Evidence map›Paper›PMID 41142254›Full record

ArticleFrontiers in pharmacology2025

Patient and clinician perspectives on pharmacogenetic testing for antipsychotics.

Maria Richards-Brown, Yiran Wei, Rosemary Abidoph, Lauren Varney, Marius Cotic, Stephen Murtough, Daniele Panconesi, Daisy Mills, Alvin Richards-Belle, Noushin Saadullah Khani and 3 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

13 authors.

Maria Richards-BrownDivision of Psychiatry, University College London, London, United Kingdom.
Yiran WeiDivision of Psychiatry, University College London, London, United Kingdom.
Rosemary AbidophDivision of Psychiatry, University College London, London, United Kingdom.
Lauren VarneyDivision of Psychiatry, University College London, London, United Kingdom.
Marius CoticDivision of Psychiatry, University College London, London, United Kingdom.
Stephen MurtoughDivision of Psychiatry, University College London, London, United Kingdom.
Daniele PanconesiDivision of Psychiatry, University College London, London, United Kingdom.
Daisy MillsDivision of Psychiatry, University College London, London, United Kingdom.
Alvin Richards-BelleDivision of Psychiatry, University College London, London, United Kingdom.
Noushin Saadullah KhaniDivision of Psychiatry, University College London, London, United Kingdom.
Beverley ChippSideBySide Network, St Pancras Hospital, London, United Kingdom.
Elvira BramonDivision of Psychiatry, University College London, London, United Kingdom.
Nicola MorantDivision of Psychiatry, University College London, London, United Kingdom.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background/objectives: Medications to treat psychosis (i.e., antipsychotics) have common and sometimes serious adverse drug reactions and can require several trials before finding a suitable drug and dose. To address this, there is increasing focus on personalizing medicine. Pharmacogenetics investigates how genetic variation influences drug metabolism and response, with recent clinical trials suggesting pharmacogenetic testing can improve remission and reduce adverse drug reactions. Therefore, understanding stakeholder perspectives on acceptability is critical. Methods: This pilot study is part of 'GEMS' (Genetics and Environment in Mental Health Study), which investigates pharmacogenetic testing for psychosis. A participant survey, co-created with patients, was completed by 22 patient-participants, and semi-structured interviews were conducted with 11 clinician-participants who had used pharmacogenetic test reports with patients. Results: Both patients and clinicians were generally positive about pharmacogenetics, although clinicians saw this as just one component in the multifactorial process of individualized prescribing. Clinicians and patients both suggested a more user-friendly format of the pharmacogenetic report to enhance patient understanding. Some described the reports as promoting more collaborative care, but this was not universal. Clinicians highlighted both retrospective and prospective value in pharmacogenetics providing more certainty through reducing 'trial-and-error' prescribing. However, accessibility, understanding, and logistics were identified as potential barriers to implementation. Conclusion: Among patients and clinicians who have experienced pharmacogenetic testing to inform antipsychotic prescribing, acceptability is good. There is potential for pharmacogenetics to enhance personalized prescribing, but barriers to widespread implementation remain.

Indexed as

antipsychoticsmental healthpersonalized medicinepharmacogeneticspsychiatrypsychosis

Identifiers

PMID41142254
PMCPMC12547232

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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.