Boesecke Christoph, Cooper David A
National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, Sydney NSW 2010, Australia.
Curr Opin HIV AIDS. 2008 Nov;3(6):653-9. doi: 10.1097/COH.0b013e328312c392.
To review recent studies reporting toxicity, adverse events, side effects, and drug-drug interactions related to the use of HIV protease inhibitors, with particular focus on possible clinical implications.
Toxicity-associated adverse events still remain a major concern when prescribing HIV protease inhibitors. Among those, diarrhea, lipid, and liver enzyme elevations are predominant. Also, with protease inhibitors being metabolized by the hepatic cytochrome P450, a significant number of drug-drug interactions has to be taken into account in patients who often require coadministration of drugs to treat supplementary diseases, for example, tuberculosis. Hence, scientific interest in this area continues to be high, especially in characterizing individual toxicities of particular protease inhibitors as well as in comparing them among each other.
Protease inhibitors are still a cornerstone of combination antiretroviral therapy. A profound knowledge of the unwanted, but manageable, effects of protease inhibitor therapy is required to maintain an otherwise efficient and well tolerated antiretroviral therapy. Further research will elucidate the potential role of protease inhibitors both in double-boosted salvage therapy and in resource-limited settings.
回顾近期有关与使用HIV蛋白酶抑制剂相关的毒性、不良事件、副作用及药物相互作用的研究,特别关注其可能的临床意义。
在开具HIV蛋白酶抑制剂处方时,与毒性相关的不良事件仍是主要关注点。其中,腹泻、血脂和肝酶升高最为常见。此外,由于蛋白酶抑制剂由肝细胞色素P450代谢,对于常需联合用药治疗其他疾病(如结核病)的患者,必须考虑大量的药物相互作用。因此,该领域的科学关注度持续较高,尤其是在明确特定蛋白酶抑制剂的个体毒性以及相互比较方面。
蛋白酶抑制剂仍是联合抗逆转录病毒治疗的基石。要维持高效且耐受性良好的抗逆转录病毒治疗,需要深入了解蛋白酶抑制剂治疗的不良但可控制的效应。进一步的研究将阐明蛋白酶抑制剂在双重强化挽救治疗和资源有限环境中的潜在作用。