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Relationship between the CYP2C9 IVS8-109A>T polymorphism and high losartan hydroxylation in healthy Ecuadorian volunteers

  • Pedro Dorado
  • , Alicia Gallego
  • , Eva Peñas-Lledó
  • , Enrique Terán
  • , Adrián Llerena*
  • *Corresponding author for this work
  • University of Extremadura
  • Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM)

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Aim: The CYP2C9 IVS8-109T allele was recently found to be more frequent among Swedish individuals, who have the highest losartan metabolic ratio (MR; losartan:E-3174). Thus, the influence of the CYP2C9 IVS8-109A>T polymorphism on the losartan MR was evaluated among healthy Ecuadorians. In addition, the frequency of the CYP2C9 IVS8-109A>T polymorphism was determined. Results: Among CYP2C9-homozygous wild-types, those with the CYP2C9 IVS8-109T/T versus A/A genotypes had a lower MR (p < 0.05). Furthermore, the frequency of the CYP2C9 IVS8-109T variant was lower in Ecuadorians (21.4%; p < 0.001) than in populations from Sweden or Asia (ranging from 32 to 46%). Conclusion: In this Ecuadorian population, the CYP2C9 IVS8-109T allele was associated with an increased CYP2C9 hydroxylation capacity. Further investigation needs to be carried out in order to clarify the relevance of the SNP of CYP2C9 IVS8-109A>T on losartan hydroxylation across populations and its potential implications in CYP2C9 activity. Original submitted 19 February 2014; Revision submitted 16 May 201.

Original languageEnglish
Pages (from-to)1417-1421
Number of pages5
JournalPharmacogenomics
Volume15
Issue number11
DOIs
StatePublished - 1 Aug 2014

Keywords

  • CYP2C9
  • IVS8-109A>T
  • intronic polymorphism
  • losartan

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