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Validation of the predictive value of BDNF -87 methylation for antidepressant treatment success in severely depressed patients—a randomized rater-blinded trial

Authors :
Hannah Benedictine Maier
Alexandra Neyazi
Gabriel L. Bundies
Fiona Meyer-Bockenkamp
Stefan Bleich
Hansi Pathak
Yvonne Ziert
Barbara Neuhaus
Franz-Josef Müller
Iris Pollmann
Thomas Illig
Stefanie Mücke
Meike Müller
Brinja Kira Möller
Steffen Oeltze-Jafra
Tim Kacprowski
Jan Voges
Fabian Müntefering
Josef Scheiber
Andreas Reif
Mareike Aichholzer
Christine Reif-Leonhard
Maren Schmidt-Kassow
Ulrich Hegerl
Hanna Reich
Stefan Unterecker
Heike Weber
Jürgen Deckert
Nicole Bössel-Debbert
Hans J. Grabe
Michael Lucht
Helge Frieling
Source :
Trials, Vol 25, Iss 1, Pp 1-12 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Background Brain-derived neurotrophic factor (BDNF) is essential for antidepressant treatment of major depressive disorder (MDD). Our repeated studies suggest that DNA methylation of a specific CpG site in the promoter region of exon IV of the BDNF gene (CpG -87) might be predictive of the efficacy of monoaminergic antidepressants such as selective serotonin reuptake inhibitors (SSRIs), serotonin-norepinephrine reuptake inhibitors (SNRIs), and others. This trial aims to evaluate whether knowing the biomarker is non-inferior to treatment-as-usual (TAU) regarding remission rates while exhibiting significantly fewer adverse events (AE). Methods The BDNF trial is a prospective, randomized, rater-blinded diagnostic study conducted at five university hospitals in Germany. The study’s main hypothesis is that {1} knowing the methylation status of CpG -87 is non-inferior to not knowing it with respect to the remission rate while it significantly reduces the AE rate in patients experiencing at least one AE. The baseline assessment will occur upon hospitalization and a follow-up assessment on day 49 (± 3). A telephone follow-up will be conducted on day 70 (± 3). A total of 256 patients will be recruited, and methylation will be evaluated in all participants. They will be randomly assigned to either the marker or the TAU group. In the marker group, the methylation results will be shared with both the patient and their treating physician. In the TAU group, neither the patients nor their treating physicians will receive the marker status. The primary endpoints include the rate of patients achieving remission on day 49 (± 3), defined as a score of ≤ 10 on the Hamilton Depression Rating Scale (HDRS-24), and the occurrence of AE. Ethics and dissemination The trial protocol has received approval from the Institutional Review Boards at the five participating universities. This trial holds significance in generating valuable data on a predictive biomarker for antidepressant treatment in patients with MDD. The findings will be shared with study participants, disseminated through professional society meetings, and published in peer-reviewed journals. Trial registration German Clinical Trial Register DRKS00032503. Registered on 17 August 2023.

Details

Language :
English
ISSN :
17456215
Volume :
25
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
edsdoj.55ea2c6790ba48b2a005ed3270692acc
Document Type :
article
Full Text :
https://doi.org/10.1186/s13063-024-08061-5