Predicting treatment outcomes in patients with panic disorder: Cross-sectional and two-year longitudinal structural connectome analysis using machine learning methods

被引:0
|
作者
Pae, Chongwon [1 ]
Kim, Hyun-Ju [1 ]
Bang, Minji [1 ]
Park, Chun Il [1 ]
Lee, Sang-Hyuk [1 ]
机构
[1] CHA Univ, Sch Med, CHA Bundang Med Ctr, Dept Psychiat, Seongnam, South Korea
基金
新加坡国家研究基金会;
关键词
Panic disorder; Machine learning; Connectome; Treatment outcome; Longitudinal studies; MULTIVARIATE PATTERN-ANALYSIS; NEUROANATOMICAL HYPOTHESIS; REMITTED; 1ST-EPISODE; PREFRONTAL CORTEX; ANXIETY DISORDER; WHITE-MATTER; EARLY TRAUMA; GRAY-MATTER; NETWORK; INDIVIDUALS;
D O I
10.1016/j.janxdis.2024.102895
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Purpose: This study examined the relationship between structural brain networks and long-term treatment outcomes in patients with panic disorder (PD) using machine learning methods. Method: The study involved 80 participants (53 PD patients and 27 healthy controls) and included clinical assessments and MRI scans at baseline and after two years (160 MRIs). Patients were categorized based on their response to two-year pharmacotherapy. Brain networks were analyzed using white matter tractography and network-based statistics. Results: Results showed structural network changes in PD patients, particularly in the extended fear network, including frontal regions, thalamus, and cingulate gyrus. Longitudinal analysis revealed that increased connections to the amygdala, hippocampus, and insula were associated with better treatment response. Conversely, overconnectivity in the amygdala and insula at baseline was associated with poor response, and similar patterns were found in the insula and parieto-occipital cortex related to non-remission. This study found that SVM and CPM could effectively predict treatment outcomes based on network pattern changes in PD. Conclusions: These findings suggest that monitoring structural connectome changes in limbic and paralimbic regions is critical for understanding PD and tailoring treatment. The study highlights the potential of using personalized biomarkers to develop individualized treatment strategies for PD.
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页数:12
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