DOI

  • Michael S. Zastrozhin
  • Valentin Y. Skryabin
  • Marco Torrado
  • Anastasiya Petrovna
  • Alexander S. Sorokin
  • Elena A. Grishina
  • Kristina A. Ryzhikova
  • Inessa A. Bedina
  • Oleg Z. Buzik
  • Egor M. Chumakov
  • Ludmila M. Savchenko
  • Evgeny A. Brun
  • Dmitry A. Sychev

Introduction: Phenazepam therapy can often be ineffective and some patients develop dose-related adverse drug reactions. Aim. The purpose of this research was to study the effect of the CYP2C19*2 (681G>A, rs4244285) in patients with anxiety disorders and alcohol dependence taking phenazepam therapy. Materials & methods: Patients (175 males, average age: 37.16 ± 7.84 years) received phenazepam in tablet form for 5 days. Genotyping was performed by real-Time polymerase chain reaction. Results: The statistically significant differences in the UKU Side-Effect Rating Scale scores on the fifth day of therapy: (CYP2C19*1/*1) 2.00 [1.00; 2.00), (CYP2C19*1/*2) 7.00 (7.00; 7.00), (CYP2C19*2/*2) 9.00 (8.00; 9.00), p < 0.001. Conclusion: This study demonstrated the different efficacy and safety of phenazepam in patients with different genotypes of CYP2C19*2.

Original languageEnglish
Pages (from-to)111-123
Number of pages13
JournalPharmacogenomics
Volume21
Issue number2
Early online date20 Jan 2020
DOIs
StatePublished - Jan 2020

    Research areas

  • alcohol addiction, anxiety disorders, benzodiazepines, biotransformation, bromodihydrochlorobenzodiazepine, personalized medicine, phenazepam, Anxiety Disorders/drug therapy, Anti-Anxiety Agents/administration & dosage, Humans, Genotype, Male, Benzodiazepines/administration & dosage, Adult, Cytochrome P-450 CYP2C19/genetics, Female, Alcoholism/genetics, SUBSTANCE-ABUSE, CYP2C19, MOOD, CYP2D6, MIDAZOLAM, DEPRESSION, GENETIC POLYMORPHISMS, HALOPERIDOL, BENZODIAZEPINES, RESPONSES, bromodihydrochloroben-zodiazepine

    Scopus subject areas

  • Genetics
  • Molecular Medicine
  • Pharmacology

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