Hypothesized pharmacogenomic and medication influences on tetrahydrocannabinol and cannabidiol metabolism in a cohort of unselected oral cannabis users.

IF 4.1 Q1 PHARMACOLOGY & PHARMACY
Jessica A Wright, Linda Huang, Basant E Katamesh, Siddhant Yadav, Abhinav Singla, Ann Vincent
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引用次数: 0

Abstract

Background: Differences in cannabinoid metabolism and patient responses can arise even with equivalent doses and formulations. Genetic polymorphisms in genes responsible for cannabinoid metabolism and medications that alter CYP450 pathways responsible for metabolism of cannabinoids may account for some of this variability.

Materials and methods: A retrospective chart review was conducted on a cohort of unselected patients who had previously completed pharmacogenomic testing and reported oral cannabis use, as defined as "oral" or "by mouth" route of administration. The objective was to identify atypical variants and medications in this cohort and formulate a hypothesis on how these variables influence the metabolism of Tetrahydrocannabinol (THC) and Cannabidiol (CBD).

Results: Oral cannabis use was confirmed in 71 patients, with an average age of 68.5 years, and primarily white women. Of the 71 patients, 10 had no atypical variants; 31 had atypical variants in CYP2C9; 37 had atypical variants in CYP2C19; 6 had atypical variants in CYP3A4; and 15 had atypical variants in CYP3A5. Of the 71 patients, 5 were taking medications that could interact with THC, and 8 were taking medications that could interact with CBD.

Conclusion: The results this study reveal the spectrum of hypothesized alterations in THC and CBD metabolism due to atypical genetic variants and medications. The absence of published clinical outcomes in this field renders it challenging to estimate clinical significance of these findings. Until such data become available, clinicians should remain aware of the possibility that atypical variants and medications may impact patients' responses to THC and CBD.

假设药物基因组学和药物对未选择的口服大麻使用者四氢大麻酚和大麻二酚代谢的影响。
背景:即使相同的剂量和配方,大麻素代谢和患者反应也可能出现差异。负责大麻素代谢的基因的遗传多态性和改变负责大麻素代谢的CYP450通路的药物可能是这种变异的部分原因。材料和方法:对一组未选择的患者进行回顾性图表回顾,这些患者先前已完成药物基因组学测试并报告口服大麻使用,定义为“口服”或“口服”给药途径。目的是确定该队列中的非典型变异和药物,并就这些变量如何影响四氢大麻酚(THC)和大麻二酚(CBD)的代谢制定假设。结果:71例患者被证实使用过口服大麻,平均年龄68.5岁,主要是白人女性。71例患者中,10例无非典型变异;31例CYP2C9有非典型变异;CYP2C19不典型变异37例;6例CYP3A4有非典型变异;15例CYP3A5有非典型变异。在71名患者中,5名患者服用的药物可能与四氢大麻酚相互作用,8名患者服用的药物可能与CBD相互作用。结论:本研究结果揭示了非典型遗传变异和药物导致的四氢大麻酚和CBD代谢的假设改变谱。该领域缺乏已发表的临床结果,因此很难估计这些发现的临床意义。在获得这些数据之前,临床医生应该意识到非典型变异和药物可能会影响患者对THC和CBD的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.20
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