意大利和美国艾滋病毒血清转换注射吸毒者到艾滋病和传染病死亡时间的直接比较:ALIVE和ISS研究的结果。艾滋病与静脉注射的联系。意大利血清转化研究。

P Pezzotti, N Galai, D Vlahov, G Rezza, C M Lyles, J Astemborski
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引用次数: 56

摘要

目的:比较多种药物注射者(艾滋病与静脉注射经历的联系[ALIVE]研究)与主要使用阿片类药物注射者(意大利血清转化研究[ISS])的HIV疾病进展率。设计:对血清转化(SC)日期已知的hiv阳性个体进行前瞻性队列研究。ALIVE研究涉及美国一个以社区为基础的注射吸毒者(IDU)队列,ISS报告了意大利一个以临床为基础的不同HIV暴露方式的注射吸毒者队列。方法:将两个队列的数据进行合并。SC的日期被估计为最后一次阴性和第一次阳性HIV检测之间的时间中点。使用了事件时间(即艾滋病或传染病死亡)统计方法。进展为事件的相对危险度(RH)根据SC年龄、性别和SC年份进行调整。结果:1003例IDUs(251例来自ALIVE, 752例来自ISS)中,226例进展为艾滋病,146例死于艾滋病或感染性疾病;其中10人没有被诊断出患有艾滋病。两组注射者在SC时的年龄(中位数,ALIVE组为35岁,ISS组为25岁)、女性比例(24%对31%)、种族(7.6%对100%白人)和血清转化年份(即ISS参与者的血清转化平均早于ALIVE参与者)方面存在差异。虽然单变量分析提示在队列之间进展为艾滋病或因传染病死亡的可能差异,但调整年龄的多变量分析显示,在队列、性别、种族或血清转化时间方面没有显著差异。25岁患者到艾滋病的中位时间ALIVE组为12.3年,ISS组为11.8年;对于35岁的人来说,分别是8.5年和8.2年。这些估计值与在国际空间站观察到的非注射吸毒者的估计值和从大量同性恋男性中观察到的估计值相似。结论:我们的研究结果证实了在考虑HIV感染潜伏期时考虑年龄因素的重要性。尽管药物使用特征存在差异,但在两个注射吸毒者队列之间以及注射吸毒者和非注射吸毒者之间,每个年龄段的艾滋病中位数时间相似,这表明注射吸毒对艾滋病毒进展的影响可以忽略不计。
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Direct comparison of time to AIDS and infectious disease death between HIV seroconverter injection drug users in Italy and the United States: results from the ALIVE and ISS studies. AIDS Link to Intravenous Experiences. Italian Seroconversion Study.

Objective: To compare the rate of HIV disease progression in a sample of polydrug injectors (AIDS Link to Intravenous Experiences [ALIVE] study) with that in a sample of predominantly opiate injectors (Italian Seroconversion Study [ISS]).

Design: Prospective cohort studies of HIV-positive individuals whose date of seroconversion (SC) is known with a good degree of precision. The ALIVE study involves a community-based cohort of injection drug users (IDU) in the United States and the ISS reports on a clinic-based cohort of seroconverters in Italy with different exposure modalities to HIV.

Methods: Data from the two cohorts were combined. The date of SC was estimated as the midpoint in time between the last negative and the first positive HIV test. Time-to-event (i.e., AIDS or death from an infectious disease) statistical methods were used. Relative hazards (RH) of progression to event were adjusted by age at SC, gender, and year of SC.

Results: Of the 1003 IDUs (251 from ALIVE and 752 from ISS), 226 progressed to AIDS, and 146 died after AIDS or from an infectious disease; of these, 10 were without an AIDS diagnosis. The two groups of IDUs differed in terms of age at SC (median, 35 years for ALIVE and 25 years for ISS), proportion of women (24% versus 31%), race (7.6% versus 100% white), and year of seroconversion (i.e., ISS participants seroconverted, on average, earlier than ALIVE participants). Although the univariate analysis suggested possible differences for progression to AIDS, or to death from infectious disease between cohorts, multivariate analyses that adjusted for age showed no significant differences by cohort, gender, race, or time of seroconversion. The median time to AIDS for 25-year-old persons was 12.3 years for ALIVE and 11.8 years for ISS; for 35-year-old persons, it was 8.5 and 8.2 years, respectively. These estimates were similar to those for non-IDUs observed in the ISS and to those from large cohort of homosexual men.

Conclusion: Our results confirm the importance of accounting for age when considering the incubation period for HIV infection. Despite differences in drug use characteristics, the similar median times to AIDS, for each age, between the two cohorts of IDUs and between the IDUs and the non-IDUs suggest a negligible effect of injection drug use on HIV progression.

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