White matter - emotion processing activity relationships in youth offspring of bipolar parents.


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
15 01 2019
Historique:
received: 09 03 2018
revised: 31 07 2018
accepted: 09 09 2018
pubmed: 23 9 2018
medline: 1 3 2019
entrez: 23 9 2018
Statut: ppublish

Résumé

Early detection of Bipolar Disorder (BD) is critical for targeting interventions to delay or prevent illness onset. Yet, the absence of objective BD biomarkers makes accurately identifying at-risk youth difficult. In this study, we examined how relationships between white matter tract (WMT) structure and activity in emotion processing neural circuitry differentiate youth at risk for BD from youth at risk for other psychiatric disorders. Offspring (ages 8-17) of parents with BD (OBP, n = 32), offspring of comparison parents with non-BD psychopathology (OCP, n = 30), and offspring of healthy parents (OHP, n = 24) underwent diffusion tensor and functional magnetic resonance imaging while performing an emotional face processing task. Penalized and multiple regression analyses included GROUP(OBP,OCP)xWMT interactions as main independent variables, and emotion processing activity as dependent variables, to determine significant group differences in WMT-activity relationships. 8 GROUPxWMT interaction variables contributed to 16.5% of the variance in amygdala and prefrontal cortical activity to happy faces. Of these, significant group differences in slopes (inverse for OBP, positive for OCP) existed for the relationship between forceps minor radial diffusivity and rostral anterior cingulate activity (p = 0.014). Slopes remained significantly different in unmedicated youth without psychiatric disorders (p = 0.017) and were moderated by affective lability symptoms (F(1,29) = 5.566, p = 0.036). Relatively small sample sizes were included. Forceps minor radial diffusivity-rostral anterior cingulate activity relationships may reflect underlying neuropathological processes that contribute to affectively labile youth at risk for BD and may help differentiate them from youth at risk for other psychiatric disorders.

Sections du résumé

BACKGROUND
Early detection of Bipolar Disorder (BD) is critical for targeting interventions to delay or prevent illness onset. Yet, the absence of objective BD biomarkers makes accurately identifying at-risk youth difficult. In this study, we examined how relationships between white matter tract (WMT) structure and activity in emotion processing neural circuitry differentiate youth at risk for BD from youth at risk for other psychiatric disorders.
METHODS
Offspring (ages 8-17) of parents with BD (OBP, n = 32), offspring of comparison parents with non-BD psychopathology (OCP, n = 30), and offspring of healthy parents (OHP, n = 24) underwent diffusion tensor and functional magnetic resonance imaging while performing an emotional face processing task. Penalized and multiple regression analyses included GROUP(OBP,OCP)xWMT interactions as main independent variables, and emotion processing activity as dependent variables, to determine significant group differences in WMT-activity relationships.
RESULTS
8 GROUPxWMT interaction variables contributed to 16.5% of the variance in amygdala and prefrontal cortical activity to happy faces. Of these, significant group differences in slopes (inverse for OBP, positive for OCP) existed for the relationship between forceps minor radial diffusivity and rostral anterior cingulate activity (p = 0.014). Slopes remained significantly different in unmedicated youth without psychiatric disorders (p = 0.017) and were moderated by affective lability symptoms (F(1,29) = 5.566, p = 0.036).
LIMITATIONS
Relatively small sample sizes were included.
CONCLUSIONS
Forceps minor radial diffusivity-rostral anterior cingulate activity relationships may reflect underlying neuropathological processes that contribute to affectively labile youth at risk for BD and may help differentiate them from youth at risk for other psychiatric disorders.

Identifiants

pubmed: 30243195
pii: S0165-0327(18)30361-6
doi: 10.1016/j.jad.2018.09.010
pmc: PMC6476540
mid: NIHMS1022719
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

153-164

Subventions

Organisme : NIMH NIH HHS
ID : F30 MH111102
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH060952
Pays : United States
Organisme : NCATS NIH HHS
ID : TL1 TR001858
Pays : United States

Informations de copyright

Copyright © 2018. Published by Elsevier B.V.

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Auteurs

Heather E Acuff (HE)

Departments of Neuroscience, Psychology, and Psychiatry, Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, USA; Medical Scientist Training Program, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. Electronic address: hea19@pitt.edu.

Amelia Versace (A)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Michele A Bertocci (MA)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Lindsay C Hanford (LC)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Cecile D Ladouceur (CD)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Anna Manelis (A)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Kelly Monk (K)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Lisa Bonar (L)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Alicia McCaffrey (A)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Benjamin I Goldstein (BI)

Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.

Tina R Goldstein (TR)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Dara Sakolsky (D)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

David Axelson (D)

Department of Psychiatry, Nationwide Children's Hospital and The Ohio State College of Medicine, Columbus, OH, USA.

Boris Birmaher (B)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Mary L Phillips (ML)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

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