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Effect of ageing on antiretroviral drug pharmacokinetics using clinical data combined with modelling and simulation

机译:老化对抗逆转录病毒药代动力学使用临床数据的影响和模拟

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Aims The impact of ageing on antiretroviral pharmacokinetics remains uncertain, leading to missing dosing recommendations for elderly people living with human immunodeficiency virus (HIV: PLWH). The objective of this study was to investigate whether ageing leads to clinically relevant pharmacokinetic changes of antiretrovirals that would support a dose adjustment based on the age of the treated PLWH. Methods Plasma concentrations for 10 first-line antiretrovirals were obtained in PLWH >= 55 years, participating in the Swiss HIV Cohort Study, and used to proof the predictive performance of our physiologically based pharmacokinetic (PBPK) model. The verified PBPK model predicted the continuous effect of ageing on HIV drug pharmacokinetics across adulthood (20-99 years). The impact of ethnicity on age-related pharmacokinetic changes between whites and other races was statistically analysed. Results Clinically observed concentration-time profiles of all investigated antiretrovirals were generally within the 95% confidence interval of the PBPK simulations, demonstrating the predictive power of the modelling approach used. The predicted decline in drug clearance drove age-related pharmacokinetic changes of antiretrovirals, resulting in a maximal 70% [95% confidence interval: 40%, 120%] increase in antiretrovirals exposure across adulthood. Peak concentration, time to peak concentration and apparent volume of distribution were predicted to be unaltered by ageing. There was no statistically significant difference of age-related pharmacokinetic changes between studied ethnicities. Conclusion Dose adjustment for antiretrovirals based on the age of male and female PLWH isa priorinot necessary in the absence of severe comorbidities considering the large safety margin of the current first-line HIV treatments.
机译:目的:老龄化对抗逆转录病毒药代动力学的影响仍然不确定,导致缺少对感染人类免疫缺陷病毒(HIV:PLWH)的老年人的剂量建议。本研究的目的是调查衰老是否会导致抗逆转录病毒药物的临床相关药代动力学变化,从而支持根据治疗PLWH的年龄进行剂量调整。方法在PLWH≥55年期间,参与瑞士HIV队列研究,获得10种一线抗逆转录病毒药物的血浆浓度,并用于证明我们基于生理的药代动力学(PBPK)模型的预测性能。经验证的PBPK模型预测了老龄化对整个成年期(20-99岁)HIV药物药代动力学的持续影响。对白人和其他种族之间种族对年龄相关药代动力学变化的影响进行了统计分析。结果所有研究抗逆转录病毒药物的临床观察浓度-时间曲线通常在PBPK模拟的95%置信区间内,证明了所用建模方法的预测能力。预期的药物清除率下降导致抗逆转录病毒药物的年龄相关药代动力学变化,导致整个成年期抗逆转录病毒药物暴露量最大增加70%[95%置信区间:40%,120%]。峰值浓度、峰值时间和表观分布体积预计不会因老化而改变。研究种族之间年龄相关的药代动力学变化无统计学显著差异。结论考虑到目前一线HIV治疗的较大安全边际,在没有严重共病的情况下,根据男性和女性PLWH的年龄调整抗逆转录病毒药物的剂量是不必要的。

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