Attentional processes during emotional face perception in social anxiety disorder: A systematic review and meta-analysis of eye-tracking findings

Author(s):  
Vivien Günther ◽  
Adam Kropidlowski ◽  
Frank Martin Schmidt ◽  
Katja Koelkebeck ◽  
Anette Kersting ◽  
...  
2014 ◽  
Vol 1 (5) ◽  
pp. 368-376 ◽  
Author(s):  
Evan Mayo-Wilson ◽  
Sofia Dias ◽  
Ifigeneia Mavranezouli ◽  
Kayleigh Kew ◽  
David M Clark ◽  
...  

2019 ◽  
Vol 32 (1) ◽  
Author(s):  
Rianne Gomes e Claudino ◽  
Laysa Karen Soares de Lima ◽  
Erickson Duarte Bonifácio de Assis ◽  
Nelson Torro

2021 ◽  
Vol 12 ◽  
Author(s):  
Johan Lundin Kleberg ◽  
Emilie Bäcklin Löwenberg ◽  
Jennifer Y. F. Lau ◽  
Eva Serlachius ◽  
Jens Högström

Background: Social anxiety disorder (SAD) has its typical onset in childhood and adolescence. Maladaptive processing of social information may contribute to the etiology and maintenance of SAD. During face perception, individuals execute a succession of visual fixations known as a scanpath which facilitates information processing. Atypically long scanpaths have been reported in adults with SAD, but no data exists from pediatric samples. SAD has also been linked to atypical arousal during face perception. Both metrics were examined in one of the largest eye-tracking studies of pediatric SAD to date.Methods: Participants were children and adolescents with SAD (n = 61) and healthy controls (n = 39) with a mean age of 14 years (range 10–17) who completed an emotion recognition task. The visual scanpath and pupil dilation (an indirect index of arousal) were examined using eye tracking.Results: Scanpaths of youth with SAD were shorter, less distributed, and consisted of a smaller number of fixations than those of healthy controls. These findings were supported by both frequentist and Bayesian statistics. Higher pupil dilation was also observed in the SAD group, but despite a statistically significant group difference, this result was not supported by the Bayesian analysis.Conclusions: The results were contrary to findings from adult studies, but similar to what has been reported in neurodevelopmental conditions associated with social interaction impairments. Restricted scanpaths may disrupt holistic representation of faces known to favor adaptive social understanding.


2020 ◽  
Vol 32 (4) ◽  
pp. 169-176
Author(s):  
Taryn Williams ◽  
Michael McCaul ◽  
Guido Schwarzer ◽  
Andrea Cipriani ◽  
Dan J Stein ◽  
...  

AbstractObjective:The aim of this paper was to provide a systematic review and update on the pharmacotherapy of social anxiety disorder (SAD), including the efficacy and tolerability of these agents, the ranking of interventions, and the grading of results by quality of evidence.Methods:The Common Mental Disorder Controlled Trial Register and two trial registries were searched for randomised controlled trials (RCTs) comparing any pharmacological intervention or placebo in the treatment of SAD. We performed a standard pairwise meta-analysis using a random effects model and carried out a network meta-analysis (NMA) using the statistical package, R. Quality of evidence was also assessed.Results:We included 67 RCTs in the review and 21 to 45 interventions in the NMA. Paroxetine was most effective in the reduction of symptom severity as compared to placebo. Superior response to treatment was also observed for paroxetine, brofaromine, bromazepam, clonazepam, escitalopram, fluvoxamine, phenelzine, and sertraline. Higher dropout rates were found for fluvoxamine. Brofaromine, escitalopram, fluvoxamine, paroxetine, pregabalin, sertraline, and venlafaxine performed worse in comparison to placebo for the outcome of dropouts due to adverse events. Olanzapine yielded a relatively high rank for treatment efficacy and buspirone the worse rank for dropouts due to any cause.Conclusion:The differences between drugs and placebo were small, apart from a significant reduction in symptom severity and response for paroxetine. We suggest paroxetine as a first-line treatment of SAD, with the consideration of future research on the drug olanzapine as well as brofaromine, bromazepam, clonazepam, escitalopram, fluvoxamine, phenelzine, and sertraline because we observed a response to treatment.


2019 ◽  
Vol 208 ◽  
pp. 25-33 ◽  
Author(s):  
Carla McEnery ◽  
Michelle H. Lim ◽  
Hailey Tremain ◽  
Ann Knowles ◽  
Mario Alvarez-Jimenez

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