Common and exclusive spontaneous neural activity patterns underlying pure generalized anxiety disorder and comorbid generalized anxiety disorder and depression

• Published in: Journal of affective disorders Vol. 331; pp. 82 - 91
• Main Authors: Yan, Haohao, Han, Yiding, Shan, Xiaoxiao, Li, Huabing, Liu, Feng, Xie, Guojun, Li, Ping, Guo, Wenbin
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 15.06.2023
• Subjects: Anxiety Disorders - epidemiology; Brain - diagnostic imaging; Comorbidity; Depression; Fractional amplitude of low-frequency fluctuations; Generalized anxiety disorder; Humans; Longitudinal Studies; Magnetic Resonance Imaging; Psychiatric/Mental Health; Resting-state functional magnetic resonance imaging; Fractional amplitude of low-frequency fluctuations; Depression; Generalized anxiety disorder; Resting-state functional magnetic resonance imaging; Comorbidity
• ISSN: 0165-0327; 1573-2517; 1573-2517
• DOI: 10.1016/j.jad.2023.03.047

This study aimed to identify common and exclusive neural substrates underlying pure generalized anxiety disorder (GAD, G0) and comorbid GAD and depression (G1), assess whether they could assist in diagnosis and prediction of treatment response, and determine whether comorbid depression in GAD patients would change their neural plasticity. A longitudinal study was conducted, involving 98 patients (40 in the G0 group and 58 in the G1 group) and 54 healthy controls (HCs). The fractional amplitude of low-frequency fluctuations (fALFF), support vector machine, and support vector regression were employed. The shared neural underpinnings across the two subtypes of GAD were hyperactivity in the right cerebellar Crus II and inferior temporal gyrus and hypoactivity in the right postcentral gyrus. The G1 group showed hypoactivity in the frontal gyrus, compared with HCs, and hyperactivity in the middle temporal gyrus, compared with the G0 group or HCs. These alterations could aid in diagnosis and the prediction of treatment response with high accuracy. After treatment, both the G1 and G0 groups showed higher fALFF than those before treatment but were located in different brain regions. The study was performed in a single center and subjects showed a fairly homogeneous ethnicity. Common and exclusive neural substrates underlying the two subtypes of GAD were identified, which could assist in diagnosis and the prediction of treatment response. Pharmacotherapy for the two subtypes of GAD recruited different pathways, suggesting that comorbid depression in GAD patients would change their neural plasticity. •Common neural substrates of pure GAD and comorbid GAD and depression are identified.•Exclusive neural substrates of the two subtypes of GAD are identified.•Pharmacotherapy for the two subtypes of GAD recruits different pathways.•Comorbid depression in GAD patients changes their neural plasticity.