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Significant differences in clinical outcomes between HIV-hepatitis C virus coinfected individuals with and without injection drug use history

机译:在有或没有注射吸毒史的艾滋病毒-丙型肝炎病毒合并感染患者之间,临床结局之间存在显着差异

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Objective: Studies focusing on HIV-hepatitis C virus (HCV) coinfected individuals without a history of IDU are limited. It is plausible that poorer clinical outcomes in HIVHCV coinfection are due to factors associated with IDU, not from HCV itself. This study compares HIV treatment outcomes and survival between HIV-HCV coinfected individuals with and without IDU history. Design: Observational cohort study. Methods: We analyzed data from a multisite Canadian cohort study of HIV-positive individuals initiating combination antiretroviral therapy (ART) after 1 January 2000. This analysis was restricted to 1254 participants with HCV coinfection and known IDU history. Cox proportional hazards regression was used to evaluate time from ART initiation to virologic suppression (two consecutive measures 250 copies/ml) and CD4+ cell count recovery (+100 cells/ml). In order to account for loss to follow-up (LTFU), competing risk analysis was used to evaluate time to death. Results: A total of 1254 participants (31% women) were included. During a median follow-up time of 3.8 years (interquartile range=2.1-6.2), 217 deaths were reported and 148 participants were LTFU. In adjusted multivariable analysis, individuals with IDU history were significantly less likely to achieve virologic suppression [adjusted hazard ratio (AHR)=0.78, 95% confidence interval (CI)=0.64-0.95]; marginally less likely to have CD4+ cell count recovery (AHR=0.82, 95% CI=0.66-1.00); and had a significantly higher risk of death (AHR=2.15, 95% CI=1.25-3.70). Conclusion: IDU history independently elevates risk for poorer clinical outcomes, separate from HCV coinfection. HIV-HCV coinfected persons are not homogeneous in characteristics or outcomes, suggesting care should be taken during statistical analyses if attributing poorer HIV-specific outcomes solely to HCV coinfection.
机译:目的:针对没有IDU病史的HIV-丙型肝炎病毒(HCV)共感染个体的研究有限。有可能的是,HIVHCV合并感染的临床结果较差是由与IDU相关的因素引起的,而不是由HCV本身引起的。这项研究比较了有无IDU病史的HIV-HCV合并感染个体之间的HIV治疗结果和生存率。设计:观察性队列研究。方法:我们分析了2000年1月1日后在加拿大进行联合抗逆转录病毒治疗(ART)的HIV阳性个体的多地点队列研究的数据。该分析仅限于1254名HCV合并感染和已知IDU病史的参与者。使用Cox比例风险回归来评估从抗逆转录病毒治疗开始到病毒学抑制的时间(两次连续测量250拷贝/ ml)和CD4 +细胞计数恢复(+100细胞/ ml)。为了解决后续损失(LTFU),使用竞争风险分析来评估死亡时间。结果:总共包括1254名参与者(31%为女性)。在中位随访时间3.8年(四分位间距= 2.1-6.2)期间,报告了217例死亡,其中148例为LTFU。在调整后的多变量分析中,具有IDU病史的个体实现病毒学抑制的可能性大大降低[调整后的危险比(AHR)= 0.78,95%置信区间(CI)= 0.64-0.95];几乎没有CD4 +细胞计数恢复的可能性(AHR = 0.82,95%CI = 0.66-1.00);并且具有更高的死亡风险(AHR = 2.15,95%CI = 1.25-3.70)。结论:与HCV合并感染不同,IDU病史独立增加临床结果较差的风险。 HIV-HCV合并感染者的特征或结局不均一,建议如果仅将较差的HIV特异性结果仅归因于HCV合并感染,则应在统计分析期间应谨慎。

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