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环丝氨酸和利奈唑胺治疗结核性脑膜炎:潜在应用的药代动力学证据。

Cycloserine and Linezolid for Tuberculosis Meningitis: Pharmacokinetic Evidence of Potential Usefulness.

机构信息

Department of Medicine, Division of Infectious Diseases, Emory University, Atlanta, Georgia, USA.

Emory University School of Medicine, Atlanta, Georgia, USA.

出版信息

Clin Infect Dis. 2022 Sep 10;75(4):682-689. doi: 10.1093/cid/ciab992.

Abstract

BACKGROUND

The ability of antituberculosis drugs to cross the blood-brain barrier and reach the central nervous system is critical to their effectiveness in treating tuberculosis meningitis (TBM). We sought to fill a critical knowledge gap by providing data on the ability of new and repurposed antituberculosis drugs to penetrate into the cerebrospinal fluid (CSF).

METHODS

We conducted a clinical pharmacology study among patients treated for TBM in Tbilisi, Georgia, from January 2019 until January 2020. Serial serum and CSF samples were collected while patients were hospitalized. CSF was collected from routine lumbar punctures with the timing of the lumbar puncture alternating between 2 and 6 hours to capture early and late CSF penetration.

RESULTS

A total of 17 patients treated for TBM (8 with confirmed disease) were included; all received linezolid, with a subset receiving cycloserine (5), clofazimine (5), delamanid (4), and bedaquiline (2). All CSF measurements of bedaquiline (12), clofazimine (24), and delamanid (19) were below the limit of detection. The median CSF concentrations of cycloserine at 2 and 6 hours were 15.90 and 15.10 µg/mL with adjusted CSF/serum ratios of 0.52 and 0.66. CSF concentrations of linezolid were 0.90 and 3.14 µg/mL at 2 and 6 hours, with adjusted CSF/serum ratios of 0.25 and 0.59, respectively. CSF serum linezolid concentrations were not affected by rifampin coadministration.

CONCLUSIONS

Based on moderate to high CSF penetration, linezolid and cycloserine may be effective drugs for TBM treatment, whereas the utility of bedaquiline, delamanid, and clofazimine is uncertain given their low CSF penetration.

摘要

背景

抗结核药物穿透血脑屏障并到达中枢神经系统的能力对于治疗结核性脑膜炎(TBM)的有效性至关重要。我们旨在通过提供有关新型和重新利用的抗结核药物穿透脑脊液(CSF)能力的数据来填补这一关键知识空白。

方法

我们在格鲁吉亚第比利斯对接受 TBM 治疗的患者进行了一项临床药理学研究,时间为 2019 年 1 月至 2020 年 1 月。在住院期间采集了患者的血清和 CSF 连续样本。CSF 是通过常规腰椎穿刺采集的,腰椎穿刺的时间在 2 至 6 小时之间交替,以捕获早期和晚期 CSF 穿透。

结果

共纳入 17 例接受 TBM 治疗的患者(8 例为确诊病例);所有患者均接受利奈唑胺治疗,其中部分患者接受环丝氨酸(5 例)、氯法齐明(5 例)、德拉马尼(4 例)和贝达喹啉(2 例)。贝达喹啉(12 例)、氯法齐明(24 例)和德拉马尼(19 例)的所有 CSF 测量值均低于检测限。环丝氨酸在 2 小时和 6 小时时的 CSF 中位数浓度分别为 15.90 和 15.10 µg/mL,调整后的 CSF/血清比值分别为 0.52 和 0.66。利奈唑胺在 2 小时和 6 小时时的 CSF 浓度分别为 0.90 和 3.14 µg/mL,调整后的 CSF/血清比值分别为 0.25 和 0.59。利福平联合用药并未影响 CSF 血清利奈唑胺浓度。

结论

基于中度至高度 CSF 穿透性,利奈唑胺和环丝氨酸可能是治疗 TBM 的有效药物,而贝达喹啉、德拉马尼和氯法齐明的 CSF 穿透性较低,其应用价值尚不确定。

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