Cannabis use impacts pre-stimulus neural activity in the visual cortices of people with HIV

People with HIV (PWH) use cannabis at a higher rate than the general population, but the influence on neural activity is not well characterized. Cannabis use among PWH may have a beneficial effect, as neuroinflammation is known to be a critical problem in PWH and cannabis use has been associated wit...

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Bibliographic Details
Main Authors: Christopher-Hayes, N.J (Author), Lew, B.J (Author), May, P.E (Author), O'Neill, J. (Author), Schantell, M. (Author), Swindells, S. (Author), Wiesman, A.I (Author), Wilson, T.W (Author)
Format: Article
Language:English
Published: John Wiley and Sons Inc 2021
Subjects:
MEG
Online Access:View Fulltext in Publisher
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001 10.1002-hbm.25634
008 220427s2021 CNT 000 0 und d
020 |a 10659471 (ISSN) 
245 1 0 |a Cannabis use impacts pre-stimulus neural activity in the visual cortices of people with HIV 
260 0 |b John Wiley and Sons Inc  |c 2021 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1002/hbm.25634 
520 3 |a People with HIV (PWH) use cannabis at a higher rate than the general population, but the influence on neural activity is not well characterized. Cannabis use among PWH may have a beneficial effect, as neuroinflammation is known to be a critical problem in PWH and cannabis use has been associated with a reduction in proinflammatory markers. Thus, it is important to understand the net impact of cannabis use on brain and cognitive function in PWH. In this study, we collected magnetoencephalographic (MEG) brain imaging data on 81 participants split across four demographically matched groups (i.e., PWH using cannabis, controls using cannabis, non-using PWH, and non-using controls). Participants completed a visuospatial processing task during MEG. Time–frequency resolved voxel time series were extracted to identify the dynamics of oscillatory and pre-stimulus baseline neural activity. Our results indicated strong theta (4–8 Hz), alpha (10–16 Hz), and gamma (62–72 Hz) visual oscillations in parietal–occipital brain regions across all participants. PWH exhibited significant behavioral deficits in visuospatial processing, as well as reduced theta oscillations and elevated pre-stimulus gamma activity in visual cortices, all of which replicate prior work. Strikingly, chronic cannabis use was associated with a significant reduction in pre-stimulus gamma activity in the visual cortices, such that PWH no longer statistically differed from controls. These results provide initial evidence that cannabis use may normalize some neural aberrations in PWH. This study fills an important gap in understanding the impact of cannabis use on brain and cognitive function in PWH. © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. 
650 0 4 |a adult 
650 0 4 |a Adult 
650 0 4 |a Article 
650 0 4 |a brain function 
650 0 4 |a brain region 
650 0 4 |a Brain Waves 
650 0 4 |a cannabinoid receptor affecting agent 
650 0 4 |a Cannabinoid Receptor Modulators 
650 0 4 |a cannabis 
650 0 4 |a cannabis addiction 
650 0 4 |a cannabis use 
650 0 4 |a CD4 antigen 
650 0 4 |a cognition 
650 0 4 |a cognitive defect 
650 0 4 |a Cognitive Dysfunction 
650 0 4 |a complication 
650 0 4 |a controlled study 
650 0 4 |a depth perception 
650 0 4 |a drug effect 
650 0 4 |a electroencephalogram 
650 0 4 |a false positive result 
650 0 4 |a female 
650 0 4 |a Female 
650 0 4 |a gamma 
650 0 4 |a HIV Infections 
650 0 4 |a human 
650 0 4 |a Human immunodeficiency virus 
650 0 4 |a Human immunodeficiency virus infection 
650 0 4 |a Human immunodeficiency virus infection 
650 0 4 |a Humans 
650 0 4 |a magnetoencephalography 
650 0 4 |a magnetoencephalography 
650 0 4 |a magnetoencephalography 
650 0 4 |a Magnetoencephalography 
650 0 4 |a major clinical study 
650 0 4 |a male 
650 0 4 |a Male 
650 0 4 |a medical cannabis 
650 0 4 |a Medical Marijuana 
650 0 4 |a MEG 
650 0 4 |a middle aged 
650 0 4 |a Middle Aged 
650 0 4 |a molecular dynamics 
650 0 4 |a nerve cell 
650 0 4 |a nerve potential 
650 0 4 |a neural oscillations 
650 0 4 |a neurocognitive decline 
650 0 4 |a neuropsychological test 
650 0 4 |a nuclear magnetic resonance imaging 
650 0 4 |a oscillation 
650 0 4 |a parietal cortex 
650 0 4 |a pathophysiology 
650 0 4 |a physiology 
650 0 4 |a stimulus response 
650 0 4 |a task performance 
650 0 4 |a time series analysis 
650 0 4 |a vision 
650 0 4 |a visual cortex 
650 0 4 |a Visual Cortex 
650 0 4 |a Visual Perception 
650 0 4 |a visuospatial processing 
650 0 4 |a visuospatial processing task 
700 1 |a Christopher-Hayes, N.J.  |e author 
700 1 |a Lew, B.J.  |e author 
700 1 |a May, P.E.  |e author 
700 1 |a O'Neill, J.  |e author 
700 1 |a Schantell, M.  |e author 
700 1 |a Swindells, S.  |e author 
700 1 |a Wiesman, A.I.  |e author 
700 1 |a Wilson, T.W.  |e author 
773 |t Human Brain Mapping