Proportion of Antipsychotics with CYP2D6 Pharmacogenetic (PGx) Associations Prescribed in an Early Intervention in Psychosis (EIP) Cohort: A Cross-Sectional Study

Author:

Jameson Adam123ORCID,Faisal Muhammad345,Fylan Beth235,Bristow Greg C2,Sohal Jaspreet1,Dalton Caroline6,Sagoo Gurdeep S7,Cardno Alastair G8,McLean Samantha L23ORCID

Affiliation:

1. Bradford District Care NHS Foundation Trust, Bradford, UK

2. School of Pharmacy & Medical Sciences, University of Bradford, Bradford, UK

3. Wolfson Centre for Applied Health Research, Bradford, UK

4. Faculty of Health Studies, University of Bradford, Bradford, UK

5. NIHR Yorkshire and Humber Patient Safety Research Collaboration (YH PSRC), Bradford, UK

6. Biomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK

7. Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK

8. Leeds Institute of Health Sciences, Faculty of Medicine and Health, University of Leeds, Leeds, UK

Abstract

Background: Prescribing drugs for psychosis (antipsychotics) is challenging due to high rates of poor treatment outcomes, which are in part explained by an individual’s genetics. Pharmacogenomic (PGx) testing can help clinicians tailor the choice or dose of psychosis drugs to an individual’s genetics, particularly psychosis drugs with known variable response due to CYP2D6 gene variants (‘CYP2D6-PGx antipsychotics’). Aims: This study aims to investigate differences between demographic groups prescribed ‘CYP2D6-PGx antipsychotics’ and estimate the proportion of patients eligible for PGx testing based on current pharmacogenomics guidance. Methods: A cross-sectional study took place extracting data from 243 patients’ medical records to explore psychosis drug prescribing, including drug transitions. Demographic data such as age, sex, ethnicity, and clinical sub-team were collected and summarised. Descriptive statistics explored the proportion of ‘CYP2D6-PGx antipsychotic’ prescribing and the nature of transitions. We used logistic regression analysis to investigate associations between demographic variables and prescription of ‘CYP2D6-PGx antipsychotic’ versus ‘non-CYP2D6-PGx antipsychotic’. Results: Two-thirds (164) of patients had been prescribed a ‘CYP2D6-PGx antipsychotic’ (aripiprazole, risperidone, haloperidol or zuclopenthixol). Over a fifth (23%) of patients would have met the suggested criteria for PGx testing, following two psychosis drug trials. There were no statistically significant differences between age, sex, or ethnicity in the likelihood of being prescribed a ‘CYP2D6-PGx antipsychotic’. Conclusions: This study demonstrated high rates of prescribing ‘CYP2D6-PGx-antipsychotics’ in an EIP cohort, providing a rationale for further exploration of how PGx testing can be implemented in EIP services to personalise the prescribing of drugs for psychosis.

Funder

Bradford District Care NHS Foundation Trust & University of Bradford Scholarship

Publisher

SAGE Publications

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