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在 HIV 阳性个体中,依非韦伦的血浆浓度与体重相关。

Plasma concentrations of efavirenz are associated with body weight in HIV-positive individuals.

机构信息

School of Medicine, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.

出版信息

J Antimicrob Chemother. 2011 Nov;66(11):2601-4. doi: 10.1093/jac/dkr360. Epub 2011 Sep 2.

Abstract

BACKGROUND

Efavirenz is among the most widely used antiretroviral drugs. Increased efavirenz exposure has been associated with CNS side effects and also with the chance of emergence of resistance upon treatment interruptions. The objective of this study was to evaluate factors associated with efavirenz plasma concentrations in a cohort of HIV-infected individuals.

METHODS

From July 2009 to March 2010, HIV-infected patients with efavirenz as part of antiretroviral therapy (600 mg at night), undetectable viral load for at least 1 year and CD4 cell count >200 cells/mm(3) were consecutively enrolled at the HIV/AIDS ambulatory care unit in southern Brazil. Plasma samples were taken 18-23 h after efavirenz last dose and analysed by validated ultra-performance liquid chromatography.

RESULTS

Forty-one subjects were included (21 females). Mean age and weight were 45.4 years and 70.9 kg, respectively. Mean efavirenz plasma concentration was 2.20 ± 2.17 mg/L. Most plasma concentrations (73%) were within the therapeutic window (1-4 mg/L); 17% were below and 10% above the limits. There were no significant associations between efavirenz concentration and age, CD4 cell count, time on antiretroviral treatment and gender. There was significant and inverse correlation between efavirenz concentrations and body weight (P = 0.013) and body mass index (P = 0.001).

CONCLUSIONS

In this cohort of well-controlled HIV-positive individuals, patients with lower weight or body mass index had a higher chance of presenting elevated plasma concentrations of efavirenz. Therapeutic drug monitoring to adjust dose might be a helpful tool to decrease efavirenz dose in order to minimize costs and adverse effects.

摘要

背景

依非韦伦是最广泛使用的抗逆转录病毒药物之一。依非韦伦暴露量增加与中枢神经系统副作用以及治疗中断时出现耐药的可能性有关。本研究的目的是评估与 HIV 感染者队列中依非韦伦血浆浓度相关的因素。

方法

2009 年 7 月至 2010 年 3 月,巴西南部 HIV/AIDS 门诊连续纳入了接受含依非韦伦(晚上 600mg)的抗逆转录病毒治疗、病毒载量至少 1 年未检出且 CD4 细胞计数>200 个/立方毫米的 HIV 感染患者。在依非韦伦最后一次给药后 18-23 小时采集血浆样本,并用经过验证的超高效液相色谱法进行分析。

结果

共纳入 41 例患者(21 例女性)。平均年龄和体重分别为 45.4 岁和 70.9kg。平均依非韦伦血浆浓度为 2.20±2.17mg/L。大多数(73%)血浆浓度处于治疗窗(1-4mg/L)内;17%低于下限,10%高于上限。依非韦伦浓度与年龄、CD4 细胞计数、抗逆转录病毒治疗时间和性别之间无显著相关性。依非韦伦浓度与体重(P=0.013)和体重指数(P=0.001)呈显著负相关。

结论

在这个 HIV 阳性患者控制良好的队列中,体重或体重指数较低的患者出现依非韦伦血浆浓度升高的可能性更高。进行治疗药物监测以调整剂量可能是一种有用的工具,可以减少依非韦伦剂量,从而降低成本和不良反应的风险。

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