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Ashenagar, B.

Publications and source records attributed to Ashenagar, B..

2 recordsLinked to original sources

Modeling dynamic inflow effects in fMRI to quantify cerebrospinal fluid flow

Cerebrospinal fluid (CSF) flow in the brain is tightly regulated and essential for brain health, and imaging techniques are needed to quantitatively establish the properties of this flow system. Flow-sensitive fMRI has recently emerged as a tool to measure large scale CSF flow dynamics with high sensitivity and temporal resolution; however, the measured signal is not quantitative. Here, we developed a dynamic model to simulate fMRI inflow signals based on time-varying flow velocities. We validated the model in both human and phantom data, and used it to identify important properties of the fMRI inflow signal that inform how the signal should be interpreted. Additionally, we developed a physics-based deep learning framework to invert the model, which enables direct estimation of velocity using fMRI inflow data. This work allows new quantitative information to be obtained from fMRI, which will enable neuroimaging researchers to take advantage of the high sensitivity, high temporal resolution, and wide availability of fMRI to obtain flow signals that are physically interpretable.

neuroscience↗

The aging human brain exhibits reduced cerebrospinal fluid flow during sleep due to both neural and vascular factors

Aging reduces the quality and quantity of sleep, and greater sleep loss over the lifespan is predictive of neurodegeneration and cognitive decline. One mechanism by which sleep loss could contribute to impaired brain health is through disruption of cerebrospinal fluid (CSF) circulation. CSF is the primary waste transport system of the brain, and in young adults, CSF waves are largest during NREM sleep. However, whether sleep-dependent brain fluid physiology changes in aging is not known, due to the technical challenges of performing neuroimaging studies during sleep. We collected simultaneous fast fMRI and EEG data to measure large-scale CSF flow in healthy young and older adults and tested whether there were age-related changes to CSF dynamics during nighttime sleep. We found that sleep-dependent CSF flow was reduced in older adults, and this reduction was linked to impaired frontal EEG delta power and global hemodynamic oscillations during sleep. To identify mechanisms underlying reduced CSF flow, we used sensory and vasoactive stimuli to drive CSF flow in daytime task experiments, and found that both neural and cerebrovascular physiological changes contributed to the disruption of CSF flow during sleep. Finally, we found that this reduction in CSF flow was associated with gray matter atrophy in aging. Together, these results demonstrate that the aging human brain has reduced CSF flow during sleep, and identifies underlying neurovascular mechanisms that contribute to this age-related decline, suggesting targets for future interventions.

neuroscience↗