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伏立康唑的疗效和安全性与 CYP2C19 多态性对侵袭性真菌感染患者优化剂量方案的影响。

Efficacy and safety of voriconazole and CYP2C19 polymorphism for optimised dosage regimens in patients with invasive fungal infections.

机构信息

Department of Pharmacy, The First Affiliated Hospital of Medical College, Xi'an Jiaotong University, Xi'an 710061, China.

Department of Pharmacy, Tengzhou Central People's Hospital, Tengzhou 277500, China.

出版信息

Int J Antimicrob Agents. 2014 Nov;44(5):436-42. doi: 10.1016/j.ijantimicag.2014.07.013. Epub 2014 Aug 30.

Abstract

The aim of this study was to determine an optimum voriconazole target concentration, to study the influence of CYP2C19 gene status on metabolism of voriconazole and to identify a dose-adjustment strategy for voriconazole according to CYP2C19 polymorphism in patients with invasive fungal infections. A total of 328 voriconazole trough plasma concentrations (C(min)) were collected and monitored from 144 patients. Information on efficacy and safety was obtained. Voriconazole therapy was effective in 81.9% of patients (118/144), and 12.5% (18/144) exhibited signs of hepatotoxicity. The relationships between voriconazole C(min) and clinical response and hepatotoxicity were explored using logistic regression, and a target clinical C(min) range of 1.5-4 mg/L was identified. Values of voriconazole C(min) and the ratio of C(min) to concentration of voriconazole-N-oxide (C(min)/C(N)) of poor metabolisers (PMs) were significantly higher than extensive metabolisers and intermediate metabolisers. Model-based simulations showed that PM patients could be safely and effectively treated with 200 mg twice daily orally or intravenously, and non-PM patients with 300 mg twice daily orally or 200mg twice daily intravenously. This study highlighted that voriconazole C(min) and C(min)/C(N) are strongly influenced by CYP2C19 polymorphism, and gene-adjusted dosing is important to achieve therapeutic levels that maximise therapeutic response and minimise hepatotoxicity.

摘要

本研究旨在确定伏立康唑的最佳目标浓度,研究 CYP2C19 基因状态对伏立康唑代谢的影响,并根据侵袭性真菌感染患者 CYP2C19 多态性确定伏立康唑的剂量调整策略。共收集并监测了 144 例患者的 328 个伏立康唑谷浓度(C(min))。获得了关于疗效和安全性的信息。伏立康唑治疗在 81.9%的患者(118/144)中有效,12.5%(18/144)出现肝毒性迹象。使用逻辑回归探索了伏立康唑 C(min)与临床反应和肝毒性之间的关系,并确定了 1.5-4mg/L 的目标临床 C(min)范围。弱代谢者(PMs)的伏立康唑 C(min)值和伏立康唑-N-氧化物浓度比值(C(min)/C(N))值明显高于广泛代谢者和中间代谢者。基于模型的模拟表明,PM 患者可以安全有效地接受每日两次口服或静脉注射 200mg,非 PM 患者可以接受每日两次口服或静脉注射 300mg 或 200mg。本研究强调,伏立康唑 C(min)和 C(min)/C(N)受 CYP2C19 多态性的强烈影响,基因调整剂量对于达到最大治疗反应和最小化肝毒性的治疗水平非常重要。

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