Bipolar disorder;
high-risk subjects;
emotion processing;
face affect;
endophenotype;
FACIAL EMOTION;
SOCIAL COGNITION;
RECOGNITION;
FACE;
PERCEPTION;
CHILDREN;
DISGUST;
RISK;
D O I:
10.1177/02537176211026795
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
Background: Emotion processing deficits have been described in patients with bipolar disorder (BD) and are considered one of the core cognitive abnormalities in BD with endophenotype potential. However, the literature on specific impairments in emotion processing cognitive strategies (directive/cortical/higher versus intuitive/limbic/lower) in euthymic adult BD patients and healthy first-degree relatives/high-risk (HR) subjects in comparison with healthy controls (HCs) is sparse. Methods: We examined facial emotion recognition deficits (FERD) in BD (N = 30), HR (N = 21), and HC (N = 30) matched for age (years), years of education, and sex using computer-administered face emotions-Matching And Labeling Task (eMALT). Results: The three groups were significantly different based on labeling accuracy scores for fear and anger (FA) (P < 0.001) and sad and disgust (SD) (P < 0.001). On post-hoc analysis, HR subjects exhibited a significant deficit in the labeling accuracy of FA facial emotions (P < 0.001) compared to HC. The BD group was found to have significant differences in all FA (P = 0.004) and SD (P = 0.003) emotion matching as well as FA (P = 0.001) and SD (P < 0.001) emotion labeling accuracy scores. Conclusions: BD in remission exhibits FERD in general, whereas specific labeling deficits of fear and anger emotions, indicating impaired directive higher order aspect of emotion processing, were demonstrated in HR subjects. This appears to be a potential endophenotype. These deficits could underlie the pathogenesis in BD, with possible frontolimbic circuitry impairment. They may have potential implications in functional recovery and prognosis of BD.
机构:
Univ Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USAUniv Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
Njau, Stephanie
Townsend, Jennifer
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Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, 300 Med Plaza,Suite 2200, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
Townsend, Jennifer
Wade, Benjamin
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Univ Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USAUniv Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
Wade, Benjamin
Hellemann, Gerhard
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机构:
Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, 300 Med Plaza,Suite 2200, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
Hellemann, Gerhard
Bookheimer, Susan
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机构:
Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, 300 Med Plaza,Suite 2200, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
Bookheimer, Susan
Narr, Katherine
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机构:
Univ Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, 300 Med Plaza,Suite 2200, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
Narr, Katherine
Brooks, John O., III
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机构:
Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, 300 Med Plaza,Suite 2200, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Neurol, Geffen Sch Med, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA