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Group cognitive behavioral therapy modulates the resting-state functional connectivity of amygdala-related network in patients with generalized social anxiety disorder
- Minlan Yuan†1,
- Hongru Zhu†1, 2,
- Changjian Qiu1,
- Yajing Meng1, 2,
- Yan Zhang1,
- Jing Shang1,
- Xiaojing Nie1,
- Zhengjia Ren1,
- Qiyong Gong3,
- Wei Zhang1, 2Email author and
- Su Lui3, 4Email author
© The Author(s). 2016
Received: 30 August 2015
Accepted: 6 June 2016
Published: 13 June 2016
Amygdala is considered as the core pathogenesis of generalized social anxiety disorder (GSAD). However, it is still unclear whether effective group cognitive behavioral therapy (CBT) could modulate the function of amygdala-related network. We aimed to examine the resting-state functional connectivity (rsFC) of the amygdala before and after group CBT.
Fifteen patients with GSAD were scanned on a 3T MR system before and after 8 weeks of group CBT. For comparison, nineteen healthy control participants also underwent baseline fMRI scanning. We used bilateral amygdala as seed regions and the rsFC maps of the right and left amygdala were created separately in a voxel-wise way. Clusters survived two-tailed Gaussian Random Field (GRF) correction at p <0.05 (voxel z value >2.3).
Compared with baseline, patients with CBT showed significantly decreased connectivity of the left amygdala with the right putamen, the left dorsal medial prefrontal cortex (dmPFC) and the right dorsal anterior cingulate cortex (dACC). Especially, the changes of the connectivity between the left amygdala and the dACC positively correlated with changes of the anxiety symptom in patients. Furthermore, in relative to controls, patients showed higher connectivity of left amygdala with dmPFC and dACC at baseline, while normal after CBT.
Short-term group CBT could down-regulate the abnormal higher connectivity of prefrontal-amygdala network, along with clinical improvement. This may provide a potential biomarker to monitor the treatment effect of CBT in GSAD patients.
Generalized social anxiety disorder (GSAD) is a common mental disorder that mainly involves a notable fear and avoidance of most social or performance situations,  and has a point prevalence of 4.4 % . The repeated experience of anxiety in relatively harmless situations interferes with substantial occupational performance and relationships of GSAD patients . Evidences from animal models [4, 5] and human beings [6, 7] have indicated the role of amygdala as the core in the pathogenesis of GSAD. Especially, neuroimaging studies have detected decreased volume of the amygdala  and increased functional activity of the amygdala in response to aversive and threatening social stimuli in GSAD patients [9–11]. Further studies began to study the interaction of amygdala with other brain regions since the GSAD are attributable to the mis-communication among different brain regions in a wide network rather than a single specific brain structure . Impaired connectivity between amygdala and anterior cingulate cortex (ACC) rather than the activity pattern of the amygdala has been found to be related to anxiety symptoms severity . Furthermore, anxiety was associated with a negative connectivity between amygdala and ventral medial prefrontal cortex (mPFC), suggesting disrupted emotion regulation. Besides, a positive connectivity between amygdala and dorsal mPFC was also related to anxiety, indicating hypervigilance to external stimuli . Abnormal amygdala connectivity with other brain regions such as precuneus  and insula  in GSAD have also been revealed.
However, another question raises that whether these aberrant amygdala-related networks can be modulated along with clinical improvement after treatment. Investigation of the brain changes before and after treatment not only improves our understanding of the pathogenesis and recovery of GSAD, but can also help to monitor treatment effects and guide the selection of the optimal therapy . The resting-state functional connectivity (rsFC) method has become a valuable tool for investigating network function, as it allows for a paradigm-free analysis of connectivity in fMRI without a priori assumptions about neural activation [18, 19]. Besides, the potentially powerful method enables us to increase our understanding and develop a more refined and comprehensive brain modulatory model of GSAD before and after treatment.
Using rsFC, some studies found the neuropeptide oxytocin could affect the rsFC of the amygdala with rostral ACC/ventral mPFC in GSAD patients . However, as another important treatment method , cognitive–behavioral therapy (CBT) appears to be equally effective but more enduring [22, 23] and safer, with fewer side effects. A recent study also showed that the resting-state amygdala-prefrontal connectivity at baseline could predict the prognosis of GSAD patients after CBT . It is still unclear that whether the standardized group CBT  could modulate amygdala-related functional connectivity along with clinical improvement. Based on the literature, we hypothesized that certain amygdala-related neural network was disrupted compared to healthy control subjects at baseline, which would be normalized by group CBT along with clinical improvement.
Demographic information and psychological variables in GSAD and HC groups before and after treatment
HC (n = 19)
Pretreatment GSAD (n = 15)
Posttreatment GSAD (n = 15)
T (pre-treatment vs HCs)
P (pre-treatment vs HCs)
T (pretreatment vs posttreatment)
P (pretreatment vs posttreatment)
26.26 ± 4.90
27.07 ± 8.11
15.95 ± 2.82
11.27 ± 3.35
Total LSAS (mean ± SD)
24.53 ± 17.23
78.87 ± 27.00
50.93 ± 19.13
LSAS fear (mean ± SD)
11.00 ± 9.68
38.13 ± 13.21
26.60 ± 8.80
LSAS avoid (mean ± SD)
13.53 ± 10.85
40.73 ± 15.22
24.33 ± 12.75
HAMA (mean ± SD)
2.21 ± 2.64
14.53 ± 8.51
9.33 ± 5.27
HAMD (mean ± SD)
2.11 ± 2.62
11.00 ± 6.75
7.00 ± 4.58
The psychiatric diagnostic classification of the participants was based on the Structured Clinical Interview for DSM-IV axis I disorders (SCID)  by psychiatrists. All participants were right-handed. The participants were interviewed to confirm that there was no history of psychiatric illness among their first-degree relatives, and that they themselves had no history of major medical or neurologic illness, and no history of substance abuse within a 6-month period prior to scanning. The patients had to fulfill the criteria for GSAD according to the SCID. The exclusion criteria for the patient group included current psychotherapy, past CBT, and other DSM-IV diagnoses, thus the patients included had no comorbidty.
Symptom severity was assessed using the Liebowitz Social Anxiety Scale Self-Report [27, 28] (LSAS-SR) at the time of inclusion in the study and after treatment. The Hamilton Anxiety Rating Scale (HAMA) and the Hamilton Depression Rating Scale (HAMD) were also used to measure anxiety and depression for all the participants.
Patients participated in 8 weekly CBT sessions in a group format according to the principles described by Hope, Heimberg  and Hofmann . The therapy consisted of one 150-min session per week, according to a standardized protocol-based group treatment . The sessions were conducted by a licensed clinical psychologist with several years of working experience in group CBT. A licensed clinical psychologist with expertise in both CBT and clinical trial studies involving CBT supervised the therapy to ensure adherence to treatment. The two psychologists were not involved in the subsequent analysis of treatment outcome and fMRI data. The group CBT comprised of psychoeducation, cognitive restructuring, relaxation training, in vivo exposures to public speaking, social skills training and homework assignment.
Functional MRI scan acquisition
A 3.0 T magnetic resonance scanner (Siemens 3.0 T Trio Tim, Germany) with a twelve-channel phased-array head coil at the Huaxi MR Research Center was used. Each participant was positioned supine in the MRI scanner with foam padding to reduce head movements. Functional images were acquired using a single-shot, gradient-recalled echo-planar imaging sequence (repetition time, 2,000 ms; echo time, 30 ms; flip angle, 90°; field of view, 240 mm × 240 mm; matrix, 64 × 64; thickness, 5 mm; without gap), which yielded a voxel size of 3.75 mm × 3.75 mm × 5 mm. Each brain volume comprised of 30 axial slices and each functional run contained 205 image volumes. Participants were instructed to rest with their eyes closed and let their minds wander but not fall asleep. The scan lasted 6.8 min.
Functional MRI data preprocessing
Imaging preprocessing was performed with Data Processing Assistant for Resting-State fMRI Basic Edition (DPARSF_3.0; http://rfmri.org/DPARSF). All software programs were run on a Statistical Parametric Mapping platform, (SPM8, http://www.fil.ion.ucl.ac.uk/spm), based on the MATLAB programming language (The Mathworks Inc, USA). The first 10 volumes from each run were discarded to ensure the stability of the imaging data. In the first step, the functional images were corrected for slice timing, and participants with head motion of more than 3.0 mm in the x, y, or z direction and more than 1.0° of rotation about each axis were excluded. Next, the realigned images were spatially normalized to the EPI template in SPM8, resampled to 3 mm cubic voxels, and smoothed by convolution with an isotropic Gaussian kernel (full width half maximum, 4 mm) to decrease spatial noise. Linear trend and quadratic trend entered in the regression analysis. Cerebrospinal fluid, white matter, 6 head motion parameters, 6 head motion parameters one time point before, and the 12 corresponding squared items were removed from the images . Considering the increasing evidence that global brain signal regression could alter inter-individual differences , the global signal regression was not performed. The resting data were bandpass-filtered between frequencies of 0.01 and 0.1 to limit the analysis to the resting-state frequencies of interest.
Functional MRI data analysis
By applying a seed-region approach , we used the right and left amygdala seeds, defined within the automated anatomical labeling (AAL)  atlas using MarsBar toolbox (http://marsbar.sourceforge.net) for FC analyses. The resulting r values were converted to z-values using Fisher's r-to-z transformation to improve the Gaussianity of their distribution. The FC maps of both the right and left amygdala were created using the resting-state fMRI data processing toolkit (REST V1.8, State Key Laboratory of Cognitive Neuroscience and Learning in Beijing Normal University; 〈http://www.restfmri.net/forum/REST_V1.8〉).
We then performed several statistical parametric tests in REST to test our priori hypotheses. To examine the changed amygdala-related network compared to the baseline status after group CBT, the FC maps in the pre-treatment and post-treatment groups were compared on a voxel-wise basis via a paired sample t-test. The Gaussian Random Field (GRF) theory correction was used for the statistical significance of group differences, with a voxel z threshold of a voxel p value <0.0214, a cluster p value <0.1 (two tailed), and a cluster connectivity of 5 mm, which is equivalent to voxel z value >2.3, cluster p value < 0.05 (two one tail corrections) in the SPM. Then, we defined regions of interest (ROI) based on functional clusters showing significant differences between pre-treatment and post-treatment groups. These seed regions were used as masks to test whether the pre- versus post-treatment findings in patients were different between patients and healthy controls (HC). Two sample t-test was used to characterize the difference between patients and controls (p < 0.05, voxel z value > 2.3, GRF corrected). Cluster size was set at least 5 voxels (135 mm3), with cluster connectivity of 5 mm. Gender, age, sex, education years and frame-wise displacement (FD) measurements of head motion  were modeled as covariates to remove their impacts.
After multiple comparison corrections, we further identified the surviving clusters by comparison with the neuroanatomical atlas by visual assessment and cross-referenced reports. Finally, the FC values of the seed regions and functional clusters within the seed regions that survived the voxel correction criteria between pre-treatment and HC groups were extracted by REST toolkit and used for further analysis. To assess for correlations with symptom severity, the extracted FC values from the GSAD pre-treatment scans were correlated with the LSAS (including total score, fear factor and avoidance factor) and HAMA using Pearson correlation analysis. Pearson correlation coefficient analysis was also conducted between the degree of change in the extracted FC values (ΔFC/PreFC) and the scale of improvement in LSAS (ΔLSAS/PreLSAS) and HAMA (ΔHAMA/PreHAMA) scores upon treatment in order to test the hypothesis that FC changes would parallel the clinical response to treatment. (SPSS version 19, IBM, USA).
After 8 weeks of group CBT, the total and the subscale scores of LSAS-SR significantly decreased (p < 0.05) in patients group, with the average total scores reduced from 78.87 ± 27.00 to 50.93 ± 19.13. Also, the HAMA scores reduced from an average of 14.53 ± 8.51 to 9.33 ± 5.27 (p < 0.05), while HAMA decreased from an average of 11.00 ± 6.75 to 7.00 ± 4.58 (p < 0.05). These findings indicate the CBT is effective in treatment of the symptoms of GSAD patients (Table 1).
Compared to the baseline, patients with GSAD showed decreased connectivity of the left amygdala with three brain regions: the right putamen, the left dorsal portions of the PFC (dmPFC), and the right dorsal ACC (dACC) (Figs. 1 and 2). No differences were found for the right amygdala connectivity between the pre-treatment and post-treatment groups. The changes of extracted FC values (ΔFC/PreFC) in left amygdala-right ACC were positively correlated with changes of the HAMA scores (ΔHAMA/PreHAMA) (r = 0.823, p <0.001). No significant correlation of extracted FC values from the GSAD pre-treatment scans and symptom severity was revealed.
Altered amygdala connectivity with other brain regions
Altered amygdala connectivity in GSAD patients before and after treatment
GSAD Pre > GSAD Post
Abnormal amygdala connectivity in pre-treatment group compared with HC
GSAD Pre > HC
Abnormal amygdala connectivity in post-treatment group compared with HC
In this longitudinal study, we used fMRI to investigate changes of rsFC in patients with GSAD before and after 8 weekly group CBT treatment. Based on a standard clinician measure, the majority of patients improved following treatment. As we hypothesized, GSAD patients showed aberrant amygdala-related network and the short-term group CBT could normalize the abnormal hyper-connectivity of amygdala-prefrontal network. Furthermore, the changes of the left amygdala-dACC connectivity were associated with the clinical improvement (changes of the HAMA scores) in GSAD patients after treatment.
The most important finding of the current study is the abnormally elevated amygdala-dACC connectivity in GSAD patients, which is normalized along with clinical symptom improvement after group CBT. The dACC is densely and reciprocally connected with amygdala  which mostly sends projections to amygdala . Moreover, joint activation pattern of amygdala and dACC have been identified in many neuroimaging studies on emotion [37, 38]. It has been previously reported that the dorsal–caudal regions of the ACC and mPFC are involved in the appraisal and expression of negative emotions, whereas the ventral–rostral portions of the ACC and mPFC play a regulatory role in negative emotion [39, 40]. The authors concluded that the amygdala-dmPFC/ACC connectivity is associated with “negative emotion generation” . Abnormal amygdala-dACC connectivity has been previously reported in association with anxiety [13, 40]. Considering the above mentioned findings, and in conjunction with our results, the abnormal hyper-connectivity of amygdala-dACC connectivity could attribute an exaggerated significance to possible threat stimuli from the internal and the external environment, leading to a high level of anxiety in patients with GSAD. Besides, present study provide further evidence to support the 8 weeks of group CBT exert an effect on normalizing the amygdala–dACC connectivity along with the improvement of anxiety symptom. Since CBT could alleviate the predisposition for excessive fear and anxiety in response to environmental stimuli  by effective strategies such as relaxation training, in vivo exposure and social skills training, such therapy could relief the abnormal elevated connectivity between amygdala and dACC. Therefore, our finding not only provided robust evidence for the key role of the amygdala-dACC connectivity in GSAD pathogenesis, but also provide a potential biomarker to monitor the treatment effect of CBT in GSAD patients.
Besides, we also found that the short-term group CBT reduced the abnormally elevated connectivity of the left amygdala with the left dmPFC at baseline. In fact, the abnormal elevated amygdala-dmPFC connectivity has been reported during self-directed criticism in patients with generalized social phobia . Both the dmPFC and the amygdala are regions associated with fear expression in response to stimuli from the external world and a positive amygdala-dmPFC connectivity was associated with hypervigilance . Thus the observed impaired amygdala–dmPFC connectivity in our study may reflect the tendency to attribute an exaggerated significance to possible self-relevant stimuli from the processed threat cues in patients with GSAD [42, 43]. And the decreased coupling of these two regions after cognitive restructuring in group CBT could underlie this modulated knowledge of the self.
Beyond the above findings, we found decreased connectivity between the left amygdala and the right putamen in GSAD after treatment. The putamen is the one of the sectors of the striatum. The striatum has been proved to be the “emotion guarder”, which was an important terminal to receive the sensory and emotional information from the prefrontal areas . Thus the decreased connectivity between the left amygdala and the right putamen in SAD may represent the short-term recovery process of the negtive emotions in social situations.
Another thing should be noted is that the altered connectivity only involved the left amygdala. This phenomenon could be explained by the abundantly reported lateralization of the human amygdala. The left amygdala was more often activated than the right amygdala, irrelevant to stimulus type . Our finding of left amygdala-dominant brain networks at resting-state further suggested the asymmetric interhemispheric information transfer, in line with the left hemifield of amygdala advantage for fear processing in task-related studies .
The findings of the present study should be considered in the context of several limitations. First, the study design lacked re-test data of the healthy control group and a placebo or wait-list control. Thus, the neural and clinical findings cannot be causally attributed to group CBT and could be related to a number of plausible factors not related to the treatment, such as the natural course of the illness over the 8-week period and placebo/expectancy effects. Second, four of the GSAD patients were on SSRI medication at the time of study participation and the medications were reported to be ineffective in the treatment of this illness. However, the effects of medication should not be ignored in explaining the results. A recent study showed mediating effects of acute SSRI intake on prefrontal-amygdala effectivity connectivity , although the patients withdrawed medication at least two weeks before the baseline MRI scan in present study, our findings might be related to the medications. Third, although from previous studies we know that a group of 14 participants were sufficient to detect significant treatment effects measured with fMRI , the limited sample size (n = 15 GSAD subjects) increased the risk for false negatives and constrains the test for relationships between rsFC and treatment effects. These findings, however, may guide subsequent fMRI studies of treatment. Finally, there are a number of studies suggesting distinct functional connectivity patterns for the amygdala subregions such as the superficial and centromedial amygdala when choosing these subnuclei as seed [49, 50]. However, accurate delineation in the human brain is still under debate  and such approach has a major limitation as the amygdala is peculiarly susceptible to image distortion, normalization failure and draining vein effects . Thus we chose a more conservative approach based on functional results of the whole amygdala region using the AAL template according to most human literature for investigation of the amygdala-related network.
Our findings provide evidence that the short-term group CBT could attenuate the hyper-connectivity of amygdala with dACC and dmPFC along with the improvement of symptom severity during resting-state in patients with generalized social anxiety disorder. These findings not only provided robust evidence for the key role of the abnormal higher connectivity of prefrontal-amygdala in GSAD pathogenesis, but also provide a potential biomarker to monitor the treatment effect of CBT in GSAD patients.
This work was supported by the National Natural Science Foundation of China (grant nos. 81371484, 81222018, 81030027, 81227002 and 81220108013); National Key Technologies R&D Program (program no. 2012BAI01B03); the 863 Program (grant no. 2008AA02Z408); the 973 Project (grant no. 2008CB517407); the Support Plan of Sichuan (grant nos. 2011SZ0292, 2014GZ0143). This research received no specific grant from any funding agency, commercial or not-for-profit sectors.
The authors gratefully acknowledge the contributions of Hehan Tang, Yuchen Li, and Ye Zhang.
Availability of data and materials
The data will not be made available in order to protect the participants identity.
Authors MY and HZ participanted in the projects design, fMRI scan acquisition, and carried out the fMRI data preprocessing, fMRI data analysis and the manuscript drafting. Authors WZ, SL and QG designed and conceived of the study, and participated in its coordination and helped to draft the manuscript. Authors CQ, YM, YZ and JS participanted in the projects design, recruited the participants and finished the clinical assessment. Authos XN and ZR also recruited the sample and were responsible for the integrity and accuracy of the data. All authors have read and approved the final version of the manuscript.
The authors declare that they have no competing interests.
Consent for publication
Publication of clinical data and information was obtained.
Ethics approval and consent to participate
All participants were informed about the study and provided written informed consent before the study, which was approved by the Medical Research Ethics Committee of West China Hospital, Sichuan University.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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