The Pharmacokinetic Interaction Between Metformin and the Natural Product Goldenseal Is Metformin Dose-Dependent: A Three-Arm Crossover Study in Adults With Type 2 Diabetes

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
James T. Nguyen, Christopher M. Arian, Rakshit S. Tanna, Maxey G. Cherel, Matthew E. Layton, John R. White, Kenneth E. Thummel, Mary F. Paine
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引用次数: 0

Abstract

Pharmacokinetic drug interactions can lead to unexpected changes in plasma concentrations of the object drug, potentially increasing the risk for adverse effects and/or decreasing therapeutic efficacy. The botanical product goldenseal was previously shown to decrease metformin systemic exposure in healthy adults. This three-arm, open-label, crossover clinical study assessed the pharmacokinetic goldenseal–metformin interaction in adults with type 2 diabetes stabilized on therapeutic doses of metformin (500–2550 mg daily). The aggregate pharmacokinetic data indicated no clinically meaningful interaction as determined by the metformin area under the plasma concentration-time curve (AUC) geometric mean ratio [90% confidence interval] of 0.93 [0.86–1.01] laying within the predefined no-effect range (0.80–1.25). However, metformin AUC decreased by ~20%, 14%, and 0% after goldenseal coadministration at low (500–750 mg), moderate (1000–1500 mg), and high (2000–2550 mg) metformin doses, respectively; renal clearance and half-life remained unchanged throughout. The exploratory pharmacodynamic endpoint, HbA1c, decreased on average from 6.8% to 6.5%, regardless of the effects of goldenseal on metformin pharmacokinetics. The decreasing effect of goldenseal on metformin systemic exposure with increasing metformin dose, coupled with no changes in renal excretion and elimination half-life, indicated that both the pharmacokinetic goldenseal–metformin interaction and the nonlinear absorption of metformin are governed by saturable, intestinal transport mechanism(s). The disconnect between changes in metformin systemic exposure and therapeutic effects emphasizes the need to evaluate clinical biomarkers to comprehensively assess drug interaction risks, particularly those involving natural products. Healthcare providers may consider cautioning patients about supplementing metformin pharmacotherapy with goldenseal to avoid risks for undesired changes in glycemic control.

Trial Registration: ClinicalTrials.gov identifier: NCT05081583

Abstract Image

二甲双胍和天然产物金毛之间的药代动力学相互作用是二甲双胍剂量依赖性的:一项成人2型糖尿病患者的三组交叉研究
药代动力学药物相互作用可导致目标药物的血浆浓度发生意想不到的变化,潜在地增加不良反应的风险和/或降低治疗效果。植物产品黄连以前被证明可以减少健康成人的全身二甲双胍暴露。这项三组、开放标签、交叉临床研究评估了在治疗剂量为每日500 - 2550mg的二甲双胍稳定的成人2型糖尿病患者的药代动力学。血浆浓度-时间曲线(AUC)几何平均比[90%置信区间]为0.93[0.86-1.01],处于预先设定的无效应范围(0.80-1.25)内,综合药代动力学数据显示无临床意义的相互作用。然而,在低剂量(500-750 mg)、中剂量(1000-1500 mg)和高剂量(2000-2550 mg)的黄芪共给药后,二甲双胍AUC分别下降了约20%、14%和0%;肾脏清除率和半衰期始终保持不变。探索性药效学终点HbA1c平均从6.8%降至6.5%,而不考虑黄连对二甲双胍药代动力学的影响。黄连对二甲双胍全身暴露的影响随着二甲双胍剂量的增加而降低,肾脏排泄和消除半衰期没有变化,表明黄连-二甲双胍的药代动力学相互作用和二甲双胍的非线性吸收都受可饱和的肠道转运机制控制。二甲双胍全身暴露变化与治疗效果之间的脱节强调了评估临床生物标志物以全面评估药物相互作用风险的必要性,特别是那些涉及天然产物的药物相互作用风险。医疗保健提供者可以考虑提醒患者补充二甲双胍药物治疗与黄芪,以避免风险,不希望血糖控制的变化。试验注册:ClinicalTrials.gov标识符:NCT05081583
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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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