Wright Jessica A, Huang Linda, Katamesh Basant E, Yadav Siddhant, Singla Abhinav, Vincent Ann
Pharmacy Services, Mayo Clinic College of Medicine and Science, 200 First St SW, Rochester, MN, 55905, USA.
Division of General Internal Medicine, Mayo Clinic College of Medicine and Science, 200 First St SW, Rochester, MN, 55905, USA.
J Cannabis Res. 2025 Jan 4;7(1):1. doi: 10.1186/s42238-024-00256-6.
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.
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).
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.
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.
即使使用等效剂量和制剂,大麻素代谢及患者反应仍可能存在差异。负责大麻素代谢的基因中的遗传多态性以及改变负责大麻素代谢的细胞色素P450途径的药物可能是造成这种变异性的部分原因。
对一组未经挑选的患者进行回顾性病历审查,这些患者此前已完成药物基因组学检测并报告有口服大麻使用情况,口服大麻使用定义为“口服”给药途径。目的是识别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)的代谢提出假设。
71名患者被证实有口服大麻使用情况,平均年龄68.5岁,主要为白人女性。在这71名患者中,10名没有非典型变异;31名在CYP2C9中有非典型变异;37名在CYP2C19中有非典型变异;6名在CYP3A4中有非典型变异;15名在CYP3A5中有非典型变异。在这71名患者中,5名正在服用可能与THC相互作用的药物,8名正在服用可能与CBD相互作用的药物。
本研究结果揭示了由于非典型基因变异和药物导致的THC和CBD代谢中假设改变的范围。该领域缺乏已发表的临床结果,使得评估这些发现的临床意义具有挑战性。在获得此类数据之前,临床医生应始终意识到非典型变异和药物可能影响患者对THC和CBD反应的可能性。