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Self-Reported Medication Use as an Alternate Phenotyping Method for Anxiety and Depression in the UK Biobank

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)389-398
Number of pages10
JournalAmerican Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
Volume186
Issue number6
Early online date18 Oct 2021
DOIs
Accepted/In press7 May 2021
E-pub ahead of print18 Oct 2021

Bibliographical note

Funding Information: This research was conducted using the UK Biobank Resource, under application number 18177. The authors would like to thank all individuals involved in UK Biobank, including the researchers, supporting organizations and of course all the participants who have made a vital contribution to improving health by sharing their experiences. T.C.E. and G.B. were part‐funded during this work by program grants from the UK Medical Research Council (MR/M021475/1 and MR/V012878/1). C.R. is supported by a grant from Fondation Peters to T.C.E. and G.B. G. B. has received honoraria, research or conference grants and consulting fees from Illumina and Otsuka. The authors acknowledge use of the research computing facility at King's College London, Rosalind ( https://rosalind.kcl.ac.uk ), which was part‐funded by capital equipment grants from Guy's and St Thomas' Charity (TR130505) and Maudsley Charity (Award 980). This study represents independent research funded by the National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR, the Department of Health and Social Care or King's College London. Publisher Copyright: © 2021 The Authors. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics published by Wiley Periodicals LLC.

King's Authors

Abstract

The requirement for large sample sizes for psychiatric genetic analyses necessitates novel approaches to derive cases. Anxiety and depression show substantial genetic overlap and share pharmacological treatments. Data on prescribed medication could be effective for inferring case status when other indicators of mental health are unavailable. We investigated self-reported current medication use in UK Biobank participants of European ancestry. Medication Status cases reported using antidepressant or anxiolytic medication (n = 22,218), controls did not report psychotropic medication use (n = 168,959). A subset, “Medication Only,” additionally did not meet criteria for any other mental health indicator (case n = 2,643, control n = 107,029). We assessed genetic overlap between these phenotypes and two published genetic association studies of anxiety and depression, and an internalizing disorder trait derived from symptom-based questionnaires in UK Biobank. Genetic correlations between Medication Status and the three anxiety and depression phenotypes were significant (r g = 0.60–0.73). In the Medication Only subset, the genetic correlation with depression was significant (r g = 0.51). The three polygenic scores explained 0.33% – 0.80% of the variance in Medication Status and 0.07% – 0.19% of the variance in Medication Only. This study provides evidence that self-reported current medication use offers an alternate or supplementary anxiety or depression phenotype in genetic studies where diagnostic information is sparse or unavailable.

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