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Executive functions and borderline personality features in adolescents with major depressive disorder

BACKGROUND: Executive functions (EF) consolidate during adolescence and are impaired in various emerging psychiatric disorders, such as pediatric Major Depressive Disorder (pMDD) and Borderline Personality Disorder. Previous studies point to a marked heterogeneity of deficits in EF in pMDD. We exami...

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Autores principales: Albermann, Mona, Emery, Sophie, Baumgartner, Noemi, Strumberger, Michael, Erb, Suzanne, Wöckel, Lars, Müller-Knapp, Ulrich, Rhiner, Bruno, Contin-Waldvogel, Brigitte, Bachmann, Silke, Schmeck, Klaus, Berger, Gregor, Häberling, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325791/
https://www.ncbi.nlm.nih.gov/pubmed/37425294
http://dx.doi.org/10.3389/fnhum.2023.957753
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author Albermann, Mona
Emery, Sophie
Baumgartner, Noemi
Strumberger, Michael
Erb, Suzanne
Wöckel, Lars
Müller-Knapp, Ulrich
Rhiner, Bruno
Contin-Waldvogel, Brigitte
Bachmann, Silke
Schmeck, Klaus
Berger, Gregor
Häberling, Isabelle
author_facet Albermann, Mona
Emery, Sophie
Baumgartner, Noemi
Strumberger, Michael
Erb, Suzanne
Wöckel, Lars
Müller-Knapp, Ulrich
Rhiner, Bruno
Contin-Waldvogel, Brigitte
Bachmann, Silke
Schmeck, Klaus
Berger, Gregor
Häberling, Isabelle
author_sort Albermann, Mona
collection PubMed
description BACKGROUND: Executive functions (EF) consolidate during adolescence and are impaired in various emerging psychiatric disorders, such as pediatric Major Depressive Disorder (pMDD) and Borderline Personality Disorder. Previous studies point to a marked heterogeneity of deficits in EF in pMDD. We examined the hypothesis that deficits in EF in adolescents with pMDD might be related to comorbid Borderline Personality features (BPF). METHODS: We examined a sample of 144 adolescents (15.86 ± 1.32) diagnosed with pMDD. Parents rated their child’s EF in everyday life with the Behavior Rating Inventory of Executive Function (BRIEF) and BPF with the Impulsivity and Emotion Dysregulation Scale (IED-27). The adolescents completed equivalent self-rating measures. Self- and parent-ratings of the BRIEF scores were compared with paired t-Tests. Correlation and parallel mediation analyses, ICC, and multiple regression analyses were used to assess symptom overlap, parent-child agreement, and the influence of depression severity. RESULTS: Over the whole sample, none of the self- or parent-rated BRIEF scales reached a mean score above T > 65, which would indicate clinically impaired functioning. Adolescents tended to report higher impairment in EF than their parents. Depression severity was the strongest predictor for BPF scores, with Emotional Control predicting parent-rated BPF and Inhibit predicting self-rated BPF. Furthermore, the Behavioral Regulation Index, which includes EF closely related to behavioral control, significantly mediated the relationship between depression severity and IED-27 factors emotional dysregulation and relationship difficulties but not non-suicidal self-injuries. CONCLUSION: On average, adolescents with depression show only subtle deficits in executive functioning. However, increased EF deficits are associated with the occurrence of comorbid borderline personality features, contributing to a more severe overall psychopathology. Therefore, training of executive functioning might have a positive effect on psychosocial functioning in severely depressed adolescents, as it might also improve comorbid BPF. CLINICAL TRIAL REGISTRATION: www.ClinicalTrials.gov, identifier NCT03167307.
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spelling pubmed-103257912023-07-07 Executive functions and borderline personality features in adolescents with major depressive disorder Albermann, Mona Emery, Sophie Baumgartner, Noemi Strumberger, Michael Erb, Suzanne Wöckel, Lars Müller-Knapp, Ulrich Rhiner, Bruno Contin-Waldvogel, Brigitte Bachmann, Silke Schmeck, Klaus Berger, Gregor Häberling, Isabelle Front Hum Neurosci Neuroscience BACKGROUND: Executive functions (EF) consolidate during adolescence and are impaired in various emerging psychiatric disorders, such as pediatric Major Depressive Disorder (pMDD) and Borderline Personality Disorder. Previous studies point to a marked heterogeneity of deficits in EF in pMDD. We examined the hypothesis that deficits in EF in adolescents with pMDD might be related to comorbid Borderline Personality features (BPF). METHODS: We examined a sample of 144 adolescents (15.86 ± 1.32) diagnosed with pMDD. Parents rated their child’s EF in everyday life with the Behavior Rating Inventory of Executive Function (BRIEF) and BPF with the Impulsivity and Emotion Dysregulation Scale (IED-27). The adolescents completed equivalent self-rating measures. Self- and parent-ratings of the BRIEF scores were compared with paired t-Tests. Correlation and parallel mediation analyses, ICC, and multiple regression analyses were used to assess symptom overlap, parent-child agreement, and the influence of depression severity. RESULTS: Over the whole sample, none of the self- or parent-rated BRIEF scales reached a mean score above T > 65, which would indicate clinically impaired functioning. Adolescents tended to report higher impairment in EF than their parents. Depression severity was the strongest predictor for BPF scores, with Emotional Control predicting parent-rated BPF and Inhibit predicting self-rated BPF. Furthermore, the Behavioral Regulation Index, which includes EF closely related to behavioral control, significantly mediated the relationship between depression severity and IED-27 factors emotional dysregulation and relationship difficulties but not non-suicidal self-injuries. CONCLUSION: On average, adolescents with depression show only subtle deficits in executive functioning. However, increased EF deficits are associated with the occurrence of comorbid borderline personality features, contributing to a more severe overall psychopathology. Therefore, training of executive functioning might have a positive effect on psychosocial functioning in severely depressed adolescents, as it might also improve comorbid BPF. CLINICAL TRIAL REGISTRATION: www.ClinicalTrials.gov, identifier NCT03167307. Frontiers Media S.A. 2023-06-22 /pmc/articles/PMC10325791/ /pubmed/37425294 http://dx.doi.org/10.3389/fnhum.2023.957753 Text en Copyright © 2023 Albermann, Emery, Baumgartner, Strumberger, Erb, Wöckel, Müller-Knapp, Rhiner, Contin-Waldvogel, Bachmann, Schmeck, Berger, the Omega-3 Study Team and Häberling. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Albermann, Mona
Emery, Sophie
Baumgartner, Noemi
Strumberger, Michael
Erb, Suzanne
Wöckel, Lars
Müller-Knapp, Ulrich
Rhiner, Bruno
Contin-Waldvogel, Brigitte
Bachmann, Silke
Schmeck, Klaus
Berger, Gregor
Häberling, Isabelle
Executive functions and borderline personality features in adolescents with major depressive disorder
title Executive functions and borderline personality features in adolescents with major depressive disorder
title_full Executive functions and borderline personality features in adolescents with major depressive disorder
title_fullStr Executive functions and borderline personality features in adolescents with major depressive disorder
title_full_unstemmed Executive functions and borderline personality features in adolescents with major depressive disorder
title_short Executive functions and borderline personality features in adolescents with major depressive disorder
title_sort executive functions and borderline personality features in adolescents with major depressive disorder
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325791/
https://www.ncbi.nlm.nih.gov/pubmed/37425294
http://dx.doi.org/10.3389/fnhum.2023.957753
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