Transporter genes ABCG2 rs2231142 and ABCB1 rs1128503 polymorphisms and atorvastatin response in Chilean subjects
| Primer Autor |
Salazar, Luis A.
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| Co-autores |
Prado, Y.#Zambrano, T.
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| Título |
Transporter genes ABCG2 rs2231142 and ABCB1 rs1128503 polymorphisms and atorvastatin response in Chilean subjects
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| Editorial |
WILEY
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| Revista |
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS
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| Lenguaje |
en
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| Resumen |
What is known and objectiveStatins are first-line therapy for reducing high cholesterol levels. However, response to these drugs shows high interindividual variability. We aimed to investigate the influence of two single nucleotide polymorphisms (SNP) (ABCB1 rs1128503 and ABCG2 rs2231142) in the ABC transporter genes on response to short-term low-dose atorvastatin in Chilean hypercholesterolaemic patients. MethodsWe studied 127 Chilean hypercholesterolaemic patients treated with 10mg/d atorvastatin for 4weeks. The lipid profile was determined before and after drug administration. Genotyping of the rs1128503 and rs2231142 variants was performed using TaqMan((R)) Drug Metabolism Genotyping Assays. Results and discussionGenotype distribution for all polymorphisms investigated was consistent with the Hardy-Weinberg equilibrium. Atorvastatin reduced TC, LDL-C and TG concentrations (P<.05), whereas HDL-C levels were found to be increased (P<.05). Minor allele frequencies for rs1128503 and rs2231142 variants were 0.453 and 0.075, respectively. In this study, patients prescribed with short-term low-dose atorvastatin and carrying ABCB1 (rs1128503) or ABCG2 (rs2231142) SNPs did not show differences in LDL-C response (P>.05). What is new and conclusionThe ABCB1 SNP was not associated with response to atorvastatin in Chilean subjects. The few ABCG2 421A homozygotes did not allow meaningful inferences to be made for this polymorphism.
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| Tipo de Recurso |
Artículo original
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| Description |
This study was supported by grants from Fondecyt, Chile (1130675). Yalena Prado is the current recipient of a fellowship from Conicyt, Chile. Tomas Zambrano is a Postdoctoral Research Fellow at Universidad de La Frontera, Temuco, Chile.
Este estudio fue financiado con fondos de Fondecyt, Chile (1130675). Yalena Prado es actualmente beneficiaria de una beca de Conicyt, Chile. Tomás Zambrano es investigador postdoctoral en la Universidad de La Frontera, Temuco, Chile.
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| doi |
10.1111/jcpt.12607
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| Formato Recurso |
pdf
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| Palabras Claves |
pharmacogenetics# polymorphism# statin
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| Ubicación del archivo |
http://dx.doi.org/10.1111/jcpt.12607
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| Categoría OCDE |
Pharmacology & Pharmacy
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| Materias |
farmacogenética# polimorfismo# estatina
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| Disciplinas de la OCDE |
Farmacología y Farmacia
Genética Humana
Medicina General e Interna
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| Id de Web of Science |
WOS:000419095800013
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| Título de la cita (Recomendado-único) |
Transporter genes <i>ABCG2</i> rs2231142 and <i>ABCB1</i> rs1128503 polymorphisms and atorvastatin response in Chilean subjects
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| Identificador del recurso (Mandatado-único) |
Artículo original
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| Versión del recurso (Recomendado-único) |
version publicada
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| Editorial |
WILEY
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| Revista/Libro |
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS
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| Categoría WOS |
Farmacología y farmacia
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| ISSN |
0269-4727
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| Idioma |
en
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| Referencia del Financiador (Mandatado si es aplicable-repetible) |
ANID FONDECYT 1130675
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| Descripción |
This study was supported by grants from Fondecyt, Chile (1130675). Yalena Prado is the current recipient of a fellowship from Conicyt, Chile. Tomas Zambrano is a Postdoctoral Research Fellow at Universidad de La Frontera, Temuco, Chile.
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| Formato |
pdf
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| Tipo de ruta |
hibrida
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| Access Rights |
metadata
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| Derechos de acceso |
metadata
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| Página de inicio (Recomendado-único) |
255
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| Página final (Recomendado-único) |
272
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