# Addressing genetic diversity and health inequities: RELIVAF’s proposal for Latin American pharmacogenomic guidelines

**Authors:** Luis A. Quiñones, Matías F. Martínez, Rodrigo Vargas, Leslie C. Cerpa, Andrés López-Cortés, Farith González-Martínez, Dora Fonseca, Jorge Duconge, Nelson M. Varela, Ismael Lares-Asseff, María Ana Redal, Patricia Esperón, Fabricio Ríos-Santos, Ana Lucía Rendón, Roberto Serrano, Elizabeth Ortega, Luis Sullón-Dextre, Enrique Sanchez, María Laura Arias, Diadelis Remírez, Alexis Morales

PMC · DOI: 10.3389/fphar.2026.1721828 · 2026-01-22

## TL;DR

This paper introduces RELIVAF, a framework to develop Latin American pharmacogenomic guidelines that consider the region's genetic diversity and healthcare needs.

## Contribution

RELIVAF proposes a novel framework for region-specific pharmacogenomic guidelines tailored to Latin America's admixed populations.

## Key findings

- Current pharmacogenomic guidelines are not well-suited for Latin America's admixed populations.
- RELIVAF integrates allele frequencies, drug availability, and implementation constraints to create region-specific guidelines.
- Three gene-drug pairs were prioritized for initial guidelines due to their clinical relevance and public health impact.

## Abstract

Latin America’s exceptional genetic diversity, shaped by centuries of admixture among Native American, European, and African ancestries, presents both challenges and opportunities for pharmacogenomic implementation. Current guidelines by CPIC and DPWG, though foundational, are largely based on European and East Asian data, limiting their applicability in highly admixed populations. This article presents the rationale and methodology of RELIVAF (Latin American Network for the Implementation and Validation of Pharmacogenomic Clinical Guidelines), which aims to produce region-specific recommendations aligned with local genetic profiles, healthcare systems, and regulatory landscapes. The framework integrates international standards with country- and ancestry-specific allele frequencies, effect sizes, drug availability, and implementation constraints. It also incorporates educational strategies to promote pharmacogenomic literacy among healthcare professionals. Three gene-drug pairs were prioritized for initial guideline development: DPYD-fluoropyrimidines, TPMT/NUDT15–thiopurines (paediatric ALL), and CYP2C9/VKORC1-coumarin anticoagulants (e.g., warfarin, acenocoumarol). Selection was based on clinical relevance, allele frequency variability, and potential public health impact. By leveraging regional data and collaborative expertise, RELIVAF aims to deliver actionable, equitable, and context-specific pharmacogenomic guidance, advancing precision medicine in Latin America and serving as a model for other underrepresented regions.

## Linked entities

- **Genes:** DPYD (dihydropyrimidine dehydrogenase) [NCBI Gene 1806], TPMT (thiopurine S-methyltransferase) [NCBI Gene 7172], NUDT15 (nudix hydrolase 15) [NCBI Gene 55270], CYP2C9 (cytochrome P450 family 2 subfamily C member 9) [NCBI Gene 1559], VKORC1 (vitamin K epoxide reductase complex subunit 1) [NCBI Gene 79001]
- **Chemicals:** warfarin (PubChem CID 54678486), acenocoumarol (PubChem CID 54676537)
- **Diseases:** paediatric ALL (MONDO:0000870)

## Full-text entities

- **Genes:** VKORC1 (vitamin K epoxide reductase complex subunit 1) [NCBI Gene 79001] {aka EDTP308, MST134, MST576, VKCFD2, VKOR}, NUDT15 (nudix hydrolase 15) [NCBI Gene 55270] {aka MTH2, NUDT15D}, TPMT (thiopurine S-methyltransferase) [NCBI Gene 7172] {aka TPMTD}, CYP2C9 (cytochrome P450 family 2 subfamily C member 9) [NCBI Gene 1559] {aka CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9}
- **Chemicals:** acenocoumarol (MESH:D000074), coumarin (MESH:C030123), DPYD (MESH:C036020), thiopurines (MESH:C520399), fluoropyrimidines (-), warfarin (MESH:D014859)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12872856/full.md

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Source: https://tomesphere.com/paper/PMC12872856