Evidence map›Paper›PMID 30929060›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2020

Higher BDNF plasma levels are associated with a normalization of memory dysfunctions during an antidepressant treatment.

Jan Engelmann, Stefanie Wagner, Daniel Wollschläger, Sabine Kaaden, Konrad F Schlicht, Nadine Dreimüller, Dieter F Braus, Marianne B Müller, Oliver Tüscher, Helge Frieling and 2 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00974155 (Randomised Clinical Trial Comparing Early Medication Change), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00974155 phase4completednot on this map

Randomised Clinical Trial Comparing Early Medication Change (EMC) Strategy With Treatment as Usual (TAU) in Patients With Major Depressive Disorder - the EMC Trial

TypeinterventionalSponsorK. LiebRan2009 to 2014Enrolled889ConditionsDepressionArmsEscitalopram, venlafaxine, lithium, Escitalopram, venlafaxine
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Jan EngelmannDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes-Gutenberg-University Mainz, Untere Zahlbacher Straße 8, 55131, Mainz, Germany. jan.engelmann@unimedizin-mainz.de.ORCID http://orcid.org/0000-0001-8818-0138
Stefanie WagnerDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes-Gutenberg-University Mainz, Untere Zahlbacher Straße 8, 55131, Mainz, Germany.
Daniel WollschlägerInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center, Mainz, Germany.
Sabine KaadenDepartment of Psychiatry and Psychotherapy, HELIOS Dr. Horst-Schmidt-Kliniken, Wiesbaden, Germany.
Konrad F SchlichtDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes-Gutenberg-University Mainz, Untere Zahlbacher Straße 8, 55131, Mainz, Germany.
Nadine DreimüllerDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes-Gutenberg-University Mainz, Untere Zahlbacher Straße 8, 55131, Mainz, Germany.
Dieter F BrausDepartment of Psychiatry and Psychotherapy, HELIOS Dr. Horst-Schmidt-Kliniken, Wiesbaden, Germany.
Marianne B MüllerExperimental Psychiatry, Department of Psychiatry and Psychotherapy and Focus Program Translational Neuroscience, University Medical Center, Mainz, Germany.
Oliver TüscherDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes-Gutenberg-University Mainz, Untere Zahlbacher Straße 8, 55131, Mainz, Germany.
Helge FrielingMolecular Neuroscience Laboratory, Department of Psychiatry, Social Psychiatry and Psychotherapy, Medical School, Hannover, Germany.
André TadićDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes-Gutenberg-University Mainz, Untere Zahlbacher Straße 8, 55131, Mainz, Germany.
Klaus LiebDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes-Gutenberg-University Mainz, Untere Zahlbacher Straße 8, 55131, Mainz, Germany.
Johannes Gutenberg University Mainz · DEHelios Dr. Horst Schmidt Kliniken Wiesbaden · DEMedizinische Hochschule Hannover · DE

Funding

Bundesministerium für Bildung und Forschung BMBF grant n°: 01 KG 0906
6 · The paper itself

Abstract

One important symptom of patients with major depressive disorder (MDD) is memory dysfunction. However, little is known about the relationship between memory performance and depression severity, about the course of memory performance during antidepressant treatment as well as about the relationship between memory performance and brain-derived neurotrophic factor (BDNF). Memory function [learning and delayed recall) was assessed in 173 MDD patients (mean age 39.7 ± 11.3 years] treated by a pre-defined treatment algorithm within the early medication change (EMC) study at baseline, days 28 and 56. Depression severity was assessed in weekly intervals, BDNF plasma levels were measured at baseline, days 14 and 56, BDNF exon IV and p11 methylation status at baseline. Linear mixed regression models revealed that the course of depression severity was not associated with the course of learning or delayed recall in the total group. 63 (36%) of the investigated patients showed memory deficits (percent range ≤ 16) at baseline. Of those, 26(41%) patients experienced a normalization of their memory deficits during treatment. Patients with a normalization of their delayed recall performance had significantly higher plasma BDNF levels (p = 0.040) from baseline to day 56 than patients with persistent deficits. Baseline BDNF exon IV promoter and p11 gene methylation status were not associated with memory performance. Our results corroborate a concomitant amelioration of learning and delayed recall dysfunctions with successful antidepressant therapy in a subgroup of patients and support a role of BDNF in the neural mechanisms underlying the normalization of memory dysfunctions in MDD. ClinicalTrials.gov number: NCT00974155; EudraCT: 2008-008280-96.

Indexed as

Outcome Assessment, Health CareAdultAntidepressive AgentsBrain-Derived Neurotrophic FactorFemaleHumansMajor Depressive DisorderMaleMemory DisordersMental RecallMiddle AgedAntidepressive AgentsBDNF protein, humanBrain-Derived Neurotrophic FactorAntidepressant therapyBDNF exon IV and p11 promoter methylationBrain-derived neurotrophic factorMajor depressive disorderMemory

Identifiers

PMID30929060
OpenAlexW2935142044

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.