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老年HIV感染者抗逆转录病毒药物的药代动力学,第二部分:2005年前获批的药物

Pharmacokinetics of Antiretroviral Drugs in Older People Living with HIV, Part II: Drugs Licensed Before 2005.

作者信息

Toledo Thainá, Oliveira Vanessa G, Cattani Vitória Berg, Seba Karine, Veloso Valdilea Gonçalves, Grinsztejn Beatriz, Cardoso Sandra Wagner, Torres Thiago S, Estrela Rita

机构信息

Sérgio Arouca National School of Public Health ENSP Fiocruz, Rio de Janeiro, RJ, Brazil.

Evandro Chagas National Institute of Infectious Diseases INI Fiocruz, Rio de Janeiro, Brazil.

出版信息

Clin Pharmacokinet. 2024 Dec;63(12):1655-1666. doi: 10.1007/s40262-024-01441-9. Epub 2024 Nov 14.

Abstract

BACKGROUND AND OBJECTIVE

Advances in antiretroviral therapy led to an increase in life expectancy among people living with human immunodeficiency virus (HIV). As aging is characterized by several physiological changes that can influence pharmacokinetics (PK), this systematic review aims to describe the impact of aging on the PK of antiretrovirals (ARV) approved by the Food and Drug Administration (FDA) before 2005.

METHODS

Searches were performed in BVS, EMBASE, and PubMed databases for publications until June 2024. Peer-reviewed published studies were included if they met the following criteria: adults (≥ 18 years) living with HIV; reporting at least one PK parameter or plasma concentration of any ARV approved by the US FDA before 2005 and still used in the clinic: lamivudine (3TC), emtricitabine (FTC), tenofovir disoproxil fumarate (TDF), abacavir (ABC), zidovudine (ZDV), efavirenz (EFV), nevirapine (NVP), atazanavir (ATV), lopinavir (LPV), ritonavir (RTV), tipranavir (TPV), and fosamprenavir (FPV); PK parameters stratified per age group as young (aged 18-49 years) or older (age ≥ 50 years) adults; and manuscripts published in English, Portuguese, or Spanish. All studies were evaluated for risk of bias. The review protocol was registered in the PROSPERO database (registration no. CRD42023463092).

RESULTS

Among 106 studies included, only 22 evaluated the PK of participants aged 50 years or older and only 5 studies compared the PK between young and older adults for ATV, RTV, EFV, and 3TC. Our analysis revealed an increase in minimal concentration (C) values for LPV, RTV, and ATV in older adults. While increased values of the area under the curve (AUC) and maximum concentration (C) were observed in older adults using ATV, 3TC, and FTC, no differences in PK were apparent between young and older adults for ABC and EFV, with no estimation possible for ZDV.

CONCLUSION

Exposure to 3TC, TDF, FTC, ATV, LPV, and RTV increases with age, while exposure to ABC and EFV appears to be unaffected. Despite the large quantity of data on PK in young adults, there is still a gap in knowledge about the effects of aging on the PK of these ARVs.

摘要

背景与目的

抗逆转录病毒疗法的进展使人类免疫缺陷病毒(HIV)感染者的预期寿命有所增加。由于衰老具有多种可影响药代动力学(PK)的生理变化,本系统评价旨在描述衰老对2005年前美国食品药品监督管理局(FDA)批准的抗逆转录病毒药物(ARV)药代动力学的影响。

方法

在BVS、EMBASE和PubMed数据库中进行检索,截至2024年6月的出版物。纳入的同行评审发表研究需符合以下标准:成年(≥18岁)HIV感染者;报告至少一项2005年前美国FDA批准且仍在临床使用的ARV的药代动力学参数或血浆浓度:拉米夫定(3TC)、恩曲他滨(FTC)、替诺福韦酯(TDF)、阿巴卡韦(ABC)、齐多夫定(ZDV)、依非韦伦(EFV)、奈韦拉平(NVP)、阿扎那韦(ATV)、洛匹那韦(LPV)、利托那韦(RTV)、替拉那韦(TPV)和福沙普那韦(FPV);按年龄组分层的药代动力学参数,分为年轻(18 - 49岁)或年长(≥50岁)成年人;以及以英文、葡萄牙文或西班牙文发表的手稿。对所有研究进行偏倚风险评估。该综述方案已在PROSPERO数据库注册(注册号CRD42023463092)。

结果

在纳入的106项研究中,仅22项评估了50岁及以上参与者的药代动力学,仅有5项研究比较了年轻和年长成年人在ATV、RTV、EFV和3TC方面的药代动力学。我们的分析显示,年长成年人中LPV、RTV和ATV的最低浓度(C)值增加。虽然在使用ATV、3TC和FTC的年长成年人中观察到曲线下面积(AUC)和最高浓度(C)值增加,但ABC和EFV在年轻和年长成年人之间的药代动力学无明显差异,ZDV无法进行评估。

结论

3TC、TDF、FTC、ATV、LPV和RTV的暴露量随年龄增加,而ABC和EFV的暴露量似乎不受影响。尽管有大量关于年轻成年人药代动力学的数据,但关于衰老对这些ARV药代动力学影响的知识仍存在差距。

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