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Detecting Altered connectivity patterns in HIV associated neurocognitive impairment using Mutual Connectivity
Anas Zainul Abidin1, Adora M D'Souza2, Mahesh B Nagarajan1
1Departments of Imaging Sciences & Biomedical Engineering, University of Rochester, New York, United States.
This study introduces Mutual Connectivity Analysis (MCA) to detect brain network differences in HIV infection. HIV+ individuals showed significantly decreased connectivity, particularly in basal ganglia regions, impacting cognitive function.
Area of Science:
- Neuroimaging
- Neurology
- Network Science
Background:
- Functional Magnetic Resonance Imaging (fMRI) reveals brain network changes in neurological disorders.
- HIV infection often leads to cognitive deficits, known as HIV-associated neurocognitive disorder (HAND).
Purpose of the Study:
- To apply a novel Mutual Connectivity Analysis (MCA) technique to detect brain network differences between HIV-positive and HIV-negative individuals.
- To investigate the utility of MCA combined with Network-Based Statistics (NBS) in a clinical case-control setting.
Main Methods:
- Resting-state fMRI data from 10 subjects (5 HIV+, 5 HIV-) were pre-processed.
- Mutual Connectivity Analysis (MCA) was used to generate brain network graphs from Automated Anatomic Labeling (AAL) atlas data.
- Network-Based Statistics (NBS) compared graph edges between groups, controlling for family-wise error rate.
Main Results:
- A significantly different network (42 nodes, 65 edges) was identified between HIV+ and HIV- subjects.
- HIV+ individuals exhibited decreased connectivity in basal ganglia regions and affected posterior cingulate cortex nodes.
- Findings align with existing knowledge of HIV-associated neurocognitive disorder (HAND) pathophysiology.
Conclusions:
- The novel MCA approach, coupled with NBS, effectively detects connectivity pattern differences in clinical populations.
- This method holds promise for understanding brain network alterations in HIV infection and HAND.
- The study highlights significant network disruptions in HIV+ individuals, particularly involving the basal ganglia.
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