FKBP5 Gene Expression Predicts Antidepressant Treatment Outcome in Depression.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
23 Jan 2019
Historique:
received: 09 12 2018
revised: 13 01 2019
accepted: 20 01 2019
entrez: 26 1 2019
pubmed: 27 1 2019
medline: 10 5 2019
Statut: epublish

Résumé

Adverse experiences and chronic stress are well-known risk factors for the development of major depression, and an impaired stress response regulation is frequently observed in acute depression. Impaired glucocorticoid receptor (GR) signalling plays an important role in these alterations, and a restoration of GR signalling appears to be a prerequisite of successful antidepressant treatment. Variants in genes of the stress response regulation contribute to the vulnerability to depression in traumatized subjects. Consistent findings point to an important role of FKBP5, the gene expressing FK506-binding protein 51 (FKBP51), which is a strong inhibitor of the GR, and thus, an important regulator of the stress response. We investigated the role of FKBP5 and FKB51 expression with respect to stress response regulation and antidepressant treatment outcome in depressed patients. This study included 297 inpatients, who participated in the Munich Antidepressant Response Signature (MARS) project and were treated for acute depression. In this open-label study, patients received antidepressant treatment according to the attending doctor's choice. In addition to the

Identifiants

pubmed: 30678080
pii: ijms20030485
doi: 10.3390/ijms20030485
pmc: PMC6387218
pii:
doi:

Substances chimiques

Antidepressive Agents 0
Biomarkers 0
Tacrolimus Binding Proteins EC 5.2.1.-
tacrolimus binding protein 5 EC 5.2.1.8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Bundesministerium für Bildung und Forschung
ID : 01ES0811

Déclaration de conflit d'intérêts

The authors F.H. and M.U are coinventors of the patent “FKBP51: a novel target for antidepressant therapy” (WO2005054500). All other authors declare no conflict of interest.

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Auteurs

Marcus Ising (M)

Max Planck Institute of Psychiatry, 80804 Munich, Germany. ising@psych.mpg.de.

Giuseppina Maccarrone (G)

Max Planck Institute of Psychiatry, 80804 Munich, Germany. maccarrone@psych.mpg.de.

Tanja Brückl (T)

Max Planck Institute of Psychiatry, 80804 Munich, Germany. brueckl@psych.mpg.de.

Sandra Scheuer (S)

Max Planck Institute of Psychiatry, 80804 Munich, Germany. scheuer.sandra@gmail.com.

Johannes Hennings (J)

kbo-Isar-Amper Clinical Center Munich East, 85540 Munich, Germany. johannes.hennings@kbo.de.

Florian Holsboer (F)

Max Planck Institute of Psychiatry, 80804 Munich, Germany. florian.holsboer@hmnc.de.
HMNC Brain Health GmbH, 80807 Munich, Germany. florian.holsboer@hmnc.de.

Christoph W Turck (CW)

Max Planck Institute of Psychiatry, 80804 Munich, Germany. turck@psych.mpg.de.

Manfred Uhr (M)

Max Planck Institute of Psychiatry, 80804 Munich, Germany. uhr@psych.mpg.de.

Susanne Lucae (S)

Max Planck Institute of Psychiatry, 80804 Munich, Germany. ising@psych.mpg.de.

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