Reductions in Gray Matter Linked to Epigenetic HIV-Associated Accelerated Aging
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Published on: March 23, 2011
Brandon J Lew1,2, Mikki D Schantell1, Jennifer O'Neill3
1Institute for Human Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.
Abstract:
A growing literature suggests a relationship between HIV-infection and a molecular profile of age acceleration. However, despite the widely known high prevalence of HIV-related brain atrophy and HIV-associated neurocognitive disorder (HAND), epigenetic age acceleration has not been linked to HIV-related changes in structural MRI. We applied morphological MRI methods to study the brain structure of 110 virally suppressed participants with HIV infection and 122 uninfected controls age 22-72. All participants were assessed for cognitive impairment, and blood samples were collected from a subset of 86 participants with HIV and 83 controls to estimate epigenetic age. We examined the group-level interactive effects of HIV and chronological age and then used individual estimations of epigenetic age to understand the relationship between age acceleration and brain structure. Finally, we studied the effects of HAND. HIV-infection was related to gray matter reductions, independent of age. However, using epigenetic age as a biomarker for age acceleration, individual HIV-related age acceleration was associated with reductions in total gray matter. HAND was associated with decreases in thalamic and hippocampal gray matter. In conclusion, despite viral suppression, accentuated gray matter loss is evident with HIV-infection, and greater biological age acceleration specifically relates to such gray matter loss.
Insights
HIV infection accelerates biological aging, leading to accelerated gray matter loss in the brain, even with viral suppression. This age acceleration is linked to reduced brain matter, impacting individuals with HIV.
Area of Science:
- Neuroscience
- Immunology
- Genetics
Background:
- HIV infection is associated with accelerated aging and neurocognitive deficits.
- Epigenetic age acceleration has not been previously linked to structural brain changes in HIV.
Purpose of the Study:
- To investigate the relationship between HIV infection, epigenetic age acceleration, and brain structure using MRI.
- To examine the impact of HIV and age acceleration on gray matter volume and cognitive function.
Main Methods:
- Morphological MRI was used to analyze brain structure in virally suppressed individuals with HIV and uninfected controls.
- Epigenetic age was estimated from blood samples to assess biological age acceleration.
- Cognitive function was assessed, and the effects of HIV-associated neurocognitive disorder (HAND) were studied.
Main Results:
- HIV infection was independently associated with reduced gray matter volume.
- Individual HIV-related age acceleration correlated with decreased total gray matter.
- HIV-associated neurocognitive disorder (HAND) was linked to reductions in thalamic and hippocampal gray matter.
Conclusions:
- Despite viral suppression, HIV infection leads to accelerated gray matter loss.
- Greater biological age acceleration is specifically associated with this gray matter loss in HIV.
- Epigenetic age acceleration serves as a biomarker for age-related brain changes in HIV.
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