Aberrant cognition in newly diagnosed patients with bipolar disorder and their unaffected relatives

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Aberrant cognition in newly diagnosed patients with bipolar disorder and their unaffected relatives. / Kjærstad, Hanne Lie; Mistarz, Nicolaj; Coello, Klara; Stanislaus, Sharleny; Melbye, Sigurd Arne; Harmer, Catherine J.; Vinberg, Maj; Miskowiak, Kamilla; Kessing, Lars Vedel.

I: Psychological Medicine, Bind 50, Nr. 11, 2020, s. 1808-1819.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Kjærstad, HL, Mistarz, N, Coello, K, Stanislaus, S, Melbye, SA, Harmer, CJ, Vinberg, M, Miskowiak, K & Kessing, LV 2020, 'Aberrant cognition in newly diagnosed patients with bipolar disorder and their unaffected relatives', Psychological Medicine, bind 50, nr. 11, s. 1808-1819. https://doi.org/10.1017/S0033291719001867

APA

Kjærstad, H. L., Mistarz, N., Coello, K., Stanislaus, S., Melbye, S. A., Harmer, C. J., Vinberg, M., Miskowiak, K., & Kessing, L. V. (2020). Aberrant cognition in newly diagnosed patients with bipolar disorder and their unaffected relatives. Psychological Medicine, 50(11), 1808-1819. https://doi.org/10.1017/S0033291719001867

Vancouver

Kjærstad HL, Mistarz N, Coello K, Stanislaus S, Melbye SA, Harmer CJ o.a. Aberrant cognition in newly diagnosed patients with bipolar disorder and their unaffected relatives. Psychological Medicine. 2020;50(11):1808-1819. https://doi.org/10.1017/S0033291719001867

Author

Kjærstad, Hanne Lie ; Mistarz, Nicolaj ; Coello, Klara ; Stanislaus, Sharleny ; Melbye, Sigurd Arne ; Harmer, Catherine J. ; Vinberg, Maj ; Miskowiak, Kamilla ; Kessing, Lars Vedel. / Aberrant cognition in newly diagnosed patients with bipolar disorder and their unaffected relatives. I: Psychological Medicine. 2020 ; Bind 50, Nr. 11. s. 1808-1819.

Bibtex

@article{2e30606f54b940dcaa1537799c8ffe97,
title = "Aberrant cognition in newly diagnosed patients with bipolar disorder and their unaffected relatives",
abstract = " Background:Patients with bipolar disorder (BD) experience persistent impairments in both affective and non-affective cognitive function, which is associated with a worse course of illness and poor functional outcomes. Nevertheless, the temporal progression of cognitive dysfunction in BD remains unclear and the identification of objective endophenotypes can inform the aetiology of BD.Methods:The present study is a cross-sectional investigation of cognitive baseline data from the longitudinal Bipolar Illness Onset-study. One hundred seventy-two remitted patients newly diagnosed with BD, 52 of their unaffected relatives (UR), and 110 healthy controls (HC) were compared on a large battery of behavioural cognitive tasks tapping into non-affective (i.e. neurocognitive) and affective (i.e. emotion processing and regulation) cognition.Results:Relative to HCs, patients with BD exhibited global neurocognitive deficits (ps < 0.001), as well as aberrant emotion processing and regulation (ps ⩽ 0.011); including decreased emotional reactivity to positive social scenarios, impaired ability to down-regulate positive emotion, as well as a specific deficit in the ability to recognise surprised facial expressions. Their URs also showed a trend towards difficulties identifying surprised faces (p = 0.075). No other differences in cognitive function were found for URs compared to HCs.Conclusions: Neurocognitive deficits and impairments within emotion processing and regulation may be illness-related deficits of BD that present after illness-onset, whereas processing of emotional faces may represent an early risk marker of BD. However, longitudinal studies are needed to examine the association between cognitive impairments and illness progression in BD. ",
keywords = "Affective cognition, bipolar disorder, emotion, endophenotypes, neurocognition regulation",
author = "Kj{\ae}rstad, {Hanne Lie} and Nicolaj Mistarz and Klara Coello and Sharleny Stanislaus and Melbye, {Sigurd Arne} and Harmer, {Catherine J.} and Maj Vinberg and Kamilla Miskowiak and Kessing, {Lars Vedel}",
year = "2020",
doi = "10.1017/S0033291719001867",
language = "English",
volume = "50",
pages = "1808--1819",
journal = "Psychological Medicine",
issn = "0033-2917",
publisher = "Cambridge University Press",
number = "11",

}

RIS

TY - JOUR

T1 - Aberrant cognition in newly diagnosed patients with bipolar disorder and their unaffected relatives

AU - Kjærstad, Hanne Lie

AU - Mistarz, Nicolaj

AU - Coello, Klara

AU - Stanislaus, Sharleny

AU - Melbye, Sigurd Arne

AU - Harmer, Catherine J.

AU - Vinberg, Maj

AU - Miskowiak, Kamilla

AU - Kessing, Lars Vedel

PY - 2020

Y1 - 2020

N2 - Background:Patients with bipolar disorder (BD) experience persistent impairments in both affective and non-affective cognitive function, which is associated with a worse course of illness and poor functional outcomes. Nevertheless, the temporal progression of cognitive dysfunction in BD remains unclear and the identification of objective endophenotypes can inform the aetiology of BD.Methods:The present study is a cross-sectional investigation of cognitive baseline data from the longitudinal Bipolar Illness Onset-study. One hundred seventy-two remitted patients newly diagnosed with BD, 52 of their unaffected relatives (UR), and 110 healthy controls (HC) were compared on a large battery of behavioural cognitive tasks tapping into non-affective (i.e. neurocognitive) and affective (i.e. emotion processing and regulation) cognition.Results:Relative to HCs, patients with BD exhibited global neurocognitive deficits (ps < 0.001), as well as aberrant emotion processing and regulation (ps ⩽ 0.011); including decreased emotional reactivity to positive social scenarios, impaired ability to down-regulate positive emotion, as well as a specific deficit in the ability to recognise surprised facial expressions. Their URs also showed a trend towards difficulties identifying surprised faces (p = 0.075). No other differences in cognitive function were found for URs compared to HCs.Conclusions: Neurocognitive deficits and impairments within emotion processing and regulation may be illness-related deficits of BD that present after illness-onset, whereas processing of emotional faces may represent an early risk marker of BD. However, longitudinal studies are needed to examine the association between cognitive impairments and illness progression in BD.

AB - Background:Patients with bipolar disorder (BD) experience persistent impairments in both affective and non-affective cognitive function, which is associated with a worse course of illness and poor functional outcomes. Nevertheless, the temporal progression of cognitive dysfunction in BD remains unclear and the identification of objective endophenotypes can inform the aetiology of BD.Methods:The present study is a cross-sectional investigation of cognitive baseline data from the longitudinal Bipolar Illness Onset-study. One hundred seventy-two remitted patients newly diagnosed with BD, 52 of their unaffected relatives (UR), and 110 healthy controls (HC) were compared on a large battery of behavioural cognitive tasks tapping into non-affective (i.e. neurocognitive) and affective (i.e. emotion processing and regulation) cognition.Results:Relative to HCs, patients with BD exhibited global neurocognitive deficits (ps < 0.001), as well as aberrant emotion processing and regulation (ps ⩽ 0.011); including decreased emotional reactivity to positive social scenarios, impaired ability to down-regulate positive emotion, as well as a specific deficit in the ability to recognise surprised facial expressions. Their URs also showed a trend towards difficulties identifying surprised faces (p = 0.075). No other differences in cognitive function were found for URs compared to HCs.Conclusions: Neurocognitive deficits and impairments within emotion processing and regulation may be illness-related deficits of BD that present after illness-onset, whereas processing of emotional faces may represent an early risk marker of BD. However, longitudinal studies are needed to examine the association between cognitive impairments and illness progression in BD.

KW - Affective cognition

KW - bipolar disorder

KW - emotion

KW - endophenotypes

KW - neurocognition regulation

U2 - 10.1017/S0033291719001867

DO - 10.1017/S0033291719001867

M3 - Journal article

C2 - 31456531

AN - SCOPUS:85071949960

VL - 50

SP - 1808

EP - 1819

JO - Psychological Medicine

JF - Psychological Medicine

SN - 0033-2917

IS - 11

ER -

ID: 240315393