Abstract

BackgroundAlthough 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.MethodsA 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.ResultsA 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).ConclusionOur 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.

Highlights

  • There are trends for global health concerns to have a greater impact on ethnic minorities [1,2,3,4,5]

  • American Indians and Alaska Natives make up 6% of all new human immunodefeciency virus (HIV) infections in the USA, yet they represent less than 1 percent of the population [6]

  • Studies attempting to explain this disparity have shown that both Aboriginal men and women are at an increased risk of antecedent risk factors for HIV infection including sexual abuse, a history of IDU, poverty, poor mental health and involvement in the sex trade [7,8,9] within risk groups, for example amongst individuals with a history of injection drug use (IDU), Aboriginal men [10,11] and women [11,12] are at a higher risk of being infected with HIV

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Summary

Introduction

There are trends for global health concerns to have a greater impact on ethnic minorities [1,2,3,4,5]. In addition to a higher risk of HIV infection, it has been shown that Aboriginal persons were more likely to suffer from other morbidities that can complicate HIV disease progression. HIV-infected Aboriginal youths, were more likely to be co-infected with hepatitis C virus [13,14,15], being depressed [16,17], and having anemia [18], all of which have been independently associated with morbidity or mortality in HIV-infected individuals [19,20,21]. 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

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