Psychopathic traits influence amygdala-anterior cingulate cortex connectivity during facial emotion processing
Abstract
There is accumulating evidence that youths with antisocial behavior or psychopathic traits show deficits in facial emotion recognition, but little is known about the neural mechanisms underlying these impairments. A number of neuroimaging studies have investigated brain activity during facial emotion processing in youths with Conduct Disorder (CD) and adults with psychopathy, but few of these studies tested for group differences in effective connectivity—i.e. changes in connectivity during emotion processing. Using functional magnetic resonance imaging and psycho-physiological interaction methods, we investigated the impact of CD and psychopathic traits on amygdala activity and effective connectivity in 46 male youths with CD and 25 typically-developing controls when processing emotional faces. All participants were aged 16–21 years. Relative to controls, youths with CD showed reduced amygdala activity when processing angry or sad faces relative to neutral faces, but the groups did not significantly differ in amygdala-related effective connectivity. In contrast, psychopathic traits were negatively correlated with amygdala–ventral anterior cingulate cortex connectivity for angry vs neutral faces, but were unrelated to amygdala responses to angry or sad faces. These findings suggest that CD and psychopathic traits have differential effects on amygdala activation and functional interactions between limbic regions during facial emotion processing.
Additional Information
© The Author(s) (2018). Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. Received: 26 July 2017; Revision Received: 12 February 2018; Accepted: 25 March 2018; Published: 12 April 2018. This study was supported by the Medical Research Council (MRC) through project code MC-A060-5PQ50 (to A.J.C.), a project grant from the Wellcome Trust (083140 to G.F. and I.M.G.), the Betty Behrens Research Fellowship at Clare Hall, University of Cambridge (to L.P.) and MRC research grant MR/P01271X/1 (to L.P.). Conflict of interest: None declared.Attached Files
Published - nsy019.pdf
Supplemental Material - nsy019_scan-17-334.pdf
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Additional details
- PMCID
- PMC6007413
- Eprint ID
- 86004
- Resolver ID
- CaltechAUTHORS:20180423-100305988
- Medical Research Council (UK)
- MC-A060-5PQ50
- Wellcome Trust
- 083140
- University of Cambridge
- Medical Research Council (UK)
- MR/P01271X/1
- Created
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2018-04-25Created from EPrint's datestamp field
- Updated
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2021-11-15Created from EPrint's last_modified field