Abstract

Introduction: Phenazepam is the Russian original benzodiazepine tranquilizer. We conducted first pharmacogenetic study on Phenazepam’s safety in patients with alcohol withdrawal syndrome. Isoenzymes CYP3A4, CYP3A5, CYP2C9, and CYP2C19 are involved into benzodiazepine tranquilizers’ metabolism.Aim: To determine predictive value of CYP3A5, CYP2C9, CYP2C19, and CYP2D6 genetic polymorphisms and their haplotypes for adverse reaction risk associated with the treatment with phenazepam.Materials and methods: The study enrolled 102 male patients with non-comlicated alcohol withdrawal syndrome (F10.3 by ICD-10) who entered the study group in 24 hours after the admission to hospital and was administered Phenazepam for 6 days. Therapy safety was evaluated with UKU Side Effects Rating Scale on the 6th day of treatment. 5 ml of venous blood was collected from each participant for genotyping to detect CYP3A5*3, CYP2С9*2, CYP2C9*3, CYP2C19*2, CYP2C19*3, CYP2C19*17, and CYP2D6*4 polymorphisms by real-time polymerase chain reaction. Haplotype analysis was performed by SNPStats online-tool. Statistical analysis was made in SPSS Statistics 21.0.Results: In overall sample (n=102) CYP2C9*3 increased risk of «Increased duration of sleep» (OR 1.46; 95% CI 1.11−1.9; p=0.037) and «Constipation» (OR 13.1; 95% CI 1.44−119.2; p=0.02). The following results in subgroup «Phenazepam’s monotherapy» (n=64) were observed: CYP3A5*3 increased global severity of adverse drug reactions according to patient’s opinion (OR 2.79; 95% CI 1.26−6.22; p=0.031); CYP2C9*3 led to «Increased duration of sleep» (OR 1.57; 95% CI 1.14−2.17; p=0.034). Haplotype CYP3A5*3-CYP2C19*2-CYP2C19*17 (G-G-T) was associated with increased risk of «Concentration difficulties (OR 2.86; 95% CI 0.96−8.50; p=0.061).Conclusion: The study findings confirmed that CYP2C9*3, CYP3A5*3, and CYP2C19*2 polymorphisms can decrease the phenazepam safety rate in patients with alcohol withdrawal syndrome. The result of haplotype analysis revealed that only CYP3A5*3-CYP2C19*2-CYP2C19*17 (G-G-T) can be used as a significant predictor of adverse reaction to phenazepam.

Highlights

  • Phenazepam is the Russian original benzodiazepine tranquilizer

  • Цель исследования ― проанализировать влияние полиморфизмов генов CYP3A5, CYP2C9, CYP2C19 и CYP2D6 на профиль безопасности феназепама при синдроме отмены алкоголя с расчетом чувствительности и специфичности каждого биомаркера, а также с проведением гаплотипического анализа

  • Aim: To determine predictive value of CYP3A5, CYP2C9, CYP2C19, and CYP2D6 genetic polymorphisms and their haplotypes for adverse reaction risk associated with the treatment with phenazepam

Read more

Summary

НАУЧНОЕ ИССЛЕДОВАНИЕ ORIGINAL STUDY

Вестник РАМН. — 2018. — Т.73. — No3. — С. 206–214. Annals of the Russian academy of medical sciences. 2018;73(3):206214. Цель ― проанализировать влияние полиморфизмов генов CYP3A5, CYP2C9, CYP2C19 и CYP2D6 на профиль безопасности феназепама при синдроме отмены алкоголя. (Для цитирования: Иващенко Д.В., Рыжикова К.А., Созаева Ж.А., Пименова Ю.А., Гришина Е.А., Застрожин М.С., Агузаров А.Д., Савченко Л.М., Брюн Е.А., Сычёв Д.А. Влияние полиморфизмов генов CYP3A5, CYP2C9, CYP2C19 и CYP2D6 на профиль безопасности феназепама при синдроме отмены алкоголя. Результаты ассоциативных фармакогенетических исследований полиморфизмов генов CYP3A5*3, CYP2C9*2 и *3, CYP2C19*2 и *17, CYP2D6*4, посвященных вопросам безопасности применения феназепама у пациентов с синдромом отмены алкоголя, были опубликованы нами ранее [17−20]. Цель исследования ― проанализировать влияние полиморфизмов генов CYP3A5, CYP2C9, CYP2C19 и CYP2D6 на профиль безопасности феназепама при синдроме отмены алкоголя с расчетом чувствительности и специфичности каждого биомаркера, а также с проведением гаплотипического анализа. Impact of CYP3A5, CYP2C9, CYP2C19, and CYP2D6 Polymorphisms on Phenazepam Safety in Patients with Alcohol

Introduction
Генотипы и аллели n
Большая выраженность НПР по мнению пациента
Увеличение яркости и интенсивности сновидений
Findings
Участие авторов
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call