4.1 Article

No association between Apoε4 alleles, HIV infection, age, neuropsychological outcome, or death

Journal

JOURNAL OF NEUROVIROLOGY
Volume 21, Issue 1, Pages 24-31

Publisher

SPRINGER
DOI: 10.1007/s13365-014-0290-2

Keywords

HIV disease; ApoE; Cognition; Age

Funding

  1. AIDS Cohort Study (MACS) with centers at Baltimore [U01-AI35042]
  2. Johns Hopkins University Bloomberg School of Public Health
  3. Feinberg School of Medicine
  4. Northwestern University
  5. Cook County Bureau of Health Services
  6. University of California
  7. UCLA Schools of Public Health and Medicine
  8. Zuo Feng Zhang
  9. Pittsburgh [U01-AI35041]
  10. University of Pittsburgh
  11. Graduate School of Public Health
  12. James T. Becker, Ross D. Cranston, Jeremy J. Martinson, John W. Mellors, Anthony J. Silvestre, Ronald D. Stall
  13. Data Coordinating Center [UM1-AI35043]
  14. National Institute of Allergy and Infectious Diseases (NIAID)
  15. National Cancer Institute (NCI)
  16. National Heart, Lung, and Blood Institute (NHLBI)
  17. National Institute on Deafness and Communication Disorders (NIDCD)
  18. NIH [AG034852, MH098745]
  19. [U01-AI35039]
  20. [U01-AI35040]
  21. [UL1-TR000424 (JHU CTSA)]

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The epsilon 4 allele of the apolipoprotein E (ApoE) gene may have important interactions with physical health and cognitive function among individuals with HIV disease. The purpose of this study is to examine the relationships between epsilon 4, HIV disease, age, neuropsychological impairment, and death in a large, well-characterized study sample. A total of 2846 men participating in the Multicenter AIDS Cohort Study had ApoE genotyping and neuropsychological test data available for analysis. We found a significant association between HIV infection and time to death (from any cause), as well as older age, race, and education. But, ApoE status was not significantly associated with time to death. Similarly, we found a significant association between HIV infection and time to incident cognitive impairment, as well as age, education, and HIV serostatus; Apo epsilon 4 status was not related to incident cognitive impairment. There were no significant interactions between ApoE, HIV infection, and age on cognitive impairment. These data replicate and strengthen prior findings of the lack of association between ApoE epsilon 4 and cognitive outcomes in HIV disease. We conclude that within the specific constraints of an exclusively male study in which the majority of participants were less than 65 years of age (range 22-87 years), it appears reasonable to conclude that the epsilon 4 allele is not significantly interacting with HIV serostatus.

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