Evidence map›Paper›PMID 35602235›Full record

ArticleCommunications medicine2021

Understanding genetic risk factors for common side effects of antidepressant medications.

Adrian I Campos, Aoibhe Mulcahy, Jackson G Thorp, Naomi R Wray, Enda M Byrne, Penelope A Lind, Sarah E Medland, Nicholas G Martin, Ian B Hickie, Miguel E Rentería

Open access · goldAbstract read
In one paragraph

Article in Communications medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

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  6. Understanding antidepressant change patterns in the UK Biobank.The British journal of psychiatry : the journal of mental science · 2026
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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

10 authors at 4 institutions in 1 country.

Adrian I CamposDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD Australia.ORCID 0000-0003-3468-8619
Aoibhe MulcahyDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD Australia.
Jackson G ThorpDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD Australia.
Naomi R WrayInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD Australia.ORCID 0000-0001-7421-3357
Enda M ByrneInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD Australia.
Penelope A LindDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD Australia.
Sarah E MedlandDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD Australia.ORCID 0000-0003-1382-380X
Nicholas G MartinDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD Australia.ORCID 0000-0003-4069-8020
Ian B HickieBrain and Mind Centre, University of Sydney, Camperdown, NSW Australia.
Miguel E RenteríaDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD Australia.ORCID 0000-0003-4626-7248
The University of Queensland · AUQIMR Berghofer Medical Research Institute · AUQueensland University of Technology · AUThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Major depression is one of the most disabling health conditions internationally. In recent years, new generation antidepressant medicines have become very widely prescribed. While these medicines are efficacious, side effects are common and frequently result in discontinuation of treatment. Compared with specific pharmacological properties of the different medications, the relevance of individual vulnerability is understudied. Methods: We used data from the Australian Genetics of Depression Study to gain insights into the aetiology and genetic risk factors to antidepressant side effects. To this end, we employed structural equation modelling, polygenic risk scoring and regressions. Results: Here we show that participants reporting a specific side effect for one antidepressant are more likely to report the same side effect for other antidepressants, suggesting the presence of shared individual or pharmacological factors. Polygenic risk scores (PRS) for depression associated with side effects that overlapped with depressive symptoms, including suicidality and anxiety. Body Mass Index PRS are strongly associated with weight gain from all medications. PRS for headaches are associated with headaches from sertraline. Insomnia PRS show some evidence of predicting insomnia from amitriptyline and escitalopram. Conclusions: Our results suggest a set of common factors underlying the risk for antidepressant side effects. These factors seem to be partly explained by genetic liability related to depression severity and the nature of the side effect. Future studies on the genetic aetiology of side effects will enable insights into their underlying mechanisms and the possibility of risk stratification and prophylaxis strategies.

Indexed as

EpidemiologyPharmacogenomics

Identifiers

PMID35602235
PMCPMC9053224
OpenAlexW3213756041

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.