UGT1A4和ABCB1多态性对土耳其精神分裂症患者氯氮平和N-去甲基氯氮平血浆水平的影响

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Fezile Ozdemir, Merve Demirbugen Oz, Kenan Can Tok, Emrah Dural, Yagmur Kır, Mehmet Gumustas, Bora Baskak, H Sinan Suzen
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引用次数: 0

摘要

氯氮平(CLZ)是一种抗精神病药物,特别用于对其他药物无反应的治疗抵抗性精神分裂症患者。这是首选,因为它减少自杀行为和企图,减少侵略和暴力行为。本研究旨在评估ABCB1 rs1045642和UGT1A4 rs2011425多态性对精神分裂症患者CLZ及其主要代谢物N-地甲基氯氮平(DCLZ)血药浓度的影响。共纳入109名持续给予CLZ单药治疗的土耳其精神分裂症患者。液液萃取后,采用高效液相色谱法检测血浆中CLZ和DCLZ的浓度,采用PCR- RFLP法检测转运体基因ABCB1和二相酶UGT1A4的多态性。结果显示,UGT1A4*3多态性对亚治疗水平/上治疗水平患者的CLZ C/D和DCLZ C/D水平有统计学意义,而ABCB1 C3435T多态性对亚治疗水平患者的CLZ/DCLZ比值有统计学意义。本研究提示了遗传差异对血浆水平的影响,强调了药物遗传学研究在临床中的重要性。使用获得的结果作为药物遗传生物标志物将帮助临床医生为个别患者提供有效的治疗,并减少不良的副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effects of UGT1A4 and ABCB1 polymorphisms on clozapine and N- desmethyl clozapine plasma levels in Turkish schizophrenia patients.

Clozapine (CLZ) is an antipsychotic which is particularly used in treatment resistant schizophrenia patients who do not respond to other agents. It is preferred because it reduces suicidal behaviours and attempts, reducing aggression and violent behaviour. The aim of the study is to evaluate the effects of ABCB1 rs1045642 and UGT1A4 rs2011425 polymorphisms on CLZ and its major metabolite N- desmethly clozapine (DCLZ) plasma concentrations in patients with schizophrenia. A total 109 of Turkish patients with schizophrenia on continually administered CLZ monotherapy were included. The plasma concentrations of CLZ and DCLZ were measured using an HPLC after liquid-liquid extraction while, transporter gene ABCB1 and phase two enzyme UGT1A4 polymorphisms were identified using PCR- RFLP method. Results showed that UGT1A4*3 polymorphism has statistically significant effects on CLZ C/D and DCLZ C/D levels in patients with sub/supra therapeutic levels while ABCB1 C3435T polymorphism has a significant effect on CLZ/DCLZ ratio among patients who have subtherapeutic levels. This study indicates the influence of genetic differences on plasma levels and highlights the importance of pharmacogenetic studies in clinic. Using the obtained results as pharmacogenetic biomarkers will help clinicians provide effective treatment in individual patients and reduce the undesirable side effects.

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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
309
审稿时长
32 days
期刊介绍: Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products. Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged. Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.
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