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

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.
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…
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Taxonomy
TopicsPharmacogenetics and Drug Metabolism · Genomics and Rare Diseases · BRCA gene mutations in cancer
