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CYP2B6和CYP2C19基因多态性对重度抑郁症患者舍曲林代谢的影响。

Influence of CYP2B6 and CYP2C19 polymorphisms on sertraline metabolism in major depression patients.

作者信息

Yuce-Artun Nazan, Baskak Bora, Ozel-Kizil Erguvan Tugba, Ozdemir Hatice, Uckun Zuhal, Devrimci-Ozguven Halise, Suzen Halit Sinan

机构信息

Biotechnology Institute, Ankara University, Ankara, Turkey.

School of Medicine, Psychiatry Department, Ankara University, Dikimevi, Ankara, Turkey.

出版信息

Int J Clin Pharm. 2016 Apr;38(2):388-94. doi: 10.1007/s11096-016-0259-8. Epub 2016 Jan 30.

Abstract

BACKGROUND

Genetic polymorphisms in CYP2B6 and CYP2C19 may cause variability in the metabolism of sertraline, a widely used antidepressant in major depressive disorder treatment.

OBJECTIVE

This study investigates the impact of CYP2B64 (785A > G), CYP2B69 (516G > T), CYP2B66 (516G > T + 685G > A) CYP2C192 (685G > A), CYP2C19*17 (-3402C > T) polymorphisms on plasma concentrations of sertraline and N-desmethyl sertraline in major depression patients treated with sertraline [n = 50].

SETTING

Participants were patients who admitted to an adult psychiatry outpatient unit at a university hospital. These were DSM-IV major depression diagnosed patients with a stable sertraline medication regimen [for at least one month].

METHODS

CYP2B64 (rs 2279343; 785A > G), CYP2B69 (516G > T; rs 3745274), CYP2B66 (516G > T + 685G > A) CYP2C192 (rs 4244285; 685G > A), CYP2C19*17 (rs 11188072; -3402C > T), polymorphisms were analyzed by polymerase chain reaction and restriction fragment length polymorphism. Plasma concentrations were measured by high-performance liquid chromatography in patients treated with SERT.

MAIN OUTCOME MEASURE

The distribution of CYP2B6*4, *6, 9 and CYP2C192, *17 among patient group and the association between genotype and sertraline metabolism.

RESULTS

Sertraline, N-desmethyl sertraline, N-desmethyl sertraline/sertraline and dose-adjusted plasma concentrations were statistically compared between individuals with wild-type and variant alleles both for CYP2B6 and CYP2C19 enzymes. The mean N-desmethyl sertraline/sertraline value, was significantly lower in all subgroups with *6 and *9 variant alleles (p < 0.05). Sertraline/C values were significantly higher (p < 0.05) and N-desmethyl sertraline/C values were lower in all subgroups with *6 and *9 variant alleles compared to wild-type subgroup.

CONCLUSION

CYP2B6*6 and *9 variant alleles had a significant decreasing effect on sertraline metabolism in major depression patients which might result as variations in sertraline therapy.

摘要

背景

CYP2B6和CYP2C19基因多态性可能导致舍曲林代谢存在差异,舍曲林是治疗重度抑郁症时广泛使用的一种抗抑郁药。

目的

本研究调查CYP2B64(785A>G)、CYP2B69(516G>T)、CYP2B66(516G>T+685G>A)、CYP2C192(685G>A)、CYP2C19*17(-3402C>T)基因多态性对接受舍曲林治疗的重度抑郁症患者[n=50]血浆中舍曲林和N-去甲基舍曲林浓度的影响。

背景

参与者为在一家大学医院成人精神科门诊就诊的患者。这些是诊断为DSM-IV重度抑郁症且舍曲林用药方案稳定[至少一个月]的患者。

方法

采用聚合酶链反应和限制性片段长度多态性分析法分析CYP2B64(rs 2279343;785A>G)、CYP2B69(516G>T;rs 3745274)、CYP2B66(516G>T+685G>A)、CYP2C192(rs 4244285;685G>A)、CYP2C19*17(rs 11188072;-3402C>T)基因多态性。采用高效液相色谱法测定接受舍曲林治疗患者的血浆浓度。

主要观察指标

患者组中CYP2B6*4、*6、9和CYP2C192、*17的分布情况以及基因型与舍曲林代谢之间的关联。

结果

对CYP2B6和CYP2C19酶野生型和变异等位基因个体的舍曲林、N-去甲基舍曲林、N-去甲基舍曲林/舍曲林以及剂量调整后的血浆浓度进行了统计学比较。所有携带6和9变异等位基因的亚组中,N-去甲基舍曲林/舍曲林的平均比值显著较低(p<0.05)。与野生型亚组相比,所有携带6和9变异等位基因的亚组中,舍曲林/C值显著较高(p<0.05),而N-去甲基舍曲林/C值较低。

结论

CYP2B66和9变异等位基因对重度抑郁症患者的舍曲林代谢有显著降低作用,这可能导致舍曲林治疗出现差异。

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