Abstract
BACKGROUND: Negative cognitive bias and aberrant neural processing of self-referent emotional words seem to be trait-marks of depression. However, it is unclear whether these neurocognitive changes are present in unaffected first-degree relatives and constitute an illness endophenotype.
METHODS: Fifty-three healthy, never-depressed monozygotic or dizygotic twins with a co-twin history of depression (high-risk group: n = 26) or no first-degree family history of depression (low-risk group: n = 27) underwent neurocognitive testing and functional magnetic imaging (fMRI) as part of a follow-up cohort study. Participants performed a self-referent emotional word categorisation task and free word recall task followed by a recognition task during fMRI. Participants also completed questionnaires assessing mood, personality traits and coping strategies.
RESULTS: High-risk and low-risk twins (age, mean ± SD: 40 ± 11) were well-balanced for demographic variables, mood, coping and neuroticism. High-risk twins showed lower accuracy during self-referent categorisation of emotional words independent of valence and more false recollections of negative words than low-risk twins during free recall. Functional MRI yielded no differences between high-risk and low-risk twins in retrieval-specific neural activity for positive or negative words or during the recognition of negative versus positive words within the hippocampus or prefrontal cortex.
CONCLUSIONS: The subtle display of negative recall bias is consistent with the hypothesis that self-referent negative memory bias is an endophenotype for depression. High-risk twins' lower categorisation accuracy adds to the evidence for valence-independent cognitive deficits in individuals at familial risk for depression.
Original language | English |
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Journal | Journal of Affective Disorders |
Volume | 226 |
Pages (from-to) | 267-273 |
Number of pages | 7 |
ISSN | 0165-0327 |
DOIs | |
Publication status | Published - 15 Jan 2018 |
Keywords
- Adult
- Brain Mapping
- Cognition Disorders
- Cohort Studies
- Depressive Disorder/physiopathology
- Emotions/physiology
- Endophenotypes
- Female
- Hippocampus/physiology
- Humans
- Magnetic Resonance Imaging
- Male
- Mental Recall
- Prefrontal Cortex/physiology
- Twins, Dizygotic
- Verbal Behavior/physiology
- Depression
- Cognition
- Familial risk
- Endophenotype
- FMRI