Factors related to HIV-associated neurocognitive impairment differ with age

Journal of NeuroVirology - Tập 21 - Trang 56-65 - 2014
Gary B. Fogel1, Susanna L. Lamers2, Andrew J. Levine3,4, Miguel Valdes-Sueiras3,4, Michael S. McGrath5,6, Paul Shapshak7, Elyse J. Singer3,4
1Natural Selection Inc., San Diego, USA
2Bioinfoexperts, LLC, Thibodaux, USA
3Department of Neurology, David Geffen School of Medicine at University of California, Los Angeles, USA
4National Neurological AIDS Bank, Los Angeles, USA
5Department of Laboratory Medicine, University of California, San Francisco, San Francisco, USA
6AIDS and Cancer Specimen Resource, San Francisco, USA
7Division of Infectious Diseases and International Medicine, Department of Psychiatry and Behavioral Medicine, University of South Florida College of Medicine, Tampa, USA

Tóm tắt

Over 50 % of HIV-infected (HIV+) persons are expected to be over age 50 by 2015. The pathogenic effects of HIV, particularly in cases of long-term infection, may intersect with those of age-related illnesses and prolonged exposure to combined antiretroviral therapy (cART). One potential outcome is an increased prevalence of neurocognitive impairment in older HIV+ individuals, as well as an altered presentation of HIV-associated neurocognitive disorders (HANDs). In this study, we employed stepwise regression to examine 24 features sometimes associated with HAND in 40 older (55–73 years of age) and 30 younger (32–50 years of age) HIV+, cART-treated participants without significant central nervous system confounds. The features most effective in generating a true assessment of the likelihood of HAND diagnosis differed between older and younger cohorts, with the younger cohort containing features associated with drug abuse that were correlated to HAND and the older cohort containing features that were associated with lipid disorders mildly associated with HAND. As the HIV-infected population grows and the demographics of the epidemic change, it is increasingly important to re-evaluate features associated with neurocognitive impairment. Here, we have identified features, routinely collected in primary care settings, that provide more accurate diagnostic value than a neurocognitive screening measure among younger and older HIV individuals.

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