology is linked to both FS and comorbidities, but the overlap in affected networks varies by comorbid symptoms.
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