# Effect of CYP1A2, CYP2D6, and CYP3A4 Variation on Antipsychotic Treatment Outcomes

**Authors:** Lauren Varney, Stephen Murtough, Marius Cotic, Rosemary Abidoph, Lian Chan, Noushin Saadullah Khani, Alvin Richards-Belle, Maria Richards-Brown, Daisy Mills, Daniele Panconesi, Yogita Dawda, Parveen Sharma, Chetan Shah, Agostina Secchi, Ramin Nilforooshan, Santosh Mudholkar, Rosie Murdoch, Jazmin Molai, Rebecca Griffiths, Suruthy Senthilkumar, Helen Blake, Steve Lankshear, Jennifer McRoberts, Bethany Pastor, Carmel Thomas, Sabrina Richards, Alison Welfare-Wilson, Sai-Bo Cheung, Rebecca Cox, Anita Chinazam Jibero, Reanne Anad, Rebeka Laczik, Sharif Ghali, Alex J. Berry, Joanna Curwen, Koye Odutoye, Girija Kottalgi, Sally Williams, Solomon Wong, Nithya Anandan, Georgy Pius, Tonye Ajiteru, Victoria Clark, Philip van Driel, Amir Bashir, Samantha Court, Minerva Pawsey, Anna Skowronska, Jessica Woodley, Elvira Bramon

PMC · DOI: 10.3390/ph18060892 · Pharmaceuticals · 2025-06-14

## TL;DR

This study shows that genetic variations in CYP enzymes can affect how well people respond to antipsychotic medications and their side effects.

## Contribution

The study demonstrates a link between CYP gene variants and antipsychotic treatment outcomes, including adverse reactions and quality of life.

## Key findings

- Ultrarapid CYP2D6 metabolizers reported fewer adverse drug reactions.
- CYP1A2*30 carriers showed suggestive evidence of lower quality of life scores.
- Over half of participants had alleles linked to altered antipsychotic metabolism.

## Abstract

Background/Objectives: Antipsychotic treatment response varies considerably between individuals, with one potential reason being genetic variation affecting the cytochrome P450 enzymes that metabolise them. Methods: With a diverse sample of 453 participants, we studied the influence of CYP1A2, CYP2D6, and CYP3A4 variation on three antipsychotic treatment outcomes: participant-reported adverse antipsychotic drug reactions, health-related quality of life, and the dose of antipsychotic medication prescribed. These measures were taken from the baseline assessment, before a pharmacogenetic intervention was delivered. Results: Over half of our sample (62.9%) were carriers of an allele associated with altered metabolism of antipsychotic medications on CYP2D6 or CYP3A4, the two genes with pharmacogenetic guidelines for antipsychotic medications. Ultrarapid CYP2D6 metabolisers reported significantly lower levels of adverse antipsychotic drug reactions than normal CYP2D6 metabolisers (mean difference: −11.1; 95% confidence interval [CI]: −18.9, −3.3; p = 0.00575). There was also suggestive evidence of lower quality of life scores in those carrying one (mean difference: −0.0863; 95% CI: −0.1806, 0.0081; p = 0.0731) or two copies (mean difference: −0.0803; 95% CI: −0.1734, 0.0129; p = 0.0914) of the CYP1A2*30-inducible allele. Conclusions: Our findings suggest that even when looking at a small number of cytochrome P450 genes, carrying an allele associated with altered antipsychotic medication metabolism is relatively common. We also found evidence that the CYP genotype can influence antipsychotic treatment outcomes, specifically adverse drug reactions and quality of life scores.

## Linked entities

- **Genes:** CYP1A2 (cytochrome P450 family 1 subfamily A member 2) [NCBI Gene 1544], CYP2D6 (cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene)) [NCBI Gene 1565], CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576]

## Full-text entities

- **Genes:** CYP1A2 (cytochrome P450 family 1 subfamily A member 2) [NCBI Gene 1544] {aka CP12, CYPIA2, P3-450, P450(PA)}, CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, CYP2D6 (cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene)) [NCBI Gene 1565] {aka CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2}

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12196257/full.md

## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC12196257/full.md

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Source: https://tomesphere.com/paper/PMC12196257