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Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study

Existing algorithms account for ~50% of observed variance in warfarin dose requirements after including common polymorphisms. However, they do not perform as well in populations other than Caucasians, in part because some ethno-specific genetic variants are overlooked. The objective of the present s...

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Autores principales: Claudio-Campos, Karla, Labastida, Aurora, Ramos, Alga, Gaedigk, Andrea, Renta-Torres, Jessicca, Padilla, Dariana, Rivera-Miranda, Giselle, Scott, Stuart A., Ruaño, Gualberto, Cadilla, Carmen L., Duconge-Soler, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461284/
https://www.ncbi.nlm.nih.gov/pubmed/28638342
http://dx.doi.org/10.3389/fphar.2017.00347
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author Claudio-Campos, Karla
Labastida, Aurora
Ramos, Alga
Gaedigk, Andrea
Renta-Torres, Jessicca
Padilla, Dariana
Rivera-Miranda, Giselle
Scott, Stuart A.
Ruaño, Gualberto
Cadilla, Carmen L.
Duconge-Soler, Jorge
author_facet Claudio-Campos, Karla
Labastida, Aurora
Ramos, Alga
Gaedigk, Andrea
Renta-Torres, Jessicca
Padilla, Dariana
Rivera-Miranda, Giselle
Scott, Stuart A.
Ruaño, Gualberto
Cadilla, Carmen L.
Duconge-Soler, Jorge
author_sort Claudio-Campos, Karla
collection PubMed
description Existing algorithms account for ~50% of observed variance in warfarin dose requirements after including common polymorphisms. However, they do not perform as well in populations other than Caucasians, in part because some ethno-specific genetic variants are overlooked. The objective of the present study was to identify genetic polymorphisms that can explain variability in warfarin dose requirements among Caribbean Hispanics of Puerto Rico. Next-Generation Sequencing of candidate genes CYP2C9 and VKORC1 and genotyping by DMET® Plus Assay of cardiovascular patients were performed. We also aimed at characterizing the genomic structure and admixture pattern of this study cohort. Our study used the Extreme Discordant Phenotype approach to perform a case-control association analysis. The CYP2C9 variant rs2860905, which was found in all the major haplotypes occurring in the Puerto Rican population, showed stronger association with warfarin sensitivity (<4 mg/day) than common variants CYP2C9(*)2 and CYP2C9(*)3. Although, CYP2C9(*)2 and CYP2C9(*)3 are separately contained within two of the haplotypes, 10 subjects with the sensitive phenotype were carriers of only the CYP2C9 rs2860905 variant. Other polymorphisms in CES2 and ABCB1 were found to be associated with warfarin resistance. Incorporation of rs2860905 in a regression model (R(2) = 0.63, MSE = 0.37) that also includes additional genetics (i.e., VKORC1-1639 G>A; CYP2C9 rs1856908; ABCB1 c.IVS9-44A>G/ rs10276036; CES2 c.269-965A>G/ rs4783745) and non-genetic factors (i.e., hypertension, diabetes and age) showed better prediction of warfarin dose requirements than CYP2C9(*)2 and CYP2C9(*)3 combined (partial R(2) = 0.132 vs. 0.023 and 0.007, respectively, p < 0.001). The genetic background of Puerto Ricans in the study cohort showed a tri-hybrid admixture pattern, with a slightly higher than expected contribution of Native American ancestry (25%). The genomic diversity of Puerto Ricans is highlighted by the presence of four different major haplotype blocks in the CYP2C9 locus. Although, our findings need further replication, this study contributes to the field by identifying novel genetic variants that increase predictability of stable warfarin dosing among Caribbean Hispanics.
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spelling pubmed-54612842017-06-21 Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study Claudio-Campos, Karla Labastida, Aurora Ramos, Alga Gaedigk, Andrea Renta-Torres, Jessicca Padilla, Dariana Rivera-Miranda, Giselle Scott, Stuart A. Ruaño, Gualberto Cadilla, Carmen L. Duconge-Soler, Jorge Front Pharmacol Pharmacology Existing algorithms account for ~50% of observed variance in warfarin dose requirements after including common polymorphisms. However, they do not perform as well in populations other than Caucasians, in part because some ethno-specific genetic variants are overlooked. The objective of the present study was to identify genetic polymorphisms that can explain variability in warfarin dose requirements among Caribbean Hispanics of Puerto Rico. Next-Generation Sequencing of candidate genes CYP2C9 and VKORC1 and genotyping by DMET® Plus Assay of cardiovascular patients were performed. We also aimed at characterizing the genomic structure and admixture pattern of this study cohort. Our study used the Extreme Discordant Phenotype approach to perform a case-control association analysis. The CYP2C9 variant rs2860905, which was found in all the major haplotypes occurring in the Puerto Rican population, showed stronger association with warfarin sensitivity (<4 mg/day) than common variants CYP2C9(*)2 and CYP2C9(*)3. Although, CYP2C9(*)2 and CYP2C9(*)3 are separately contained within two of the haplotypes, 10 subjects with the sensitive phenotype were carriers of only the CYP2C9 rs2860905 variant. Other polymorphisms in CES2 and ABCB1 were found to be associated with warfarin resistance. Incorporation of rs2860905 in a regression model (R(2) = 0.63, MSE = 0.37) that also includes additional genetics (i.e., VKORC1-1639 G>A; CYP2C9 rs1856908; ABCB1 c.IVS9-44A>G/ rs10276036; CES2 c.269-965A>G/ rs4783745) and non-genetic factors (i.e., hypertension, diabetes and age) showed better prediction of warfarin dose requirements than CYP2C9(*)2 and CYP2C9(*)3 combined (partial R(2) = 0.132 vs. 0.023 and 0.007, respectively, p < 0.001). The genetic background of Puerto Ricans in the study cohort showed a tri-hybrid admixture pattern, with a slightly higher than expected contribution of Native American ancestry (25%). The genomic diversity of Puerto Ricans is highlighted by the presence of four different major haplotype blocks in the CYP2C9 locus. Although, our findings need further replication, this study contributes to the field by identifying novel genetic variants that increase predictability of stable warfarin dosing among Caribbean Hispanics. Frontiers Media S.A. 2017-06-07 /pmc/articles/PMC5461284/ /pubmed/28638342 http://dx.doi.org/10.3389/fphar.2017.00347 Text en Copyright © 2017 Claudio-Campos, Labastida, Ramos, Gaedigk, Renta-Torres, Padilla, Rivera-Miranda, Scott, Ruaño, Cadilla and Duconge-Soler. http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Pharmacology
Claudio-Campos, Karla
Labastida, Aurora
Ramos, Alga
Gaedigk, Andrea
Renta-Torres, Jessicca
Padilla, Dariana
Rivera-Miranda, Giselle
Scott, Stuart A.
Ruaño, Gualberto
Cadilla, Carmen L.
Duconge-Soler, Jorge
Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study
title Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study
title_full Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study
title_fullStr Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study
title_full_unstemmed Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study
title_short Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study
title_sort warfarin anticoagulation therapy in caribbean hispanics of puerto rico: a candidate gene association study
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461284/
https://www.ncbi.nlm.nih.gov/pubmed/28638342
http://dx.doi.org/10.3389/fphar.2017.00347
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