Evidence map›Paper›PMID 30104601›Full record

ArticleTranslational psychiatry2018

Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP).

Hongyan Ren, Chiara Fabbri, Rudolf Uher, Marcella Rietschel, Ole Mors, Neven Henigsberg, Joanna Hauser, Astrid Zobel, Wolfgang Maier, Mojca Z Dernovsek and 8 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 19% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
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  7. Understanding Anhedonia from a Genomic Perspective.Current topics in behavioral neurosciences · 2022
    Review
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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

18 authors at 10 institutions in 8 countries.

Hongyan RenPsychiatry and Medical Genetics, University of Alberta, Edmonton, AB, Canada.
Chiara FabbriMRC Social, Genetic and Developmental Psychiatry Centre, King's College London, London, UK.
Rudolf UherPsychiatry Department, Dalhousie University, Halifax, NS, Canada.
Marcella RietschelDivision of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Mannheim, Germany.ORCID http://orcid.org/0000-0002-5236-6149
Ole MorsClinical Medicine, Aarhus University, Aarhus, Denmark.
Neven HenigsbergCroatian Institute for Brain Research, University of Zagreb, Zagreb, Croatia.ORCID http://orcid.org/0000-0002-5303-1834
Joanna HauserPsychiatry Department, University of Poznan, Poznan, Poland.
Astrid ZobelPsychiatry Department, University of Bonn, Bonn, Germany.
Wolfgang MaierPsychiatry Department, University of Bonn, Bonn, Germany.
Mojca Z DernovsekUniversity Psychiatric Clinic, University of Ljubliana, Ljubljana, Slovenia.
Daniel SoueryPsychological Medicine, Free University of Brussels, Brussels, Belgium.
Annamaria CattaneoIRCCS, University of Brescia, Brescia, Italy.
Gerome BreenMRC Social, Genetic and Developmental Psychiatry Centre, King's College London, London, UK.
Ian W CraigMRC Social, Genetic and Developmental Psychiatry Centre, King's College London, London, UK.
Anne E FarmerMRC Social, Genetic and Developmental Psychiatry Centre, King's College London, London, UK.
Peter McGuffinMRC Social, Genetic and Developmental Psychiatry Centre, King's College London, London, UK.
Cathryn M LewisMRC Social, Genetic and Developmental Psychiatry Centre, King's College London, London, UK.ORCID http://orcid.org/0000-0002-8249-8476
Katherine J AitchisonPsychiatry and Medical Genetics, University of Alberta, Edmonton, AB, Canada. kaitchis@ualberta.ca.ORCID http://orcid.org/0000-0002-1107-3024
King's College London · GBUniversity of Alberta · CAUniversity of Bonn · DEAarhus University · DKCentral Institute of Mental Health · DEDalhousie University · CAPoznań University of Technology · PLUniversity of Brescia · ITUniversity of Zagreb · HRUniversity Psychiatric Hospital · SI

Funding

Department of Health
6 · The paper itself

Abstract

A key feature of major depressive disorder (MDD) is anhedonia, which is a predictor of response to antidepressant treatment. In order to shed light on its genetic underpinnings, we conducted a genome-wide association study (GWAS) followed by investigation of biological pathway enrichment using an anhedonia dimension for 759 patients with MDD in the GENDEP study. The GWAS identified 18 SNPs associated at genome-wide significance with the top one being an intronic SNP (rs9392549) in PRPF4B (pre-mRNA processing factor 4B) located on chromosome 6 (P = 2.07 × 10

Indexed as

AnhedoniaAdultFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyGray MatterHumansMajor Depressive DisorderMaleMiddle AgedMultifactorial InheritanceNucleus AccumbensPolymorphism, Single NucleotideProtein Serine-Threonine KinasesRegression AnalysisRibonucleoprotein, U4-U6 Small NuclearProtein Serine-Threonine KinasesPRPF4B protein, humanRibonucleoprotein, U4-U6 Small Nuclear

Identifiers

PMID30104601
PMCPMC6089928
OpenAlexW2885300986

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.