Literature DB >> 27379618

Executive function deficits associated with current and past major depressive symptoms.

Keith Bredemeier1, Stacie L Warren2, Howard Berenbaum3, Gregory A Miller4, Wendy Heller3.   

Abstract

BACKGROUND: Although there has been extensive research showing that depression is associated with executive function (EF) deficits, the nature of these deficits is not clearly delineated. Specifically, previous reviews on this topic have yielded different conclusions about the particular domains of EF that are disrupted in depressed individuals. Further, research on whether these deficits persist after depressed mood has remitted is less prevalent and not consistent.
METHODS: In two independent samples of college students, we examined associations between clinical ratings of current and past symptoms of a Major Depressive Episode (MDE) and difficulties in two domains of EF: inhibition and shifting. In Study 1 (n=162), EF was measured using behavioral tasks shown to index these two domains. In Study 2 (n=95), EF was measured using a self-report questionnaire believed to capture EF difficulties experienced in daily life.
RESULTS: In both studies, past MDE symptoms were associated with worse shifting. In contrast, current MDE symptoms were associated with worse inhibition, though only on the behavioral measure (in Study 1). LIMITATIONS: Both studies used college samples and retrospective assessments of past symptoms. Further, only two domains of EF were examined, and the EF measures employed in each study have their own unique methodological limitations.
CONCLUSIONS: Findings suggest that inhibition deficits vary as a function of current symptoms and thus may be a by-product of distress rather than a causal contributor. In contrast, shifting deficits associated with depression appear to be more enduring, suggesting that they could contribute to risk for depression.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Depression; Executive function; Inhibition; Mood; Shifting

Mesh:

Year:  2016        PMID: 27379618      PMCID: PMC5064806          DOI: 10.1016/j.jad.2016.03.070

Source DB:  PubMed          Journal:  J Affect Disord        ISSN: 0165-0327            Impact factor:   4.839


  59 in total

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