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Neural response to emotional faces in monozygotic twins: association with familial risk of affective disorders
- Source :
-
Journal of psychiatry & neuroscience : JPN [J Psychiatry Neurosci] 2019 Jul 01; Vol. 44 (4), pp. 277-286. - Publication Year :
- 2019
-
Abstract
- Background: Aberrant neural and cognitive response to emotional faces has been observed in people at familial risk of an affective disorder. In this functional MRI study of monozygotic twins, we explored neural correlates of the attentional avoidance of emotional faces that we had previously observed in high-risk versus affected twins, and whether an abnormal neural response to emotional faces represents a risk endophenotype.<br />Methods: We recruited unaffected monozygotic twins with a co-twin history of mood episodes (high-risk), monozygotic twins with previous mood episodes (affected) and monozygotic twins with no personal or first-degree history of mood episodes (low-risk) between December 2014 and January 2017 based on a nationwide register linkage. Participants viewed fearful and happy faces while performing a gender discrimination task during functional MRI (fMRI) and performed emotional faces dot-probe and facial expression recognition tasks outside the scanner.<br />Results: A total of 129 monozygotic twins underwent whole-brain fMRI. Highrisk twins (n = 38) displayed greater medial and superior prefrontal response to emotional faces than affected twins (n = 62). This greater activity correlated with stronger attentional avoidance of emotional faces in high-risk twins. In contrast, high-risk and affected twins showed no aberrant neural activity to emotional faces compared with low-risk twins (n = 29).<br />Limitations: A limitation of this study was its cross-sectional design.<br />Conclusion: Greater recruitment of the medial and superior prefrontal cortex during implicit emotion processing in high-risk versus affected twins may represent a compensatory or resilience mechanism. In contrast, aberrant neural response to emotional faces does not seem to be a risk endophenotype for affective disorders.<br />Competing Interests: C. Harmer has received consultancy fees from P1vital Ltd, Lundbeck, Servier and Eli-Lilly, and is a company director of Oxford Psychologists Ltd. She has also received grant income from GSK, UCB, Janssen Inc, Lundbeck, Servier and AstraZeneca. H. Siebner discloses honoraria as journal editor from Elsevier Publishers and book editor from Springer Publishing, as well as honoraria as speaker from Genzyme and MerckSerono, and grant support from Biogen-idec within the last 3 years. M. Vinberg discloses consultancy fees from Lundbeck within the last 3 years. L. Kessing has been a consultant for Sunovion within the last 3 years. K. Miskowiak reports having received consultancy fees from Lundbeck and Allergan in the past 3 years. No other competing interests declared.<br /> (© 2019 Joule Inc. or its licensors)
- Subjects :
- Adult
Cross-Sectional Studies
Endophenotypes
Female
Humans
Magnetic Resonance Imaging
Male
Prefrontal Cortex diagnostic imaging
Risk
Twins, Monozygotic
Young Adult
Emotions physiology
Facial Expression
Facial Recognition physiology
Genetic Predisposition to Disease
Mood Disorders physiopathology
Prefrontal Cortex physiopathology
Subjects
Details
- Language :
- English
- ISSN :
- 1488-2434
- Volume :
- 44
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of psychiatry & neuroscience : JPN
- Publication Type :
- Academic Journal
- Accession number :
- 30942564
- Full Text :
- https://doi.org/10.1503/jpn.170246