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Dissociations in cortical thickness and surface area in non-comorbid never-treated patients with social anxiety disorder

Authors :
Su Lui
Xiaoqi Huang
Graham J. Kemp
Qiyong Gong
Song Wang
Lihua Qiu
Xun Zhang
Qiang Luo
Nanfang Pan
Weihong Kuang
Xun Yang
Source :
EBioMedicine, Vol 58, Iss, Pp 102910-(2020), EBIOMEDICINE
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Background Abnormalities of functional activation and cortical volume in brain regions involved in the neurobiology of fear and anxiety have been implicated in the pathophysiology of social anxiety disorder (SAD). However, few studies have performed separate measurements of cortical thickness (CT) and cortical surface area (CSA) which reflect different neurobiological processes. Thus, we aimed to explore the cortical morphological anomaly separately in SAD using FreeSurfer. Methods High-resolution structural magnetic resonance images were obtained from 32 non-comorbid never-treated adult SAD patients and 32 demography-matched healthy controls. Cortical morphometry indices including CT and CSA were separately determined by FreeSurfer and compared between the two groups via whole-brain vertex-wise analysis, while partial correlation analysis using age and gender as covariates were conducted. Findings The patients with SAD showed decreased CT but increased CSA near-symmetrically in the bilateral prefrontal cortex (PFC) of the dorsolateral, dorsomedial, and ventromedial subdivisions, as well as the right lateral orbitofrontal cortex; increased CSA in the left superior temporal gyrus (STG) was also observed in SAD. The CSA in the left PFC was negatively correlated with the disease duration. Interpretation As the balloon model hypothesis suggests that the tangentially stretched cortex may cause dissociations in cortical morphometry and affect the cortical capacity for information processing, our findings of dissociated morphological alterations in the PFC and cortical expansion in the STG may reflect the morphological alterations of the functional reorganization in those regions, and highlight the important role of those structures in the pathophysiology and neurobiology of SAD. Funding This study was funded by the National Natural Science Foundation of China (Grant Nos. 31700964 , 31800963 , 81621003 , and 81820108018 ).

Details

ISSN :
23523964
Volume :
58
Database :
OpenAIRE
Journal :
EBioMedicine
Accession number :
edsair.doi.dedup.....5f9d957dc0bd1d1e345f3316d25c6e17
Full Text :
https://doi.org/10.1016/j.ebiom.2020.102910