Volumetric distribution of perivascular space in relation to mild cognitive impairment

Neurobiol Aging. 2021 Mar:99:28-43. doi: 10.1016/j.neurobiolaging.2020.12.010. Epub 2020 Dec 16.

Abstract

Vascular contributions to early cognitive decline are increasingly recognized, prompting further investigation into the nature of related changes in perivascular spaces (PVS). Using magnetic resonance imaging, we show that, compared to a cognitively normal sample, individuals with early cognitive dysfunction have altered PVS presence and distribution, irrespective of Amyloid-β. Surprisingly, we noted lower PVS presence in the anterosuperior medial temporal lobe (asMTL) (1.29 times lower PVS volume fraction in cognitively impaired individuals, p < 0.0001), which was associated with entorhinal neurofibrillary tau tangle deposition (beta (standard error) = -0.98 (0.4); p = 0.014), one of the hallmarks of early Alzheimer's disease pathology. We also observed higher PVS volume fraction in centrum semi-ovale of the white matter, but only in female participants (1.47 times higher PVS volume fraction in cognitively impaired individuals, p = 0.0011). We also observed PVS changes in participants with history of hypertension (higher in the white matter and lower in the asMTL). Our results suggest that anatomically specific alteration of the PVS is an early neuroimaging feature of cognitive impairment in aging adults, which is differentially manifested in female.

Keywords: Alzheimer’s disease; Clearance system; Cognitive decline; Perivascular space.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / pathology
  • Amyloid / metabolism
  • Cognitive Dysfunction / pathology*
  • Female
  • Glymphatic System / diagnostic imaging
  • Glymphatic System / metabolism
  • Glymphatic System / pathology*
  • Humans
  • Hypertension / pathology
  • Magnetic Resonance Imaging
  • Male
  • Neurofibrillary Tangles / metabolism
  • Neuroimaging
  • Organ Size
  • Sex Characteristics
  • White Matter / pathology
  • tau Proteins / metabolism

Substances

  • Amyloid
  • tau Proteins