抄録
Currently, combinations of typical types of antiretroviral agents have been adopted as chemotherapy for human immunodeficiency virus (HIV) infection, comprising two nucleoside analogue reverse transcriptase inhibitors plus one of a non-nucleoside reverse transcriptase inhibitor, an integrase strand-transfer inhibitor, and a protease inhibitor. Although several meta-analyses have been conducted to determine first-line combination antiretroviral therapy, this has yet to be confirmed due to the technical limitation associated. In the present study, we applied a model-based meta-analysis (MBMA) approach, because it allows integration of information from clinical trials with varying dosing, duration, and sampling time points, resulting in enlargement of available data sources. We performed a bibliographic search to identify clinical trials involving dolutegravir (DTG)-based and efavirenz (EFV)-based regimens in HIV-infected, antiretroviral therapy-naïve adults, and then identified 30 independent trial data. The time course of drug effect was described by a consecutive first-order kinetic model and analyzed using the nonlinear mixed effect modeling approach. The developed model suggests that the DTG-based regimen provides a faster-acting and more sustainable drug effect than the EFV-based regimen. Moreover, the drug effect tends to appear more slowly and decay faster in severe patients having higher viral load or smaller baseline CD4 count.
| 本文言語 | 英語 |
|---|---|
| ページ(範囲) | 687-694 |
| ページ数 | 8 |
| ジャーナル | Journal of Infection and Chemotherapy |
| 巻 | 25 |
| 号 | 9 |
| DOI | |
| 出版ステータス | 出版済み - 09-2019 |
| 外部発表 | はい |
UN SDG
この成果は、次の持続可能な開発目標に貢献しています
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SDG 3 すべての人に健康と福祉を
All Science Journal Classification (ASJC) codes
- 微生物学(医療)
- 感染症
- 薬理学(医学)
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