中度CYP2C19代谢患者舍曲林和大麻二酚药物-基因相互作用导致的低钠血症性认知功能障碍。

Jade Camara Nanan, Sheena Crosby, Michael J Schuh
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引用次数: 2

摘要

背景:药物基因组学(PGx)可以在药物-基因相互作用的临床应用中更精确地确定药物不良反应(adr)的原因。病例总结:患者是CYP2C19的中间代谢物,服用低剂量的舍曲林治疗抑郁和焦虑已有20年。在加入大麻二酚(CBD)后,患者出现低钠血症和认知障碍。提出的机制是CBD的药物-基因相互作用进一步抑制舍曲林的CYP2C19代谢,增加药物暴露,产生中度至重度低钠血症和随后的认知功能障碍。实践意义:药物基因组学(PGx)检测可以通过将药物不良反应(adr)或药物-药物相互作用与药物-基因相互作用的检测和应用相结合,帮助确定患者症状的病因。本病例显示CBD抑制CYP2C19进一步增加舍曲林暴露,通过CBD CYP2C19表型转化产生低钠血症和随后的认知功能障碍。
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Hyponatremic Cognitive Dysfunction Resulting from Drug-Drug-Gene Interaction between Sertraline and Cannabidiol in an Intermediate CYP2C19 Metabolizer Patient.

Background: Pharmacogenomics (PGx) can provide more precision in determining causation of adverse drug reactions (ADRs) from drug-drug-gene interaction clinical application. Case Summary: Patient was an intermediate CYP2C19 metabolizer on stable therapy taking a low but therapeutic dose of sertraline for depression and anxiety over a period of 20 years. The patient then became hyponatremic and cognitively impaired after addition of cannabidiol (CBD) to this sertraline regimen. The proposed mechanism was drug-drug-gene interaction of CBD further inhibiting the CYP2C19 metabolism of sertraline and increasing drug exposure to produce moderate to severe hyponatremia and subsequent cognitive dysfunction. Practice Implications: Pharmacogenomics (PGx) testing may assist in etiology of patient symptoms from adverse drug reactions (ADRs) or drug-drug interactions by combining these with detection and application of drug-gene interactions. This case shows inhibition of CYP2C19 by CBD to further increase sertraline exposure, producing hyponatremia and subsequent cognitive dysfunction through CYP2C19 phenoconversion by CBD.

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