%A Yao,Zhijun %A Liao,Mei %A Hu,Tao %A Zhang,Zhe %A Zhao,Yu %A Zheng,Fang %A Gutknecht,Jürg %A Majoe,Dennis %A Hu,Bin %A Li,Lingjiang %D 2017 %J Frontiers in Human Neuroscience %C %F %G English %K adolescent generalized anxiety disorder,Temporal properties,Dynamic Functional Connectivity,resting fMRI,biomarker. %Q %R 10.3389/fnhum.2017.00492 %W %L %M %P %7 %8 2017-October-13 %9 Original Research %+ Bin Hu,Key Laboratory of Wearable Computing of Gansu Province, Lanzhou University,China,bh@lzu.edu.cn %+ Lingjiang Li,Mental Health Institute, The Second Xiangya Hospital of Central South University,China,bh@lzu.edu.cn %# %! Identification of adolescent generalized anxiety disorder %* %< %T An Effective Method to Identify Adolescent Generalized Anxiety Disorder by Temporal Features of Dynamic Functional Connectivity %U https://www.frontiersin.org/articles/10.3389/fnhum.2017.00492 %V 11 %0 JOURNAL ARTICLE %@ 1662-5161 %X Generalized anxiety disorder (GAD) is one of common anxiety disorders in adolescents. Although adolescents with GAD are thought to be at high risk for other mental diseases, the disease-specific alterations have not been adequately explored. Recent studies have revealed the abnormal functional connectivity (FC) in adolescents with GAD. Most previous researches have investigated the static FC which ignores the fluctuations of FC over time and focused on the structures of “fear circuit”. To figure out the alterations of dynamic FC caused by GAD and the possibilities of dynamic FC as biomarkers, we propose an effective approach to identify adolescent GAD using temporal features derived from dynamic FC. In our study, the instantaneous synchronization of pairwise signals was estimated as dynamic FC. The Hurst exponent (H) and variance, indicating regularity and variable degree of a time series respectively, were calculated as temporal features of dynamic FC. By leave-one-out cross-validation (LOOCV), a relatively high accuracy of 88.46% could be achieved when H and variance of dynamic FC were combined as features. In addition, we identified the disease-related regions, including regions belonging to default mode (DM) and cerebellar networks. The results suggest that temporal features of dynamic FC could achieve a clinically acceptable diagnostic power and serve as biomarkers of adolescent GAD. Furthermore, our work could be helpful in understanding the pathophysiological mechanism of adolescent GAD.