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Published on: March 17, 2016
The joint effect of aging and HIV infection on microstructure of white matter bundles
Taylor Kuhn1, Yan Jin2,3, Chao Huang3
1Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, California.
Abstract:
Recent evidence suggests the aging process is accelerated by HIV. Degradation of white matter (WM) has been independently associated with HIV and healthy aging. Thus, WM may be vulnerable to joint effects of HIV and aging. Diffusion-weighted imaging (DWI) was conducted with HIV-seropositive (n = 72) and HIV-seronegative (n = 34) adults. DWI data underwent tractography, which was parcellated into 18 WM tracts of interest (TOIs). Functional Analysis of Diffusion Tensor Tract Statistics (FADTTS) regression was conducted assessing the joint effect of advanced age and HIV on fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) along TOI fibers. In addition to main effects of age and HIV on WM microstructure, the interactive effect of age and HIV was significantly related to lower FA and higher MD, AD, and RD across all TOIs. The location of findings was consistent with the clinical presentation of HIV-associated neurocognitive disorders. While older age is related to poorer WM microstructure, its detrimental effect on WM is stronger among HIV+ relative to HIV- individuals. Loss of WM integrity in the context of advancing age may place HIV+ individuals at increased risk for brain and cognitive compromise.
Insights
HIV accelerates aging, particularly impacting white matter (WM) integrity. Advanced age combined with HIV significantly worsens WM microstructure, increasing brain and cognitive risks for HIV-positive individuals.
Area of Science:
- Neuroscience
- Infectious Diseases
- Gerontology
Background:
- The aging process may be accelerated by Human Immunodeficiency Virus (HIV).
- White matter (WM) degradation is independently linked to both HIV and healthy aging.
- WM integrity may be particularly vulnerable to the combined effects of HIV and aging.
Purpose of the Study:
- To investigate the joint effect of advanced age and HIV on white matter (WM) microstructure.
- To assess how aging and HIV interact to influence specific diffusion tensor imaging (DTI) metrics in WM tracts.
Main Methods:
- Diffusion-weighted imaging (DWI) was performed on HIV-seropositive (n=72) and HIV-seronegative (n=34) adults.
- Tractography was used to analyze DWI data, parcellating 18 white matter tracts of interest (TOIs).
- Functional Analysis of Diffusion Tensor Tract Statistics (FADTTS) regression assessed the interaction of age and HIV on fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD).
Main Results:
- Significant main effects of both age and HIV were observed on WM microstructure.
- A significant interactive effect of age and HIV was found, leading to lower FA and higher MD, AD, and RD across all analyzed WM tracts.
- The observed patterns of WM alterations align with the clinical presentation of HIV-associated neurocognitive disorders.
Conclusions:
- While older age negatively impacts WM microstructure, this detrimental effect is amplified in individuals with HIV.
- The combined effects of aging and HIV significantly compromise WM integrity.
- Loss of WM integrity in aging HIV+ individuals may elevate the risk for neurological and cognitive decline.
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