Apolipoprotein-E genotype and human immunodeficiency virus-associated neurocognitive disorder: the modulating effects of older age and disease severity
Received 25 October 2012
Accepted for publication 24 December 2012
Published 19 June 2013 Volume 2013:5 Pages 11—22
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Stella E Panos,1,2 Charles H Hinkin,1,2 Elyse J Singer,3 April D Thames,1,2 Sapna M Patel,1,2 Janet S Sinsheimer,4 AC Del Re,5 Benjamin B Gelman,6 Susan Morgello,7 David J Moore,8 Andrew J Levine3
1Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, David Geffen School of Medicine, 2VA Greater Los Angeles Healthcare System; 3National Neurological AIDS Bank, UCLA Department of Neurology, 4Departments of Biomathematics and Human Genetics, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 5Department of Psychiatry, Stanford University, Menlo Park, CA, 6Department of Pathology, University of Texas Medical Branch, Galveston, TX, 7Departments of Neurology, Neuroscience, and Pathology, The Mount Sinai School of Medicine, New York, NY, 8Department of Psychiatry, School of Medicine, University of California San Diego, La Jolla, CA, USA
Background: The apolipoprotein-E (APOE) ε4 allele is a risk factor for vascular dementia and Alzheimer’s disease. Recent studies are equivocal with regards to whether or not the ε4 allele confers increased risk for the development of human immunodeficiency virus (HIV)-associated neurocognitive disorder (HAND), but suggest that age and/or disease severity may be modulating factors. The aim of this study was to assess the interactions and contributions of APOE genotype, age, and HIV disease severity as risk factors for HAND in HIV-infected adults.
Methods: Participants were 259 HIV-positive individuals who underwent APOE genotyping, a standardized neurological evaluation, a comprehensive neuropsychological evaluation, and laboratory testing.
Results: Older ε4 carriers showed a higher frequency of HAND compared with age-matched non-ε4 carriers. Analysis by discrete neurocognitive domain revealed that advanced age modulated the effect of the ε4 allele, such that older ε4 allele carriers showed reduced executive functioning and information processing speed. Exploratory analyses assessing the relationship between ε4 and disease severity in the overall sample revealed that disease severity modulated the effect of the ε4 allele on cognition. Lower absolute CD4+ cell count among ε4 allele carriers was associated with poorer working memory ability.
Conclusion: Advancing age and degree of immunosuppression may influence the association between APOE ε4 allele status and HAND. These two factors need to be taken into account in future research.
Keywords: apolipoprotein-E, human immunodeficiency virus, aging, neurocognition
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