When worry may be good for you: Worry severity and limbic-prefrontal functional connectivity in late-life generalized anxiety disorder.


Journal

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

Informations de publication

Date de publication:
01 10 2019
Historique:
received: 31 10 2018
revised: 31 05 2019
accepted: 04 07 2019
pubmed: 30 7 2019
medline: 26 6 2020
entrez: 30 7 2019
Statut: ppublish

Résumé

Late-life generalized anxiety disorder (GAD) is one of the most common anxiety disorders in older adults. However, its neural markers have received relatively little attention. In this study, we explored the association between worry severity and limbic-prefrontal connectivity during emotional reactivity in late-life GAD. We recruited 16 anxious (GAD) and 20 non-anxious (HC) older adults to perform the faces/shapes emotional reactivity task during functional magnetic resonance imaging (fMRI). We investigated the functional connectivity of both the amygdala and the bed nucleus of stria terminalis (BNST) with the prefrontal cortex (PFC) using generalized psychophysiological interaction (gPPI) analysis. We tested for (1) group differences in connectivity, (2) association between worry severity and connectivity, and (3) interaction between group and worry severity and its association with connectivity. Amygdala-PFC and BNST-PFC functional connectivity were associated with worry severity in an inverse U-shape, and was independent of depression severity, global anxiety, neuroticism, and general cognitive function. Our limitations include slightly skewed PSWQ distributions, lack of non-anxious individuals with high worry, small sample size, and low depression comorbidity in a sample of late-life GAD that may not generalize to GAD in younger populations. This suggests that moderate worry is associated with maximum engagement of the limbic-PFC connectivity, while severe worry is associated with failure of the limbic-PFC emotional regulation circuit. This may explain the aberrant and exaggerated responses to negative stimuli observed in participants with pathological worry.

Sections du résumé

BACKGROUND
Late-life generalized anxiety disorder (GAD) is one of the most common anxiety disorders in older adults. However, its neural markers have received relatively little attention. In this study, we explored the association between worry severity and limbic-prefrontal connectivity during emotional reactivity in late-life GAD.
METHODS
We recruited 16 anxious (GAD) and 20 non-anxious (HC) older adults to perform the faces/shapes emotional reactivity task during functional magnetic resonance imaging (fMRI). We investigated the functional connectivity of both the amygdala and the bed nucleus of stria terminalis (BNST) with the prefrontal cortex (PFC) using generalized psychophysiological interaction (gPPI) analysis. We tested for (1) group differences in connectivity, (2) association between worry severity and connectivity, and (3) interaction between group and worry severity and its association with connectivity.
RESULTS
Amygdala-PFC and BNST-PFC functional connectivity were associated with worry severity in an inverse U-shape, and was independent of depression severity, global anxiety, neuroticism, and general cognitive function.
LIMITATIONS
Our limitations include slightly skewed PSWQ distributions, lack of non-anxious individuals with high worry, small sample size, and low depression comorbidity in a sample of late-life GAD that may not generalize to GAD in younger populations.
CONCLUSIONS
This suggests that moderate worry is associated with maximum engagement of the limbic-PFC connectivity, while severe worry is associated with failure of the limbic-PFC emotional regulation circuit. This may explain the aberrant and exaggerated responses to negative stimuli observed in participants with pathological worry.

Identifiants

pubmed: 31357162
pii: S0165-0327(18)32786-1
doi: 10.1016/j.jad.2019.07.022
pmc: PMC6711791
mid: NIHMS1535659
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

650-657

Subventions

Organisme : NIMH NIH HHS
ID : K23 MH086686
Pays : United States
Organisme : NIMH NIH HHS
ID : P30 MH071944
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH108509
Pays : United States
Organisme : NIA NIH HHS
ID : T32 AG055381
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH076079
Pays : United States

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

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Auteurs

M Wu (M)

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

D S Mennin (DS)

Teachers College, Columbia University, New York City, NY, USA.

M Ly (M)

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

H T Karim (HT)

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

L Banihashemi (L)

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

D L Tudorascu (DL)

Department of Internal Medicine, Graduate School of Public health, Pittsburgh, PA, USA; Department of Biostatistics, Graduate School of Public Health, Pittsburgh, PA, USA.

H J Aizenstein (HJ)

Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.

C Andreescu (C)

Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. Electronic address: Andrcx@upmc.edu.

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