Emotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Emotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders. / Kjærstad, Hanne Lie; Varo, Cristina; Meluken, Iselin; Vieta, Eduard; Vinberg, Maj; Kessing, Lars Vedel; Miskowiak, Kamilla Woznica.

I: Psychological Medicine, Bind 53, Nr. 6, 2023, s. 2328-2338.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Kjærstad, HL, Varo, C, Meluken, I, Vieta, E, Vinberg, M, Kessing, LV & Miskowiak, KW 2023, 'Emotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders', Psychological Medicine, bind 53, nr. 6, s. 2328-2338. https://doi.org/10.1017/S0033291721004165

APA

Kjærstad, H. L., Varo, C., Meluken, I., Vieta, E., Vinberg, M., Kessing, L. V., & Miskowiak, K. W. (2023). Emotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders. Psychological Medicine, 53(6), 2328-2338. https://doi.org/10.1017/S0033291721004165

Vancouver

Kjærstad HL, Varo C, Meluken I, Vieta E, Vinberg M, Kessing LV o.a. Emotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders. Psychological Medicine. 2023;53(6):2328-2338. https://doi.org/10.1017/S0033291721004165

Author

Kjærstad, Hanne Lie ; Varo, Cristina ; Meluken, Iselin ; Vieta, Eduard ; Vinberg, Maj ; Kessing, Lars Vedel ; Miskowiak, Kamilla Woznica. / Emotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders. I: Psychological Medicine. 2023 ; Bind 53, Nr. 6. s. 2328-2338.

Bibtex

@article{f7efbb690cf446a3abf2286aaceac330,
title = "Emotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders",
abstract = "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. ",
keywords = "Cluster-analysis, emotional cognition, emotional processing, emotional regulation, endophenotype, mood disorders, relatives, resilience, risk",
author = "Kj{\ae}rstad, {Hanne Lie} and Cristina Varo and Iselin Meluken and Eduard Vieta and Maj Vinberg and Kessing, {Lars Vedel} and Miskowiak, {Kamilla Woznica}",
note = "Publisher Copyright: Copyright {\textcopyright} The Author(s), 2021. Published by Cambridge University Press.",
year = "2023",
doi = "10.1017/S0033291721004165",
language = "English",
volume = "53",
pages = "2328--2338",
journal = "Psychological Medicine",
issn = "0033-2917",
publisher = "Cambridge University Press",
number = "6",

}

RIS

TY - JOUR

T1 - Emotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders

AU - Kjærstad, Hanne Lie

AU - Varo, Cristina

AU - Meluken, Iselin

AU - Vieta, Eduard

AU - Vinberg, Maj

AU - Kessing, Lars Vedel

AU - Miskowiak, Kamilla Woznica

N1 - Publisher Copyright: Copyright © The Author(s), 2021. Published by Cambridge University Press.

PY - 2023

Y1 - 2023

N2 - 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.

AB - 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.

KW - Cluster-analysis

KW - emotional cognition

KW - emotional processing

KW - emotional regulation

KW - endophenotype

KW - mood disorders

KW - relatives

KW - resilience

KW - risk

U2 - 10.1017/S0033291721004165

DO - 10.1017/S0033291721004165

M3 - Journal article

C2 - 37310310

AN - SCOPUS:85118312669

VL - 53

SP - 2328

EP - 2338

JO - Psychological Medicine

JF - Psychological Medicine

SN - 0033-2917

IS - 6

ER -

ID: 363361143