探索东亚人与白种人的药代动力学差异:健康受试者药代动力学研究的启示。

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Translational and Clinical Pharmacology Pub Date : 2024-09-01 Epub Date: 2024-09-30 DOI:10.12793/tcp.2024.32.e15
Yoonjin Kim, Sungyeun Bae, Woo Kyung Chung, Jihoon Kwon, Ildae Song, SeungHwan Lee
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引用次数: 0

摘要

药物代谢动力学的种族间差异是环境、遗传和人口因素复杂相互作用的结果。由于潜在因素的多方面作用,确定药代动力学的种族差异具有挑战性。为了应对这些挑战,本文回顾了 9 项符合以下标准的药代动力学研究:(A) 2013 年至 2022 年期间在首尔大学医院进行的单中心研究。(B) 同时涉及东亚人(韩国人、日本人或中国人)和白种人的药代动力学研究。(C) 研究药物为口服给药。(D) 提供原始数据以供重新分析。这项回顾性分析旨在研究药物暴露中是否存在种族差异,并了解导致这些差异的可能因素。分析了药代动力学、人口统计学和临床实验室检测数据,以评估东亚人和白种人之间潜在的药代动力学差异。评估包括计算剂量归一化的时间-浓度曲线下面积(AUC)的几何平均比、剂量和体重归一化的 AUC 及其 90% 置信区间。此外,还从研究手册或相关国家的药品标签中收集了药理学信息,包括代谢途径。在 9 项研究中,有 4 项研究表明东亚人的药物暴露量比白种人高出约 1.3 至 1.8 倍。这些药物主要通过肝脏代谢排出体外,尿液中未作改变的排泄量不足 5%。两种药物通过肝细胞色素 P450 3A4 代谢,一种通过谷胱甘肽 S 转移酶代谢,另一种药物的具体代谢途径尚未确定。需要进一步开展研究,以评估这些药物的种族差异原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploration of pharmacokinetic differences between East Asians and Caucasians: insights from pharmacokinetic studies in healthy subjects.

Interethnic differences in the pharmacokinetics of drugs result from a complex interplay of environmental, genetic, and demographic factors. Identifying ethnic differences in pharmacokinetics is challenging due to the multifaceted contributions of the underlying factors. To address these challenges, this paper reviews 9 pharmacokinetic studies meeting the following criteria: (A) Conducted at Seoul National University Hospital from 2013 to 2022 as a single-center study. (B) Pharmacokinetic studies involving both East Asians (Korean, Japanese, or Chinese) and Caucasians. (C) Study drugs were administered orally. (D) Raw data was provided for reanalysis. This retrospective analysis aimed to investigate the existence of ethnic differences in drug exposure and understand the possible factors contributing to these variabilities. Pharmacokinetic, demographic, and clinical laboratory test data were analyzed to assess potential pharmacokinetic differences between East Asians and Caucasians. This assessment involved calculating the geometric mean ratio of dose-normalized area under the time-concentration curve (AUC) and dose- and weight-normalized AUC, along with their 90% confidence intervals. Additionally, pharmacological information, including metabolic pathways, was gathered from the investigational brochure or the respective country's drug label. Among 9 studies, 4 studies demonstrated approximately 1.3 to 1.8 times higher drug exposure in East Asians compared to Caucasians. These drugs were primarily eliminated through hepatic metabolism, with less than 5% excreted unchanged in the urine. Two drugs were metabolized by hepatic cytochrome P450 3A4, one by glutathione S-transferase, and specific metabolic pathways for another drug were not identified. Further research is needed to assess the causes of ethnic variability in these drugs.

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来源期刊
Translational and Clinical Pharmacology
Translational and Clinical Pharmacology Medicine-Pharmacology (medical)
CiteScore
1.60
自引率
11.10%
发文量
17
期刊介绍: Translational and Clinical Pharmacology (Transl Clin Pharmacol, TCP) is the official journal of the Korean Society for Clinical Pharmacology and Therapeutics (KSCPT). TCP is an interdisciplinary journal devoted to the dissemination of knowledge relating to all aspects of translational and clinical pharmacology. The categories for publication include pharmacokinetics (PK) and drug disposition, drug metabolism, pharmacodynamics (PD), clinical trials and design issues, pharmacogenomics and pharmacogenetics, pharmacometrics, pharmacoepidemiology, pharmacovigilence, and human pharmacology. Studies involving animal models, pharmacological characterization, and clinical trials are appropriate for consideration.
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