Parasagittal dural space hypertrophy and amyloid-β deposition in Alzheimer's disease

One of the pathological hallmarks of Alzheimer's and related diseases is the increased accumulation of protein amyloid-beta in the brain parenchyma. As such, recent studies have focused on characterizing protein and related clearance pathways involving perivascular flow of neurofluids, but human studies of these pathways are limited owing to limited methods for evaluating neurofluid circulation non-invasively in vivo. Here, we utilize non-invasive MRI methods to explore surrogate measures of CSF production, bulk flow and egress in the context of independent PET measures of amyloid-beta accumulation in older adults. Participants (N = 23) were scanned at 3.0 T with 3D T-2-weighted turbo spin echo, 2D perfusion-weighted pseudo-continuous arterial spin labelling and phase-contrast angiography to quantify parasagittal dural space volume, choroid plexus perfusion and net CSF flow through the aqueduct of Sylvius, respectively. All participants also underwent dynamic PET imaging with amyloid-beta tracer C-11-Pittsburgh Compound B to quantify global cerebral amyloid-beta accumulation. Spearman's correlation analyses revealed a significant relationship between global amyloid-beta accumulation and parasagittal dural space volume (rho = 0.529, P = 0.010), specifically in the frontal (rho = 0.527, P = 0.010) and parietal (rho = 0.616, P = 0.002) subsegments. No relationships were observed between amyloid-beta and choroid plexus perfusion nor net CSF flow. Findings suggest that parasagittal dural space hypertrophy, and its possible role in CSF-mediated clearance, may be closely related to global amyloid-beta accumulation. These findings are discussed in the context of our growing understanding of the physiological mechanisms of amyloid-beta aggregation and clearance via neurofluids.