Impaired cognitive self-awareness mediates the association between alexithymia and excitation/inhibition balance in the pgACC.


Journal

Psychological medicine
ISSN: 1469-8978
Titre abrégé: Psychol Med
Pays: England
ID NLM: 1254142

Informations de publication

Date de publication:
07 2020
Historique:
pubmed: 23 7 2019
medline: 4 6 2021
entrez: 23 7 2019
Statut: ppublish

Résumé

Previous research showed that automatic emotion regulation is associated with activation of subcortical areas and subsequent feedforward processes to cortical areas. In contrast, cognitive awareness of emotions is mediated by negative feedback from cortical to subcortical areas. Pregenual anterior cingulate cortex (pgACC) is essential in the modulation of both affect and alexithymia. We considered the interplay between these two mechanisms in the pgACC and their relationship with alexithymia. In 68 healthy participants (30 women, age = 26.15 ± 4.22) we tested associations of emotion processing and alexithymia with excitation/inhibition (E/I) balance represented as glutamate (Glu)/GABA in the pgACC measured via magnetic resonance spectroscopy in 7 T. Alexithymia was positively correlated with the Glu/GABA ratio (N = 41, p = 0.0393). Further, cognitive self-awareness showed an association with Glu/GABA (N = 52, p = 0.003), which was driven by a correlation with GABA. In contrast, emotion regulation was only correlated with glutamate levels in the pgACC (N = 49, p = 0.008). Our results corroborate the importance of the pgACC as a mediating region of alexithymia, reflected in an altered E/I balance. Furthermore, we could specify that this altered balance is linked to a GABA-related modulation of cognitive self-awareness of emotions.

Sections du résumé

BACKGROUND
Previous research showed that automatic emotion regulation is associated with activation of subcortical areas and subsequent feedforward processes to cortical areas. In contrast, cognitive awareness of emotions is mediated by negative feedback from cortical to subcortical areas. Pregenual anterior cingulate cortex (pgACC) is essential in the modulation of both affect and alexithymia. We considered the interplay between these two mechanisms in the pgACC and their relationship with alexithymia.
METHOD
In 68 healthy participants (30 women, age = 26.15 ± 4.22) we tested associations of emotion processing and alexithymia with excitation/inhibition (E/I) balance represented as glutamate (Glu)/GABA in the pgACC measured via magnetic resonance spectroscopy in 7 T.
RESULTS
Alexithymia was positively correlated with the Glu/GABA ratio (N = 41, p = 0.0393). Further, cognitive self-awareness showed an association with Glu/GABA (N = 52, p = 0.003), which was driven by a correlation with GABA. In contrast, emotion regulation was only correlated with glutamate levels in the pgACC (N = 49, p = 0.008).
CONCLUSION
Our results corroborate the importance of the pgACC as a mediating region of alexithymia, reflected in an altered E/I balance. Furthermore, we could specify that this altered balance is linked to a GABA-related modulation of cognitive self-awareness of emotions.

Identifiants

pubmed: 31328716
pii: S0033291719001806
doi: 10.1017/S0033291719001806
doi:

Substances chimiques

Glutamic Acid 3KX376GY7L
gamma-Aminobutyric Acid 56-12-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1727-1735

Auteurs

A Kühnel (A)

Clinical Affective Neuroimaging Laboratory, Magdeburg, Germany.
Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry and International Max Planck Research School for Translational Psychiatry (IMPRS-TP), Munich, Germany.

A Widmann (A)

Clinical Affective Neuroimaging Laboratory, Magdeburg, Germany.
University Department of Psychiatry and Psychotherapy, University Tübingen, Tübingen, Germany.
Experimental and Molecular Psychiatry, LWL University Hospital, Ruhr University Bochum, Bochum, Germany.

L Colic (L)

Clinical Affective Neuroimaging Laboratory, Magdeburg, Germany.
Leibniz Institute for Neurobiology, Magdeburg, Germany.
Department of Psychiatry, Mood Disorders Research Program, Yale School of Medicine, New Haven, CT, USA.

L Herrmann (L)

University Department of Psychiatry and Psychotherapy, University Tübingen, Tübingen, Germany.

L R Demenescu (LR)

Clinical Affective Neuroimaging Laboratory, Magdeburg, Germany.

A L Leutritz (AL)

Clinical Affective Neuroimaging Laboratory, Magdeburg, Germany.

M Li (M)

University Department of Psychiatry and Psychotherapy, University Tübingen, Tübingen, Germany.
Department of Psychiatry and Psychotherapy, OVGU Magdeburg, Magdeburg, Germany.

S Grimm (S)

Department of Psychiatry, Charité, CBF, Berlin, Germany.
MSB Medical School Berlin, Calandrellistraße 1-9, 12247Berlin, Germany.
Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital, University of Zurich, 8032Zurich, Switzerland.

T Nolte (T)

The Anna Freud National Centre for Children and Families, London, UK.
Wellcome Trust Centre for Neuroimaging, University College London, London, UK.

P Fonagy (P)

The Anna Freud National Centre for Children and Families, London, UK.
Research Department of Clinical, Educational and Health Psychology, University College London, London, UK.

M Walter (M)

Clinical Affective Neuroimaging Laboratory, Magdeburg, Germany.
University Department of Psychiatry and Psychotherapy, University Tübingen, Tübingen, Germany.
Leibniz Institute for Neurobiology, Magdeburg, Germany.
Center for Behavioral Brain Sciences (CBBS), Magdeburg, Germany.
Max Planck Institute for Biological Cybernetics, Tübingen, Germany.

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Classifications MeSH