Pharmacogenetic predictors of development of secondary to enalapril dry cough in hypertensive patients
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Ivan V. Sychev
, Natalia P. Denisenko
, Anastasiya A. Kachanova
, Anna V. Lapshtaeva
, Ludmila N. Goncharova
, Karin B. Mirzaev
and Dmitry A. Sychev
Abstract
Objectives
Development of the secondary to ACEI cough leads to discontinuation of the drugs of this group. Assessing the safety of the ACEIs with further development of customized approaches for their administration is a major scientific and practical problem. The objective of this study was to assess the association of the genetic markers with the development of the adverse drug reaction in the form of secondary to enalapril dry cough in the patients with essential arterial hypertension.
Methods
Study involved 113 patients with the secondary to enalapril cough and 104 patients without development of the secondary to enalapril adverse drug reaction.
Results
The patients carriers of the genotype AA rs2306283 of gene SLCO1B1 had 2-fold higher odds of developing the dry cough than those with the genotypes AG and GG (ОR=2.01, 95%CI=1.10–3.66, р=0.023). Similarly, the patients heterozygous for rs8176746 of gene АВО had 2.3-fold higher odds of developing the ADR in the form of dry cough than the carriers of the genotypes GG and TT (ОR=2.30, 95%CI=1.24–4.29, р=0.008).
Conclusions
Statistically significant association between the development of the ADR in the form of secondary to enalapril dry cough and polymorphisms rs2306283 of gene SLCO1B1 and rs8176746 of gene ABO was revealed.
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Research funding: The work was performed as part of the Russian Federation Ministry of Health state assignment for the years 2021–2023, no. 121110800062-6 “New Pharmacogenetic Biomarkers of Safety of Pharmacotherapy for Certain Socially Significant Diseases”. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Informed consent: Informed consent was obtained from all individuals included in this study.
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Ethical approval: The study complied with the requirements of the World Medical Association’s Declaration of Helsinki and was approved by the Local Ethics Committee of the Ogarev Mordovia State University (Protocol No. 91 of 12/23/2020).
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Articles in the same Issue
- Frontmatter
- Editorial
- Relevance of personalized medicine for improving traditional medicine
- Review
- Mechanistic role and potential of Ayurvedic herbs as anti-aging therapies
- Original Articles
- Safety, immunogenecity and effectiveness of ChAdOx1 nCoV-19 vaccine during the second wave of pandemic in India: a real-world study
- Evaluation of the efficacy of topical Terminalia chebula Retz. with vinegar in the treatment of tinea corporis: a non-inferiority randomized controlled trial
- Pharmacogenetic predictors of development of secondary to enalapril dry cough in hypertensive patients
- Genetic markers associated with adverse reactions of radioiodine therapy in thyroid cancer patients
- Lack of exposure to pharmacogenomics education among the health care providing students in the West Bank of Palestine
- Development and validation wise assessment of genotype guided warfarin dosing algorithm in Indian population
- Exploratory quasi-experimental study of anti-arthritic activity of Ayurvedic polyherbal formulation, Abha Guggulu in osteoarthritis patients
- Letter to the Editor
- Ayurvedic medicines in alleviating the symptoms of SARS-CoV-2 omicron variant in North Indian population: a regional genomic study