# Clinically actionable pharmacogenomic landscape of antidepressants and antipsychotics in Qatar: a population-based cohort study

**Authors:** Dinesh Velayutham, Kholoud Bastaki, Areeba Irfan, Mohammed Abuhaliqa, Aisha AlMulla, Suhaila Ghuloum, Muhammad Waqar Azeem, Munir Pirmohamed, Puthen Veettil Jithesh

PMC · DOI: 10.1017/pcm.2025.2 · 2025-04-28

## TL;DR

This study examines how genetic differences in Qataris affect their response to antidepressants and antipsychotics, highlighting the need for personalized treatment approaches.

## Contribution

The study provides population-specific insights into actionable pharmacogenomic variants in Qataris for antidepressants and antipsychotics.

## Key findings

- Actionable metabolizer phenotypes for antidepressants range from 1% to 58% in Qataris.
- For antipsychotics, actionable phenotypes range from 0.1% to 33% based on CYP3A4 and CYP2D6.
- Qataris may require alternative antidepressants, while other populations may only need dosage adjustments.

## Abstract

Consortia like the Clinical Pharmacogenetic Implementation Consortium (CPIC) and the Dutch Pharmacogenetic Working Group (DPWG) provide clinical guidelines but pharmacogenomics implementation depends on population prevalence of actionable genetic variants and response phenotypes. We analyzed the distribution of actionable genetic variants and clinical recommendations in 14,354 adult Qataris, focusing only genes with guidelines (CYP2C19, CYP2D6, CYP2B6 and CYP3A4). Haplotypes and diplotypes were generated from 490 alleles using whole genome data and metabolizer phenotypes were predicted based on current knowledge. Qatari population predicted to have actionable metabolizer phenotypes of CYP2C19, CYP2B6 and CYP2D6 impacting response to antidepressants were in the range of 1%–58% and for antipsychotics 0.1%–33% based on CYP3A4 and CYP2D6. Fine-grained analysis based on clinical guidelines also revealed that while the Qataris may need prescription of an alternate antidepressant not metabolized by CYP2C19, patients from other populations may just need altering the dosage of tricyclic antidepressants like amitriptyline. Further studies incorporating other factors such as diet, environment and cultural habits alongwith population-specific variants will help in the pharmacogenomics implementation in the Qatari population.

## Linked entities

- **Genes:** CYP2C19 (cytochrome P450 family 2 subfamily C member 19) [NCBI Gene 1557], CYP2D6 (cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene)) [NCBI Gene 1565], CYP2B6 (cytochrome P450 family 2 subfamily B member 6) [NCBI Gene 1555], CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576]
- **Chemicals:** amitriptyline (PubChem CID 2160)

## Full-text entities

- **Genes:** CYP2D6 (cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene)) [NCBI Gene 1565] {aka CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2}, CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, CYP2B6 (cytochrome P450 family 2 subfamily B member 6) [NCBI Gene 1555] {aka CPB6, CYP2B, CYP2B7, CYPIIB6, EFVM, IIB1}, CYP2C19 (cytochrome P450 family 2 subfamily C member 19) [NCBI Gene 1557] {aka CPCJ, CYP2C, CYPIIC17, CYPIIC19, P450C2C, P450IIC19}
- **Chemicals:** amitriptyline (MESH:D000639)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12277200/full.md

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Source: https://tomesphere.com/paper/PMC12277200