4.1 Article

Predictors of CNS injury as measured by proton magnetic resonance spectroscopy in the setting of chronic HIV infection and CART

Journal

JOURNAL OF NEUROVIROLOGY
Volume 20, Issue 3, Pages 294-303

Publisher

SPRINGER
DOI: 10.1007/s13365-014-0246-6

Keywords

MRS; HIV dementia; Neuroimaging; Antiretroviral therapies; HIV RNA; Biomarkers

Funding

  1. NCATS NIH HHS [UL1 TR001108, UL1 TR001082] Funding Source: Medline
  2. NCRR NIH HHS [RR025780, UL1 RR025780] Funding Source: Medline
  3. NIAAA NIH HHS [R00 AA020235] Funding Source: Medline
  4. NIAID NIH HHS [U01 AI069424, AI069424, UM1 AI069424] Funding Source: Medline
  5. NIA NIH HHS [P30 AG028740] Funding Source: Medline
  6. NIBIB NIH HHS [U54 EB020403] Funding Source: Medline
  7. NIMH NIH HHS [U01 MH083500, U24 MH100929, U01MH083506, R01 MH099921, U24 MH100928, MH083506, U01MH083500, U01 MH083506] Funding Source: Medline
  8. NINDS NIH HHS [R01 NS036524, NS038841, R24 NS038841, NS36524] Funding Source: Medline

Ask authors/readers for more resources

The reasons for persistent brain dysfunction in chronically HIV-infected persons on stable combined antiretroviral therapies (CART) remain unclear. Host and viral factors along with their interactions were examined in 260 HIV-infected subjects who underwent magnetic resonance spectroscopy (MRS). Metabolite concentrations (NAA/Cr, Cho/Cr, MI/Cr, and Glx/Cr) were measured in the basal ganglia, the frontal white matter, and gray matter, and the best predictive models were selected using a bootstrap-enhanced Akaike information criterion (AIC). Depending on the metabolite and brain region, age, race, HIV RNA concentration, ADC stage, duration of HIV infection, nadir CD4, and/or their interactions were predictive of metabolite concentrations, particularly the basal ganglia NAA/Cr and the mid-frontal NAA/Cr and Glx/Cr, whereas current CD4 and the CPE index rarely or did not predict these changes. These results show for the first time that host and viral factors related to both current and past HIV status contribute to persisting cerebral metabolite abnormalities and provide a framework for further understanding neurological injury in the setting of chronic and stable disease.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available