Lima Viviane D, Kretz Patricia, Palepu Anita, Bonner Simon, Kerr Thomas, Moore David, Daniel Mark, Montaner Julio S G, Hogg Robert S
British Columbia Centre for Excellence in HIV/AIDS, St, Paul's Hospital, Vancouver, Canada.
AIDS Res Ther. 2006 May 24;3:14. doi: 10.1186/1742-6405-3-14.
Although the impact of Aboriginal status on HIV incidence, HIV disease progression, and access to treatment has been investigated previously, little is known about the relationship between Aboriginal ethnicity and outcomes associated with highly active antiretroviral therapy (HAART). We undertook the present analysis to determine if Aboriginal and non-Aboriginal persons respond differently to HAART by measuring HIV plasma viral load response, CD4 cell response and time to all-cause mortality.
A population-based analysis of a cohort of antiretroviral therapy naïve HIV-positive Aboriginal men and women 18 years or older in British Columbia, Canada. Participants were antiretroviral therapy naïve, initiated triple combination therapy between August 1, 1996 and September 30, 1999. Participants had to complete a baseline questionnaire as well as have at least two follow-up CD4 and HIV plasma viral load measures. The primary endpoints were CD4 and HIV plasma viral load response and all cause mortality. Cox proportional hazards models were used to determine the association between Aboriginal status and CD4 cell response, HIV plasma viral load response and all-cause mortality while controlling for several confounder variables.
A total of 622 participants met the study criteria. Aboriginal status was significantly associated with no AIDS diagnosis at baseline (p = 0.0296), having protease inhibitor in the first therapy (p = 0.0209), lower baseline HIV plasma viral load (p < 0.001), less experienced HIV physicians (P = 0.0133), history of IDU (p < 0.001), not completing high school (p = 0.0046), and an income of less than $10,000 per year (p = 0.0115). Cox proportional hazards models controlling for clinical characteristics found that Aboriginal status had an increased hazard of mortality (HR = 3.12, 95% CI: 1.77-5.48) but did not with HIV plasma viral load response (HR = 1.15, 95% CI: 0.89-1.48) or CD4 cell response (HR = 0.95, 95% CI: 0.73-1.23).
Our study demonstrates that HIV-infected Aboriginal persons accessing HAART had similar HIV treatment response as non-Aboriginal persons but have a shorter survival. This study highlights the need for continued research on medical interventions and behavioural changes among HIV-infected Aboriginal and other marginalized populations.
尽管之前已对原住民身份对艾滋病毒发病率、艾滋病毒疾病进展及治疗可及性的影响进行了研究,但对于原住民种族与高效抗逆转录病毒疗法(HAART)相关结局之间的关系却知之甚少。我们进行了本分析,通过测量艾滋病毒血浆病毒载量反应、CD4细胞反应及全因死亡时间,以确定原住民和非原住民对HAART的反应是否存在差异。
对加拿大不列颠哥伦比亚省18岁及以上未接受过抗逆转录病毒治疗的艾滋病毒阳性原住民男女队列进行基于人群的分析。参与者均未接受过抗逆转录病毒治疗,于1996年8月1日至1999年9月30日开始接受三联联合治疗。参与者必须完成一份基线调查问卷,且至少有两次随访的CD4和艾滋病毒血浆病毒载量测量值。主要终点为CD4和艾滋病毒血浆病毒载量反应及全因死亡。使用Cox比例风险模型来确定原住民身份与CD4细胞反应、艾滋病毒血浆病毒载量反应及全因死亡之间的关联,同时控制几个混杂变量。
共有622名参与者符合研究标准。原住民身份与基线时未诊断出艾滋病显著相关(p = 0.0296)、首次治疗中使用蛋白酶抑制剂(p = 0.0209)、基线艾滋病毒血浆病毒载量较低(p < 0.001)、经验较少的艾滋病毒医生(P = 0.0133)、注射吸毒史(p < 0.001)、未完成高中学业(p = 0.0046)以及年收入低于10,000美元(p = 0.0115)相关。控制临床特征的Cox比例风险模型发现,原住民身份有更高的死亡风险(HR = 3.12,95% CI:1.77 - 5.48),但与艾滋病毒血浆病毒载量反应(HR = 1.15,95% CI:0.89 - 1.48)或CD4细胞反应(HR = 0.95,95% CI:0.73 - 1.23)无关。
我们的研究表明,接受HAART治疗的艾滋病毒感染原住民与非原住民有相似的艾滋病毒治疗反应,但生存期较短。本研究强调了对艾滋病毒感染的原住民及其他边缘化人群的医学干预和行为改变持续进行研究的必要性。