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不同的伴随抗逆转录病毒药物对多替拉韦谷浓度的影响。

Different effects of the companion antiretroviral drugs on dolutegravir trough concentrations.

机构信息

Department of Infectious Diseases.

Gestione Ambulatoriale Politerapie (GAP) Outpatient Clinic, ASST Fatebenefratelli Sacco University Hospital, Milan, Italy.

出版信息

AIDS. 2024 May 1;38(6):847-851. doi: 10.1097/QAD.0000000000003843. Epub 2024 Jan 15.

Abstract

BACKGROUND

Dolutegravir is widely used in different dual and triple antiretroviral regimens. Here, we sought to investigate the effect of the companion antiretroviral drug(s) on dolutegravir plasma trough concentrations in persons with HIV, with a focus on dual regimens.

METHODS

Dolutegravir concentrations collected from October 2015 to March 2023 ( n  = 900) were stratified according to the main antiretroviral classes (NRTIs, NNRTIs, protease inhibitors) and according to single drugs. Dolutegravir concentrations measured in persons with HIV concomitantly treated with lamivudine were considered as the reference group.

RESULTS

Dolutegravir trough concentrations were significantly higher in persons with HIV given protease inhibitors compared with the reference [1886 (1036-2940) versus 1575 (1026-2226) ng/ml; P  = 0.004]. The highest dolutegravir concentrations were measured in persons with HIV concomitantly treated with unboosted atazanavir [2908 (2130-4135) ng/ml]. Conversely, co-administration of darunavir/ritonavir resulted in significantly lower dolutegravir exposure [909 (496-1397) ng/ml; P  = 0.002 versus reference]. Among NNRTIs, the higher dolutegravir concentrations were measured in presence of rilpivirine [2252 (1489-2686); P  < 0.001 versus reference].

CONCLUSION

Dolutegravir trough concentrations are differently affected by individual antiretroviral drugs, with some drug combinations (i.e. dolutegravir/darunavir/cobicistat, or dolutegravir/rilpivirine) providing significantly higher than expected dolutegravir exposure. Such combinations might be advantageous when there are concerns about dolutegravir plasma exposure or resistance.

摘要

背景

多替拉韦在不同的二联和三联抗逆转录病毒方案中被广泛应用。在此,我们旨在研究伴随抗逆转录病毒药物对艾滋病毒感染者多替拉韦血药谷浓度的影响,重点关注二联方案。

方法

根据主要抗逆转录病毒类别(核苷逆转录酶抑制剂、非核苷逆转录酶抑制剂、蛋白酶抑制剂)和单一药物对 2015 年 10 月至 2023 年 3 月收集的多替拉韦浓度进行分层。同时接受拉米夫定治疗的艾滋病毒感染者的多替拉韦浓度被视为参考组。

结果

与参考组[1886(1036-2940)ng/ml]相比,同时接受蛋白酶抑制剂治疗的艾滋病毒感染者的多替拉韦血药谷浓度显著升高[1575(1026-2226)ng/ml;P=0.004]。同时接受未增强阿扎那韦治疗的艾滋病毒感染者的多替拉韦浓度最高[2908(2130-4135)ng/ml]。相反,同时接受达鲁那韦/利托那韦治疗会导致多替拉韦暴露显著降低[909(496-1397)ng/ml;P=0.002 与参考组相比]。在非核苷逆转录酶抑制剂中,同时接受利匹韦林治疗的多替拉韦浓度更高[2252(1489-2686);P<0.001 与参考组相比]。

结论

多替拉韦血药谷浓度受个体抗逆转录病毒药物的影响不同,一些药物组合(即多替拉韦/达鲁那韦/考比司他,或多替拉韦/利匹韦林)提供的多替拉韦暴露水平显著高于预期。当存在多替拉韦血浆暴露或耐药性的担忧时,这些组合可能是有利的。

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