Our proposal is strengthened by our previous extensive experience with the measurement of cognitive impairment in advanced HIV/AIDS, especially those with a history of substance abuse. The proposal builds on the established NEAD cohort already participating in longitudinal studies of HIV-1 infection in Baltimore.
The specific aims are:
AIM 1 : To identify protein markers in CSF that can distinguish progressive from static HIV-associated neurocognitive disorders (HAND) in individuals with a history of substance abuse. Our hypothesis is that CSF protein markers will be able to differentiate the temporal progression of HAND, reflecting underlying pathophysiological processes, particularly the effects of oxidative stress.
AIM 2 : To identify protein markers in CSF that differentiate individuals who may be at high risk for the development of HAND because of an increased genetic vulnerability to oxidative stress. Our hypthesis is that CSF protein markers will show variability among individuals based on genetic differences in genes which may regulate host response to oxidative stress. This project relies on the careful, serial characterization of the neurocognitive status of individuals chronically infected with HIV-1. Detailed histories of substance abuse will be gathered so that we can fractionate the cohort by the patterns of drug use. We will also explore the role of genetic variability in the regulation of oxidative stress through our collaboration with Dr George Uhl, head of the Molecular Neurobiology group at NIDA. He has expertise in the areas of molecular neurobiology and complex genetics related to addiction

Public Health Relevance

HIV-associated neurocogntive disorders remain a prevalent condition affecting 30% of individuals chronically infected with HIV-1. This is despite the wider availability of HAART which can provide effective suppression of HIV. The essential features of HAND are disabling cognitive impairment, usually accompanied by motor dysfunction. We anticipate being able to identify protein markers that will serve as predictive markers for HAND, and allow for earlier identiification and improved treatments.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Exploratory Grants (P20)
Project #
5P20DA026164-02
Application #
8065420
Study Section
Special Emphasis Panel (ZDA1)
Project Start
Project End
Budget Start
2010-04-01
Budget End
2011-03-31
Support Year
2
Fiscal Year
2010
Total Cost
$33,226
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Saylor, Deanna; Dickens, Alex M; Sacktor, Ned et al. (2016) HIV-associated neurocognitive disorder--pathogenesis and prospects for treatment. Nat Rev Neurol 12:234-48
Tharakan, Ravi; Edwards, Nathan; Graham, David R M (2010) Data maximization by multipass analysis of protein mass spectra. Proteomics 10:1160-71