作为抑郁症药物不良反应预测因子的 CYP2D6 基因分型和抑制。

IF 4.5 2区 医学 Q1 PSYCHIATRY
Amanda Holck, Marie Asp, Henrik Green, Åsa Westrin, Margareta Reis
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引用次数: 0

摘要

研究目的本研究的主要目的是研究多态 CYP2D6 基因的不同预测表型与抑郁症患者药物不良反应发生率之间的关联。次要目的是研究使用CYP2D6抑制剂是否会因表型转换而导致更多药物不良反应:2012年1月至2021年12月期间,415名抑郁障碍患者被纳入自然观察研究 "基因、抑郁和自杀"(GEN-DS),这些患者接受了二级精神科治疗,但治疗效果不佳。这些患者接受了半结构化访谈,并根据 DSM-IV 进行了诊断。患者还需完成英国UU副作用量表(UKU Side Effect Rating Scale)的自评版。所有患者均进行了 CYP2D6 基因分型,并分配了相应的预测 CYP2D6 表型:结果:在 415 名患者中,147 名有基因分型和 UKU 量表结果的患者也服用了一种或多种经 CYP2D6 代谢的药物。在这些患者中,我们没有发现任何证据表明预测的 CYP2D6 表型对药物不良反应的总负担或用 UKU 量表测量的任何特定症状领域有影响。我们还研究了使用一种或多种抑制 CYP2D6 酶作用的药物是否会导致因表型转换而报告的药物不良反应增多。尽管表型 PM 的比例从 13 例增加到了 38 例,但我们并没有发现这组患者的药物不良反应增加:我们没有发现 CYP2D6 表型可以预测抑郁症患者在自然环境中发生的药物不良反应。然而,在抗抑郁治疗中,CYP2D6基因型信息对于选择合适的药物、推荐某些药物的剂量或当患者出现严重不良反应时可能仍然很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CYP2D6 Genotyping and Inhibition as Predictors of Adverse Drug Reactions in Depressive Disorders.

Objective: The primary aim of this study was to examine the association between the different predicted phenotypes of the polymorphic CYP2D6 gene and the prevalence of adverse drug reactions in patients suffering from depressive disorders. The secondary aim was to investigate if comedication with CYP2D6 inhibitors resulted in more adverse drug reactions due to phenoconversion.

Methods: Between January 2012 and December 2021, 415 patients with a depressive disorder and insufficient treatment response in secondary psychiatric care were included in the naturalistic observational study Genes, Depression, and Suicidality (GEN-DS). The patients were subjected to a semistructured interview and diagnosed according to DSM-IV. Patients were also required to complete the self-rating version of the UKU Side Effect Rating Scale. All patients were genotyped for CYP2D6 and assigned a corresponding predicted CYP2D6 phenotype.

Results: Out of the 415 patients, 147 patients with available genotyping and UKU scale results were also prescribed 1 or more drugs metabolized by CYP2D6. We did not find any evidence of an effect of the predicted CYP2D6 phenotype on the total burden of adverse drug reactions or in any of the specific symptom domains as measured with the UKU scale among these patients. We also investigated if comedication with 1 or more substances that inhibited the effect of the CYP2D6 enzyme resulted in more reported adverse drug reactions due to phenoconversion. Even though the rate of phenotypic PMs increased from 13 to 38 patients, we did not find any support for increased adverse drug reactions in this group.

Conclusions: We did not find that CYP2D6 phenotype could predict the occurrence of adverse drug reactions in patients with depressive disorders in this naturalistic setting. However, information about CYP2D6 genotype may still be important in antidepressant treatment for the selection of appropriate drugs, for dosing recommendations of certain medications, or when the patient is suffering from severe adverse reactions.

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来源期刊
Journal of Clinical Psychiatry
Journal of Clinical Psychiatry 医学-精神病学
CiteScore
7.40
自引率
1.90%
发文量
0
审稿时长
3-8 weeks
期刊介绍: For over 75 years, The Journal of Clinical Psychiatry has been a leading source of peer-reviewed articles offering the latest information on mental health topics to psychiatrists and other medical professionals.The Journal of Clinical Psychiatry is the leading psychiatric resource for clinical information and covers disorders including depression, bipolar disorder, schizophrenia, anxiety, addiction, posttraumatic stress disorder, and attention-deficit/hyperactivity disorder while exploring the newest advances in diagnosis and treatment.
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