Rates of non-confounded HIV-associated neurocognitive disorders in men initiating combination antiretroviral therapy during primary infection
- PMID: 26684817
- PMCID: PMC4685724
- DOI: 10.1097/QAD.0000000000000892
Rates of non-confounded HIV-associated neurocognitive disorders in men initiating combination antiretroviral therapy during primary infection
Erratum in
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Rates of non-confounded HIV-associated neurocognitive disorders in men initiating combination antiretroviral therapy during primary infection: Erratum.AIDS. 2016 Jul 31;30(12):2005. doi: 10.1097/01.aids.0000490040.25335.5a. AIDS. 2016. PMID: 27434493 No abstract available.
Abstract
Objective: To determine the prevalence of HIV-associated neurocognitive disorders (HAND) in HIV-infected participants who initiated combination antiretroviral therapy (cART) during primary infection.
Design: Cross-sectional observational study.
Methods: HIV-infected men without neuropsychiatric confounds who had initiated cART during primary infection were administered a neuropsychological battery as well as questionnaires evaluating depression and quality of life. Eligibility was determined by a medical examination with history and review of records.
Results: Twenty-six primarily non-Hispanic white (73%), male (100%) participants were enrolled and underwent neurocognitive assessment. Mean age was 44 (28-71) years, with a median of 17 years of education (13-24). Median current and nadir CD4 T-cell counts were 828 (506-1411) and 359 (150-621) cells/μl. All participants had plasma HIV-1 RNA less than 50 copies/ml. Median duration of cART prior to enrolment was 5.7 years (2.2-9.9). Median global deficit score was 0.17 (0.00-0.60). Only one (4%) participant was impaired.
Conclusion: Rates of HAND in this cohort of HIV-infected men without comorbid conditions who initiated early cART are low. Our findings suggest a possible neuroprotective benefit of early cART and an important contribution of comorbidities to observed HAND prevalence.
Conflict of interest statement
M.M. is a paid consultant for Merck and Gilead. He receives grant support from Gilead and GlaxoSmithKline and is on the Speakers Bureau for Gilead and Bristol-Myers Squibb. The remaining authors have declared that no competing interests exist.
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