Stable neural underpinnings of emotional cognition subgroups in patients newly diagnosed with bipolar disorder: A prospective fMRI study

Author:

Kjærstad Hanne Lie12ORCID,de Siqueira Rotenberg Luisa3ORCID,Macoveanu Julian12ORCID,Coello Klara2ORCID,Faurholt‐Jepsen Maria24,Bjertrup Anne Juul12,Knudsen Gitte M.45,Fisher Patrick M.56,Vinberg Maj247ORCID,Kessing Lars Vedel24ORCID,Lafer Beny3,Miskowiak Kamilla Woznica12

Affiliation:

1. Neurocognition and Emotion in Affective Disorders (NEAD) Centre, Psychiatric Centre Copenhagen, Mental Health Services, Capital Region of Denmark, and Department of Psychology University of Copenhagen Copenhagen Denmark

2. Copenhagen Affective Disorder Research Centre (CADIC), Psychiatric Centre Copenhagen, Frederiksberg Hospital Frederiksberg Denmark

3. Bipolar Disorder Program (PROMAN), Department of Psychiatry University of São Paulo Medical School São Paulo Brazil

4. Department of Clinical Medicine University of Copenhagen Copenhagen Denmark

5. Neurobiology Research Unit Copenhagen University Hospital Rigshospitalet Denmark

6. Department of Drug Design and Pharmacology University of Copenhagen Copenhagen Denmark

7. Mental Health Center, Northern Zealand Copenhagen University Hospital – Mental Health Services CPH Copenhagen Denmark

Abstract

AbstractObjectivesThis study aimed to investigate the neural underpinnings of emotional cognition subgroups in recently diagnosed patients with bipolar disorder (BD) and change over time over a 15‐month follow‐up period.MethodsPatients and healthy controls (HC) underwent emotional and nonemotional cognitive assessments and functional magnetic resonance imaging (fMRI) at the baseline (BD n = 87; HC n = 65) and at 15‐month follow‐up (BD n = 44; HC n = 38). Neural activity during emotion reactivity and regulation in response to aversive pictures was assessed during fMRI. Patients were clustered into subgroups based on their emotional cognition and, with HC, were compared longitudinally on cognition and neural activity during emotion reactivity and regulation.ResultsPatients were optimally clustered into two subgroups: Subgroup 1 (n = 40, 46%) was characterized by heightened emotional reactivity in negative social scenarios, which persisted over time, but were otherwise cognitively intact. This subgroup exhibited stable left amygdala hyper‐activity over time during emotion reactivity compared to subgroup 2. Subgroup 2 (n = 47, 54%) was characterized by global emotional cognitive impairments, including stable difficulties with emotion regulation over time. During emotion regulation across both time points, this group exhibited hypo‐activity in the left dorsolateral prefrontal cortex. Additionally, patients in subgroup 2 had poorer nonemotional cognition, had more psychiatric hospital admissions and history of psychotic episodes than those in subgroup 1.ConclusionsBroad impairments in emotional cognition in approximately half of BD patients and associated nonemotional cognitive deficits may originate from insufficient recruitment of prefrontal resources, contributing to poorer clinical outcomes.

Funder

Augustinus Fonden

Copenhagen Center for Health Technology

Innovationsfonden

Helsefonden

Gangstedfonden

Markedsmodningsfonden

Danmarks Frie Forskningsfond

Region Hovedstadens Psykiatri

Publisher

Wiley

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