Literature DB >> 31932355

Association between polymorphisms in microRNA seed region and warfarin stable dose.

Maryam Hosseindokht1, Hamed Zare2, Rasoul Salehi1, Leyla Pourgholi3, Shayan Ziaee3, Mohammadali Boroumand4, Mohammadreza Sharifi5.   

Abstract

BACKGROUND: The optimal dose of anticoagulant warfarin varies among patients to achieve the target international normalised ratio. Although genetic variations related to warfarin pharmacokinetics and vitamin K cycle are important factors associated with warfarin dose requirements, these variations do not completely explain the large interindividual variability observed in the most populations, suggesting that additional factors may contribute to this variability. microRNAs have recently been introduced as regulators of drug function genes, and therefore, may be involved in drug responses. In this study, we aimed to evaluate the possible association between variants in the seed region of microRNAs, which target the genes involved in the action of warfarin and warfarin dose requirement.
METHODS: 526 samples were collected from Iranian patients. Four selected polymorphisms in the seed region of microRNAs (rs2910164, rs66683138, rs12416605 and rs35770269 in miR-146a, miR-3622a, miR-938 and miR-449c, respectively) were genotyped by PCR-restriction fragment length polymorphism method.
RESULTS: rs2910164 C/G in the seed region of miR-146a was associated with warfarin dose requirement (p<0.001); the patients with GG genotype had the higher mean dose of warfarin (40.6 mg/week, compared with 33.9 and 31.8 mg/week for GC and CC genotypes, respectively). The association of other polymorphisms with warfarin dose requirement was not statistically significant.
CONCLUSION: rs2910164 C/G in the seed region of miR-146a is associated with warfarin maintenance dose, likely by disrupting interaction between miR-146a and ATP-binding cassette subfamily B member 1 gene, ABCB1. Therefore, this polymorphism may possibly be a potential factor for assessment of warfarin dose requirements. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  clinical pharmacology

Year:  2020        PMID: 31932355     DOI: 10.1136/postgradmedj-2019-137197

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


  1 in total

1.  Plasma miRNA profiles associated with stable warfarin dosage in Chinese patients.

Authors:  Li Zhao; Jin Wang; Shaoxin Shi; Yuan Wu; Jumei Liu; Shiwei He; Yue Zou; Huabin Xie; Shengxiang Ge; Huiming Ye
Journal:  PeerJ       Date:  2020-10-13       Impact factor: 2.984

  1 in total

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