Journal
PSYCHOLOGICAL MEDICINE
Volume 53, Issue 6, Pages 2328-2338Publisher
CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291721004165
Keywords
Cluster-analysis; emotional cognition; emotional processing; emotional regulation; endophenotype; mood disorders; relatives; resilience; risk
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The study found distinct emotional cognition profiles in healthy first-degree relatives of patients with MDD and BD, including an "emotionally preserved" cluster and an "emotionally blunted" cluster. The "emotionally blunted" relatives showed poorer neurocognitive performance, heightened subsyndromal mania symptoms, lower education levels, and difficulties with interpersonal functioning compared to controls, while the "emotionally preserved" relatives were comparable to controls in these aspects.
Background Patients with major depressive disorder (MDD) or bipolar disorder (BD) exhibit difficulties with emotional cognition even during remission. There is evidence for aberrant emotional cognition in unaffected relatives of patients with these mood disorders, but studies are conflicting. We aimed to investigate whether emotional cognition in unaffected first-degree relatives of patients with mood disorders is characterised by heterogeneity using a data-driven approach. Methods Data from 94 unaffected relatives (33 of MDD patients; 61 of BD patients) and 203 healthy controls were pooled from two cohort studies. Emotional cognition was assessed with the Social Scenarios Test, Facial Expression Recognition Test and Faces Dot-Probe Test. Hierarchical cluster analysis was conducted using emotional cognition data from the 94 unaffected relatives. The resulting emotional cognition clusters and controls were compared for emotional and non-emotional cognition, demographic characteristics and functioning. Results Two distinct clusters of unaffected relatives were identified: a relatively 'emotionally preserved' cluster (55%; 40% relatives of MDD probands) and an 'emotionally blunted' cluster (45%; 29% relatives of MDD probands). 'Emotionally blunted' relatives presented with poorer neurocognitive performance (global cognition p = 0.010), heightened subsyndromal mania symptoms (p = 0.004), lower years of education (p = 0.004) and difficulties with interpersonal functioning (p = 0.005) than controls, whereas 'emotionally preserved' relatives were comparable to controls on these measures. Conclusions Our findings show discrete emotional cognition profiles that occur across healthy first-degree relatives of patients with MDD and BD. These emotional cognition clusters may provide insight into emotional cognitive markers of genetically distinct subgroups of individuals at familial risk of mood disorders.
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