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Empirical evidence for cognitive subgroups in body dysmorphic disorder.
Amy Malcolm1, Sarah N Brennan1,2, Sally A Grace1
1Centre for Mental Health, Faculty of Health, Arts & Design, Swinburne University of Technology, Hawthorn, VIC, Australia.
Cognitive functioning in body dysmorphic disorder (BDD) is not uniform; this study identified two subgroups: one with mild impairments and another with broadly impaired cognition. These findings highlight BDD
Area of Science:
- Psychiatry
- Neuroscience
- Cognitive Psychology
Background:
- Understanding cognitive functioning in body dysmorphic disorder (BDD) is limited due to small sample sizes and restricted cognitive domain assessments.
- Previous research presents inconsistent findings regarding cognition in BDD, suggesting potential cognitive heterogeneity.
Purpose of the Study:
- To comprehensively examine the cognitive profile of individuals with BDD across eight distinct cognitive domains.
- To investigate the existence of distinct cognitive subgroups within the BDD population.
Main Methods:
- Compared cognitive performance in 65 BDD patients and 70 healthy controls across inhibition/flexibility, working memory, processing speed, reasoning, learning, attention, and social cognition.
- Employed hierarchical clustering analysis on the cognitive data of the BDD group to identify potential subgroups.
Main Results:
- BDD patients exhibited significantly poorer cognitive functioning than controls in most domains, excluding attention/vigilance and social cognition.
- Cluster analysis revealed two subgroups: one with broadly intact cognition (72.3%) and another with broadly impaired cognition (27.7%).
- These cognitive subgroups did not significantly differ in clinical or sociodemographic characteristics.
Conclusions:
- Cognitive functioning in BDD is characterized by heterogeneity rather than uniform deficits.
- The identified subgroups suggest that broadly impaired cognition in a subset of individuals may account for group-level differences.
- The dissociation between cognitive profiles and clinical features has implications for understanding BDD etiology.
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