Literature DB >> 25344944

Neural changes with attention bias modification for anxiety: a randomized trial.

Jennifer C Britton1, Jenna G Suway2, Michelle A Clementi2, Nathan A Fox3, Daniel S Pine3, Yair Bar-Haim3.   

Abstract

Attention bias modification (ABM) procedures typically reduce anxiety symptoms, yet little is known about the neural changes associated with this behavioral treatment. Healthy adults with high social anxiety symptoms (n = 53) were randomized to receive either active or placebo ABM. Unlike placebo ABM, active ABM aimed to train individuals' attention away from threat. Using the dot-probe task, threat-related attention bias was measured during magnetic resonance imaging before and after acute and extended training over 4 weeks. A subset of participants completed all procedures (n = 30, 15 per group). Group differences in neural activation were identified using standard analyses. Linear regression tested predictive factors of symptom reduction (i.e., training group, baseline indices of threat bias). The active and placebo groups exhibited different patterns of right and left amygdala activation with training. Across all participants irrespective of group, individuals with greater left amygdala activation in the threat-bias contrast prior to training exhibited greater symptom reduction. After accounting for baseline amygdala activation, greater symptom reduction was associated with assignment to the active training group. Greater left amygdala activation at baseline predicted reductions in social anxiety symptoms following ABM. Further research is needed to clarify brain-behavior mechanisms associated with ABM training. Published by Oxford University Press 2014. This work is written by US Government employees and is in the public domain in the US.

Entities:  

Keywords:  amygdala; anxiety; attention training; dot-probe; fMRI; treatment

Mesh:

Year:  2014        PMID: 25344944      PMCID: PMC4483563          DOI: 10.1093/scan/nsu141

Source DB:  PubMed          Journal:  Soc Cogn Affect Neurosci        ISSN: 1749-5016            Impact factor:   3.436


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