Population pharmacokinetics of amodiaquine and piperaquine in African pregnant women with uncomplicated Plasmodium falciparum infections

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Junjie Ding, Richard M. Hoglund, Harry Tagbor, Halidou Tinto, Innocent Valéa, Victor Mwapasa, Linda Kalilani-Phiri, Jean-Pierre Van Geertruyden, Michael Nambozi, Modest Mulenga, Sebastian Hachizovu, Raffaella Ravinetto, Umberto D'Alessandro, Joel Tarning
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Abstract

Artemisinin-based combination therapy (ACT) is the first-line recommended treatment for uncomplicated malaria. Pharmacokinetic (PK) properties in pregnant women are often based on small studies and need to be confirmed and validated in larger pregnant patient populations. This study aimed to evaluate the PK properties of amodiaquine and its active metabolite, desethylamodiaquine, and piperaquine in women in their second and third trimester of pregnancy with uncomplicated P. falciparum infections. Eligible pregnant women received either artesunate-amodiaquine (200/540 mg daily, n = 771) or dihydroartemisinin-piperaquine (40/960 mg daily, n = 755) for 3 days (NCT00852423). Population PK properties were evaluated using nonlinear mixed-effects modeling, and effect of gestational age and trimester was evaluated as covariates. 1071 amodiaquine and 1087 desethylamodiaquine plasma concentrations, and 976 piperaquine plasma concentrations, were included in the population PK analysis. Amodiaquine concentrations were described accurately with a one-compartment disposition model followed by a two-compartment disposition model of desethylamodiaquine. The relative bioavailability of amodiaquine increased with gestational age (1.25% per week). The predicted exposure to desethylamodiaquine was 2.8%–32.2% higher in pregnant women than that reported in non-pregnant women, while day 7 concentrations were comparable. Piperaquine concentrations were adequately described by a three-compartment disposition model. Neither gestational age nor trimester had significant impact on the PK of piperaquine. The predicted exposure and day 7 concentrations of piperaquine were similar to that reported in non-pregnant women. In conclusion, the exposure to desethylamodiaquine and piperaquine was similar to that in non-pregnant women. Dose adjustment is not warranted for women in their second and their trimester of pregnancy.

Abstract Image

感染无并发症恶性疟原虫的非洲孕妇体内阿莫地喹和哌喹的群体药代动力学。
青蒿素类复方疗法(ACT)是治疗无并发症疟疾的一线推荐疗法。孕妇的药代动力学(PK)特性通常基于小型研究,需要在更大的孕妇群体中进行确认和验证。本研究旨在评估阿莫地喹及其活性代谢物去甲阿莫地喹和哌喹在感染无并发症恶性疟原虫的第二和第三孕期妇女中的药代动力学特性。符合条件的孕妇接受青蒿琥酯-阿莫地喹(每天 200/540 毫克,n = 771)或双氢青蒿素-哌喹(每天 40/960 毫克,n = 755)治疗 3 天(NCT00852423)。使用非线性混合效应模型评估了人群 PK 特性,并将胎龄和孕期的影响作为协变量进行了评估。1071例阿莫地喹和1087例去乙基阿莫地喹血浆浓度以及976例哌喹血浆浓度被纳入人群PK分析。阿莫地喹的浓度用一室处置模型进行了精确描述,随后又用去甲阿莫地喹的二室处置模型进行了精确描述。阿莫地喹的相对生物利用度随孕龄的增加而增加(每周增加 1.25%)。据预测,孕妇的去甲阿莫地喹暴露量比非孕妇高出 2.8%-32.2%,而第 7 天的浓度相当。哌喹的浓度可通过三室处置模型进行充分描述。妊娠年龄和孕期对哌喹的 PK 均无显著影响。哌喹的预测暴露量和第7天的浓度与非孕妇的报告相似。总之,去甲阿莫地喹和哌喹的暴露量与非妊娠妇女相似。妊娠中期和妊娠三个月的妇女无需调整剂量。
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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来源期刊
CiteScore
5.00
自引率
11.40%
发文量
146
审稿时长
8 weeks
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