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ABSTRACT: Background
Our understanding of HIV-1 and antiretroviral treatment (ART) is strongly biased towards subtype B, the predominant subtype in North America and western Europe. Efforts to characterize the response to first-line treatments in other HIV-1 subtypes have been hindered by the availability of large study cohorts in resource-limited settings. To maximize our statistical power, we combined HIV-1 sequence and clinical data from every available study population associated with the Joint Clinical Research Centre (JCRC) in Uganda. These records were combined with contemporaneous ART-naive records from Uganda in the Stanford HIVdb database.Methods
Treatment failures were defined by the presence of HIV genotype records with sample collection dates after the ART start dates in
SUBMITTER: Poon AFY
PROVIDER: S-EPMC6343277 | biostudies-literature | 2019 Jan
REPOSITORIES: biostudies-literature