Literature DB >> 33150947

Patients with anxiety disorders rely on bilateral dlPFC activation during verbal working memory.

Nicholas L Balderston1,2, Elizabeth Flook1, Abigail Hsiung1, Jeffrey Liu1, Amanda Thongarong1, Sara Stahl1, Walid Makhoul2, Yvette Sheline2, Monique Ernst1, Christian Grillon1.   

Abstract

One of the hallmarks of anxiety disorders is impaired cognitive control, affecting working memory (WM). The dorsolateral prefrontal cortex (dlPFC) is critical for WM; however, it is still unclear how dlPFC activity relates to WM impairments in patients. Forty-one healthy volunteers and 32 anxiety (general and/or social anxiety disorder) patients completed the Sternberg WM paradigm during safety and unpredictable shock threat. On each trial, a series of letters was presented, followed by brief retention and response intervals. On low- and high-load trials, subjects retained the series (five and eight letters, respectively) in the original order, while on sort trials, subjects rearranged the series (five letters) in alphabetical order. We sampled the blood oxygenation level-dependent activity during retention using a bilateral anatomical dlPFC mask. Compared to controls, patients showed increased reaction time during high-load trials, greater right dlPFC activity and reduced dlPFC activity during threat. These results suggest that WM performance for patients and controls may rely on distinct patterns of dlPFC activity with patients requiring bilateral dlPFC activity. These results are consistent with reduced efficiency of WM in anxiety patients. This reduced efficiency may be due to an inefficient allocation of dlPFC resources across hemispheres or a decreased overall dlPFC capacity. Published by Oxford University Press 2020. This work is written by (a) US Government employee(s) and is in the public domain in the US.

Entities:  

Keywords:  dorsolateral prefrontal cortex; functional magnetic resonance imaging; generalized anxiety disorder; social anxiety disorder; threat; working memory

Mesh:

Year:  2020        PMID: 33150947      PMCID: PMC7759210          DOI: 10.1093/scan/nsaa146

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


  67 in total

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