BRIEF RESEARCH REPORT article

Front. Genet.

Sec. Pharmacogenetics and Pharmacogenomics

Allelic diversity of the pharmacogenes CYP2D6 and CYP2C19 in Māori from Te Tairāwhiti, Aotearoa New Zealand

  • 1. Department of Pathology and Biomedical Science, University of Otago Christchurch, Christchurch, New Zealand

  • 2. Department of Womens and Childrens Health, University of Otago, Dunedin, New Zealand

  • 3. Ngati Porou Oranga, Gisborne, New Zealand

  • 4. Department of Mathematics and Statistics, University of Otago, Dunedin, New Zealand

The final, formatted version of the article will be published soon.

Abstract

CYP2C19 and CYP2D6 are two important pharmacogenes responsible for metabolising a wide range of medications. Both genes exhibit a high level of variation, which can lead to variable activity of the enzymes they encode, with risks of adverse drug reactions and treatment failure. Understanding this variation is therefore of great importance, but the full extent of variability in these genes is not yet documented, particularly for understudied populations. We employed targeted nanopore sequencing to identify genetic variants within CYP2C19 and CYP2D6 for a group of Māori individuals, largely affiliated with the Ngāti Porou iwi from Te Tairāwhiti (Gisborne), Aotearoa New Zealand. 135 CYP2D6 and 73 CYP2C19 genotypes were sequenced, with metaboliser phenotypes inferred for the majority of participants. CYP2D6 normal metabolisers make up 54% of the cohort and 45% of the cohort are CYP2C19 intermediate metabolisers. Nearly 20% had an uncertain CYP2D6 activity due to the prevalence of CYP2D6*71, which is of unknown functional impact. Understanding the extent of variation in these genes should contribute to equitable application of pharmacogenetic testing in Aotearoa New Zealand.

Summary

Keywords

ancestry, CYP2C19, CYP2D6, diversity, drug metabolism (human and animal), drug response, Indigeneous, nanopore sequencing

Received

17 July 2025

Accepted

19 February 2026

Copyright

© 2026 Hitchman, Kerekere, Miller, Goodin, Koia, Watson, King, Robertson, Wilcox and Kennedy. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Martin A Kennedy

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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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