Evidence map›Paper›PMID 30700811›Full record

SynthesisThe pharmacogenomics journal2020

Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP.

Eleanor M Wigmore, Jonathan D Hafferty, Lynsey S Hall, David M Howard, Toni-Kim Clarke, Chiara Fabbri, Cathryn M Lewis, Rudolf Uher, Lauren B Navrady, Mark J Adams and 14 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in The pharmacogenomics journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 4 pooled it
6.8field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 4 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Article
  7. Article
  8. Comparative polygenic predispositions of treatment-resistant depression in East Asian and European populations.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  9. Article
  10. Cognition in Treatment-Resistant Depression: Obstacles and Challenges?Advances in experimental medicine and biology · 2026
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Genetic determinants of antidepressant and antipsychotic drug response.European archives of psychiatry and clinical neuroscience · 2025
    Article
  17. Article
  18. Article
  19. Review
  20. 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

24 authors at 10 institutions in 5 countries.

Eleanor M WigmoreDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK. eleanor.wigmore@astrazeneca.com.ORCID http://orcid.org/0000-0003-0864-9990
Jonathan D HaffertyDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK.
Lynsey S HallDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK.
David M HowardDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK.
Toni-Kim ClarkeDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK.
Chiara FabbriMRC SGDP Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, England.
Cathryn M LewisMRC SGDP Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, England.ORCID http://orcid.org/0000-0002-8249-8476
Rudolf UherMRC SGDP Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, England.
Lauren B NavradyDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK.
Mark J AdamsDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK.ORCID http://orcid.org/0000-0002-3599-6018
Yanni ZengDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK.
Archie CampbellCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, Western General Hospital, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0003-0198-5078
Jude GibsonDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK.ORCID http://orcid.org/0000-0002-3745-8360
Pippa A ThomsonCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, Western General Hospital, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-4208-5271
Caroline HaywardMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, Western General Hospital, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-9405-9550
Blair H SmithDivision of Population Health Sciences, University of Dundee, Dundee, UK.ORCID http://orcid.org/0000-0002-5362-9430
Lynne J HockingDivision of Applied Medicine, University of Aberdeen, Aberdeen, UK.
Sandosh PadmanabhanInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
Ian J DearyCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
David J PorteousCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, Western General Hospital, University of Edinburgh, Edinburgh, UK.
Ole MorsPsychosis Research Unit, Aarhus University Hospital, Risskov, Denmark.
Manuel MattheiseniPSYCH, The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Aarhus, Denmark.
Kristin K NicodemusCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, Western General Hospital, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-6165-6471
Andrew M McIntoshDivision of Psychiatry, Royal Edinburgh Hospital, University of Edinburgh, EH10 5HF, Edinburgh, UK. andrew.mcintosh@ed.ac.uk.ORCID http://orcid.org/0000-0002-0198-4588
Royal Edinburgh Hospital · GBWestern General Hospital · GBKing's College London · GBAarhus University · DKAarhus University Hospital · DKDalhousie University · CAUniversity of Aberdeen · GBUniversity of Dundee · GBUniversity of Edinburgh · GBUniversity of Glasgow · GB

Funding

Biotechnology and Biological Sciences Research CouncilChief Scientist Office CZD/16/6Medical Research Council G0700704Medical Research Council MC_PC_17209Medical Research Council MC_UU_00007/10Medical Research Council MR/J000914/1Medical Research Council MR/K026992/1MRF_ C0396Wellcome TrustWellcome Trust 104036/Z/14/Z
6 · The paper itself

Abstract

Antidepressants demonstrate modest response rates in the treatment of major depressive disorder (MDD). Despite previous genome-wide association studies (GWAS) of antidepressant treatment response, the underlying genetic factors are unknown. Using prescription data in a population and family-based cohort (Generation Scotland: Scottish Family Health Study; GS:SFHS), we sought to define a measure of (a) antidepressant treatment resistance and (b) stages of antidepressant resistance by inferring antidepressant switching as non-response to treatment. GWAS were conducted separately for antidepressant treatment resistance in GS:SFHS and the Genome-based Therapeutic Drugs for Depression (GENDEP) study and then meta-analysed (meta-analysis n = 4213, cases = 358). For stages of antidepressant resistance, a GWAS on GS:SFHS only was performed (n = 3452). Additionally, we conducted gene-set enrichment, polygenic risk scoring (PRS) and genetic correlation analysis. We did not identify any significant loci, genes or gene sets associated with antidepressant treatment resistance or stages of resistance. Significant positive genetic correlations of antidepressant treatment resistance and stages of resistance with neuroticism, psychological distress, schizotypy and mood disorder traits were identified. These findings suggest that larger sample sizes are needed to identify the genetic architecture of antidepressant treatment response, and that population-based observational studies may provide a tractable approach to achieving the necessary statistical power.

Indexed as

Data AnalysisHealth ServicesPopulation SurveillanceAdultAntidepressive AgentsCohort StudiesDepressive Disorder, Treatment-ResistantDrug PrescriptionsFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMiddle AgedScotlandAntidepressive Agents

Identifiers

PMID30700811
PMCPMC7096334
OpenAlexW2909754503

What OpenQuestion 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 OpenQuestion graph.