高血压患者继发依那普利干咳的药物遗传学预测因素。

Q2 Pharmacology, Toxicology and Pharmaceutics
Drug metabolism and personalized therapy Pub Date : 2023-05-19 eCollection Date: 2023-09-01 DOI:10.1515/dmpt-2023-0008
Ivan V Sychev, Natalia P Denisenko, Anastasiya A Kachanova, Anna V Lapshtaeva, Ludmila N Goncharova, Karin B Mirzaev, Dmitry A Sychev
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引用次数: 4

摘要

目的:继发于ACEI咳嗽的发展导致该组药物的停用。通过进一步开发定制的管理方法来评估ACE的安全性是一个重大的科学和实践问题。本研究的目的是评估遗传标志物与原发性动脉高压患者继发于依那普利干咳的药物不良反应发生的关系。方法:对113例依那普利继发性咳嗽患者和104例未发生依那普利副反应的患者进行研究。结果:携带SLCO1B1基因AA rs2306283的患者发生干咳的几率是携带AG和GG基因型患者的2倍(ОR=2.01,95%CI=1.10-3.66,р=0.023),АВО基因rs8176746杂合子患者以干咳形式发生ADR的几率是GG和TT基因型携带者的2.3倍(ОR=2.30,95%CI=1.24-4.29,р=0.008)rs8176746。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacogenetic predictors of development of secondary to enalapril dry cough in hypertensive patients.

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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来源期刊
Drug metabolism and personalized therapy
Drug metabolism and personalized therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.30
自引率
0.00%
发文量
35
期刊介绍: Drug Metabolism and Personalized Therapy (DMPT) is a peer-reviewed journal, and is abstracted/indexed in relevant major Abstracting Services. It provides up-to-date research articles, reviews and opinion papers in the wide field of drug metabolism research, covering established, new and potential drugs, environmentally toxic chemicals, the mechanisms by which drugs may interact with each other and with biological systems, and the pharmacological and toxicological consequences of these interactions and drug metabolism and excretion. Topics: drug metabolizing enzymes, pharmacogenetics and pharmacogenomics, biochemical pharmacology, molecular pathology, clinical pharmacology, pharmacokinetics and drug-drug interactions, immunopharmacology, neuropsychopharmacology.
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