McCance-Katz E F, Rainey P M, Jatlow P, Friedland G
Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, USA.
J Acquir Immune Defic Syndr Hum Retrovirol. 1998 Aug 15;18(5):435-43. doi: 10.1097/00042560-199808150-00004.
Large numbers of injection drug users (IDUs) are infected with HIV and receive both methadone and zidovudine (ZDV) therapy. Pharmacokinetic interactions between these agents may effect drug efficacy, toxicity, and compliance. To confirm and expand previous studies that identified a potential interaction between ZDV and methadone, we performed a within-subject study to determine oral and intravenous ZDV pharmacokinetics in 8 recently detoxified, heroin-addicted patients with HIV disease before and after initiation of methadone treatment. Acute methadone treatment increased oral ZDV in the area under the curve (AUC) by 41% (p = .03) and intravenous ZDV AUC by 19% (p = .06). Clearance was reduced by 21% (p = .007) and 19% (p = .04), respectively. Chronic methadone treatment increased oral ZDV AUC by 29% (p = .15) and intravenous ZDV AUC by 41% (p = .05). Clearance was decreased by 26% for both routes (p = .02). Methadone levels remained in the therapeutic range during ZDV treatment. These effects resulted primarily from inhibition of ZDV glucuronidation, but also from decreased renal clearance of ZDV. This study confirms that methadone-maintained patients receiving standard ZDV doses experience greater ZDV exposure and may be at increased risk for ZDV side effects and toxicity. Increased toxicity surveillance and possibly reduction in ZDV dose are indicated when these two agents are given concomitantly.
大量注射吸毒者感染了艾滋病毒,并接受美沙酮和齐多夫定(ZDV)治疗。这些药物之间的药代动力学相互作用可能会影响药物疗效、毒性和依从性。为了证实并扩展先前确定ZDV与美沙酮之间存在潜在相互作用的研究,我们进行了一项自身对照研究,以确定8名近期戒毒的艾滋病毒感染海洛因成瘾患者在开始美沙酮治疗前后口服和静脉注射ZDV的药代动力学。急性美沙酮治疗使口服ZDV的曲线下面积(AUC)增加了41%(p = 0.03),静脉注射ZDV的AUC增加了19%(p = 0.06)。清除率分别降低了21%(p = 0.007)和19%(p = 0.04)。慢性美沙酮治疗使口服ZDV的AUC增加了29%(p = 0.15),静脉注射ZDV的AUC增加了41%(p = 0.05)。两种给药途径的清除率均降低了26%(p = 0.02)。在ZDV治疗期间,美沙酮水平保持在治疗范围内。这些影响主要是由于ZDV葡萄糖醛酸化受到抑制,但也源于ZDV肾脏清除率降低。本研究证实,接受标准ZDV剂量的美沙酮维持治疗患者会有更高的ZDV暴露量,可能会增加出现ZDV副作用和毒性的风险。当同时给予这两种药物时,需要加强毒性监测,并可能需要降低ZDV剂量。