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Local ancestry-informed candidate pathway analysis of warfarin stable dose in latino populations.

Heidi E SteinerKelvin Carrasquillo CarrionJason B GilesAbiel Roche-LimaKevin YeeXiaoxiao SunLarisa H CavallariMinoli A PereraJorge DucongeJason H Karnes
Published in: Clinical pharmacology and therapeutics (2022)
Accuracy of warfarin dose prediction algorithms may be improved by including data from diverse populations in genetic studies of dose variability. Here, we surveyed single nucleotide polymorphisms in vitamin K-related genes for association with warfarin dose requirements in two admixed Latino populations in standard-principal component adjusted and contemporary-local ancestry adjusted regression models. A total of 5 variants from vitamin K-related genes/pathways were associated with warfarin dose in both cohorts (p<0.0125) in standard models. Local ancestry-adjusted analysis unveiled 35 associated variants with absolute effects ranging from β = 9.04 (±2.23) to 39.18 (±10.89) per ancestral allele in the discovery cohort and β = 6.47 (±2.02) to 17.82 (±6.83) in the replication cohort. Importantly, we demonstrate the technical validity of the Tractor model in cohorts with admixed ancestry from three founder populations and bring attention to the technical hurdles obstructing the inclusion of diverse, especially admixed, populations in pharmacogenomic research.
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