Genetic and clinical characteristics of treatment-resistant depression using primary care records in two UK cohorts.


Journal

Molecular psychiatry
ISSN: 1476-5578
Titre abrégé: Mol Psychiatry
Pays: England
ID NLM: 9607835

Informations de publication

Date de publication:
07 2021
Historique:
received: 26 10 2020
accepted: 24 02 2021
revised: 12 02 2021
pubmed: 24 3 2021
medline: 27 1 2022
entrez: 23 3 2021
Statut: ppublish

Résumé

Treatment-resistant depression (TRD) is a major contributor to the disability caused by major depressive disorder (MDD). Primary care electronic health records provide an easily accessible approach to investigate TRD clinical and genetic characteristics. MDD defined from primary care records in UK Biobank (UKB) and EXCEED studies was compared with other measures of depression and tested for association with MDD polygenic risk score (PRS). Using prescribing records, TRD was defined from at least two switches between antidepressant drugs, each prescribed for at least 6 weeks. Clinical-demographic characteristics, SNP-based heritability (h

Identifiants

pubmed: 33753889
doi: 10.1038/s41380-021-01062-9
pii: 10.1038/s41380-021-01062-9
pmc: PMC8505242
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3363-3373

Subventions

Organisme : Medical Research Council
ID : MR/P00167X/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N015746
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S015132/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_QA137853
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_17228
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S0151132
Pays : United Kingdom

Informations de copyright

© 2021. The Author(s).

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Auteurs

Chiara Fabbri (C)

Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.

Saskia P Hagenaars (SP)

Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

Catherine John (C)

Department of Health Sciences, University of Leicester, Leicester, UK.

Alexander T Williams (AT)

Department of Health Sciences, University of Leicester, Leicester, UK.

Nick Shrine (N)

Department of Health Sciences, University of Leicester, Leicester, UK.

Louise Moles (L)

Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

Ken B Hanscombe (KB)

Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

Alessandro Serretti (A)

Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.

David J Shepherd (DJ)

Department of Health Sciences, University of Leicester, Leicester, UK.

Robert C Free (RC)

NIHR Leicester Biomedical Research Centre, University of Leicester, Leicester, UK.
Department of Respiratory Sciences, University of Leicester, Leicester, UK.

Louise V Wain (LV)

Department of Health Sciences, University of Leicester, Leicester, UK.
NIHR Leicester Biomedical Research Centre, University of Leicester, Leicester, UK.

Martin D Tobin (MD)

Department of Health Sciences, University of Leicester, Leicester, UK.
NIHR Leicester Biomedical Research Centre, University of Leicester, Leicester, UK.

Cathryn M Lewis (CM)

Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK. cathryn.lewis@kcl.ac.uk.
Department of Medical and Molecular Genetics, Faculty of Life Sciences and Medicine, King's College London, London, UK. cathryn.lewis@kcl.ac.uk.

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